Trial Outcomes & Findings for Comparative Efficacy and Safety Study of GP2015 and Enbrel® in Patients With Rheumatoid Arthritis (NCT NCT02638259)
NCT ID: NCT02638259
Last Updated: 2018-09-19
Results Overview
Disease activity score (DAS) 28-CRP is based on 28-joint count (tender and swollen joints), C-reactive protein and patient's assessment of global disease activity, values range from 0.96 to 10.0 while higher values mean a higher disease activity. • A DAS28-CRP value \>5.1 corresponds to a high disease activity • A DAS28-CRP value between 3.2 and 5.1 corresponds to a moderate disease activity • A DAS28-CRP value between 2.6 and 3.2 corresponds to a low disease activity • A DAS28-CRP value \< 2.6 corresponds to remission DAS28-CRP = 0.56 \* sqrt(tender28) + 0.28\* sqrt(swollen28) + 0.36 \* ln(CRP+1) + 0.014 \* GDA + 0.96 where • tender28 and swollen28 are the number of tender and swollen joints as assessed using 28-joint count • CRP is C-reactive protein (mg/l) • GDA is the global disease activity measured on a Visual Analogue Scale (VAS) of 100 mm
COMPLETED
PHASE3
376 participants
treatment period 1: up to 24 weeks
2018-09-19
Participant Flow
Participant milestones
| Measure |
50mg GP2015
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
Group 2 will receive treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response will be switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1
STARTED
|
186
|
190
|
|
Treatment Period 1
COMPLETED
|
181
|
172
|
|
Treatment Period 1
NOT COMPLETED
|
5
|
18
|
|
Treatment Period 2
STARTED
|
175
|
166
|
|
Treatment Period 2
COMPLETED
|
169
|
155
|
|
Treatment Period 2
NOT COMPLETED
|
6
|
11
|
Reasons for withdrawal
| Measure |
50mg GP2015
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
Group 2 will receive treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response will be switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1
Adverse Event
|
1
|
5
|
|
Treatment Period 1
Death
|
0
|
1
|
|
Treatment Period 1
Lack of Efficacy
|
0
|
1
|
|
Treatment Period 1
Protocol Violation
|
0
|
3
|
|
Treatment Period 1
Withdrawal by Subject
|
4
|
6
|
|
Treatment Period 1
Withdrawn per sponsor decision
|
0
|
2
|
|
Treatment Period 2
Adverse Event
|
5
|
4
|
|
Treatment Period 2
Withdrawal by Subject
|
1
|
7
|
Baseline Characteristics
Comparative Efficacy and Safety Study of GP2015 and Enbrel® in Patients With Rheumatoid Arthritis
Baseline characteristics by cohort
| Measure |
50mg GP2015
n=186 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=190 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
Total
n=376 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
55.2 years
STANDARD_DEVIATION 11.22 • n=99 Participants
|
53.1 years
STANDARD_DEVIATION 12.70 • n=107 Participants
|
54.1 years
STANDARD_DEVIATION 12.02 • n=206 Participants
|
|
Sex: Female, Male
Female
|
158 Participants
n=99 Participants
|
150 Participants
n=107 Participants
|
308 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
28 Participants
n=99 Participants
|
40 Participants
n=107 Participants
|
68 Participants
n=206 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
1 Participants
n=99 Participants
|
1 Participants
n=107 Participants
|
2 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=99 Participants
|
3 Participants
n=107 Participants
|
3 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Black or African American
|
5 Participants
n=99 Participants
|
1 Participants
n=107 Participants
|
6 Participants
n=206 Participants
|
|
Race (NIH/OMB)
White
|
180 Participants
n=99 Participants
|
185 Participants
n=107 Participants
|
365 Participants
n=206 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
0 Participants
n=206 Participants
|
|
Region of Enrollment
Hungary
|
7 Participants
n=99 Participants
|
12 Participants
n=107 Participants
|
19 Participants
n=206 Participants
|
|
Region of Enrollment
United States
|
23 Participants
n=99 Participants
|
26 Participants
n=107 Participants
|
49 Participants
n=206 Participants
|
|
Region of Enrollment
Czechia
|
16 Participants
n=99 Participants
|
15 Participants
n=107 Participants
|
31 Participants
n=206 Participants
|
|
Region of Enrollment
United Kingdom
|
3 Participants
n=99 Participants
|
4 Participants
n=107 Participants
|
7 Participants
n=206 Participants
|
|
Region of Enrollment
Spain
|
5 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
10 Participants
n=206 Participants
|
|
Region of Enrollment
Russia
|
12 Participants
n=99 Participants
|
10 Participants
n=107 Participants
|
22 Participants
n=206 Participants
|
|
Region of Enrollment
Latvia
|
6 Participants
n=99 Participants
|
2 Participants
n=107 Participants
|
8 Participants
n=206 Participants
|
|
Region of Enrollment
Poland
|
44 Participants
n=99 Participants
|
48 Participants
n=107 Participants
|
92 Participants
n=206 Participants
|
|
Region of Enrollment
Italy
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
|
Region of Enrollment
Mexico
|
4 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
9 Participants
n=206 Participants
|
|
Region of Enrollment
Slovakia
|
3 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
8 Participants
n=206 Participants
|
|
Region of Enrollment
Bulgaria
|
11 Participants
n=99 Participants
|
11 Participants
n=107 Participants
|
22 Participants
n=206 Participants
|
|
Region of Enrollment
Lithuania
|
9 Participants
n=99 Participants
|
12 Participants
n=107 Participants
|
21 Participants
n=206 Participants
|
|
Region of Enrollment
Serbia
|
12 Participants
n=99 Participants
|
10 Participants
n=107 Participants
|
22 Participants
n=206 Participants
|
|
Region of Enrollment
Germany
|
4 Participants
n=99 Participants
|
5 Participants
n=107 Participants
|
9 Participants
n=206 Participants
|
|
Region of Enrollment
Estonia
|
26 Participants
n=99 Participants
|
20 Participants
n=107 Participants
|
46 Participants
n=206 Participants
|
PRIMARY outcome
Timeframe: treatment period 1: up to 24 weeksPopulation: Treatment Period 1 Per-Protocol set
Disease activity score (DAS) 28-CRP is based on 28-joint count (tender and swollen joints), C-reactive protein and patient's assessment of global disease activity, values range from 0.96 to 10.0 while higher values mean a higher disease activity. • A DAS28-CRP value \>5.1 corresponds to a high disease activity • A DAS28-CRP value between 3.2 and 5.1 corresponds to a moderate disease activity • A DAS28-CRP value between 2.6 and 3.2 corresponds to a low disease activity • A DAS28-CRP value \< 2.6 corresponds to remission DAS28-CRP = 0.56 \* sqrt(tender28) + 0.28\* sqrt(swollen28) + 0.36 \* ln(CRP+1) + 0.014 \* GDA + 0.96 where • tender28 and swollen28 are the number of tender and swollen joints as assessed using 28-joint count • CRP is C-reactive protein (mg/l) • GDA is the global disease activity measured on a Visual Analogue Scale (VAS) of 100 mm
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Safety: Change in DAS28-CRP Score From Baseline to Week 24 in Patients Treated With GP2015 and Patients Treated With Enbrel
|
-2.80 scores on a scale
Standard Error 0.113
|
-2.73 scores on a scale
Standard Error 0.117
|
SECONDARY outcome
Timeframe: Treatment Period 1, up to 24 weeksPopulation: Safety Set
Frequency of participants with injection site reactions in GP2015 and Enbrel
Outcome measures
| Measure |
50mg GP2015
n=186 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=190 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1: Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
All injection site reactions
|
13 Participants
|
35 Participants
|
|
Treatment Period 1: Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
Moderate injection site reactions
|
1 Participants
|
5 Participants
|
|
Treatment Period 1: Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
Severe injection site reactions
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: baseline, week 2, week 4, week 12, week 24Population: Safety Set
Frequency of patients having anti-drug antibody (ADA) during 24 weeks (Treatment Period 1) using 1% false positive rate
Outcome measures
| Measure |
50mg GP2015
n=186 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=190 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Safety : Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 2
|
2 Participants
|
5 Participants
|
|
Treatment Period 1 - Safety : Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 4
|
3 Participants
|
42 Participants
|
|
Treatment Period 1 - Safety : Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Baseline
|
2 Participants
|
0 Participants
|
|
Treatment Period 1 - Safety : Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 12
|
0 Participants
|
5 Participants
|
|
Treatment Period 1 - Safety : Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 24
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: week 4, 12, 24Population: Treatment period 1 per protocol set. Patients with data available
DAS28-CRP is a disease activity score and defined in primary outcome measure. DAS28-ESR is the DAS28 erythrocyte sedimentation rate score. DAS28-CRP and DAS28-ESR: 1. best is 0, 2. \< 2.6 - remission, 3. ≥ 2.6 to ≤ 3.2 - low disease activity 4. \> 3.2 to ≤ 5.1 - moderate disease activity 5. \> 5.1 - high disease activity DAS28-ESR = 0.56 \* sqrt(tender28) + 0.28\* sqrt(swollen28) + 0.7 \* ln(ESR) + 0.014 \* GDA where • tender28 and swollen28 are the number of tender and swollen joints as assessed using 28-joint count • CRP is C-reactive protein (mg/l) • ESR is erythrocyte sedimentation rate (mm/h) • GDA is the global disease activity measured on a Visual Analogue Scale (VAS) of 100 mm
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-CRP week 4
|
3.81 score on a scale
Standard Deviation 1.079
|
3.82 score on a scale
Standard Deviation 1.077
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-CRP baseline
|
5.42 score on a scale
Standard Deviation 0.921
|
5.53 score on a scale
Standard Deviation 0.783
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-CRP week 12
|
3.15 score on a scale
Standard Deviation 1.045
|
3.31 score on a scale
Standard Deviation 1.088
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-CRP week 24
|
2.63 score on a scale
Standard Deviation 0.910
|
2.75 score on a scale
Standard Deviation 0.928
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-ESR baseline
|
6.34 score on a scale
Standard Deviation 0.882
|
6.41 score on a scale
Standard Deviation 0.768
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-ESR week 4
|
4.62 score on a scale
Standard Deviation 1.183
|
4.56 score on a scale
Standard Deviation 1.204
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-ESR week 12
|
3.84 score on a scale
Standard Deviation 1.216
|
3.94 score on a scale
Standard Deviation 1.284
|
|
Treatment Period 1- DAS28-CRP and DAS28-erythrocyte Sedimentation Rate (ESR) Scores at Baseline and Weeks 4, 12 and 24;
DAS28-ESR week 24
|
3.24 score on a scale
Standard Deviation 1.060
|
3.32 score on a scale
Standard Deviation 1.099
|
SECONDARY outcome
Timeframe: baseline, Week 4, week 12, week 24Population: Treatment period 1 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-CRP change from baseline week 4
|
-1.59 score on a scale
Standard Deviation 1.032
|
-1.70 score on a scale
Standard Deviation 1.001
|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-CRP change from baseline week 12
|
-2.23 score on a scale
Standard Deviation 1.030
|
-2.20 score on a scale
Standard Deviation 1.071
|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-CRP change from baseline week 24
|
-2.78 score on a scale
Standard Deviation 1.058
|
-2.78 score on a scale
Standard Deviation 1.028
|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-ESR change from baseline week 4
|
-1.72 score on a scale
Standard Deviation 1.068
|
-1.85 score on a scale
Standard Deviation 1.078
|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-ESR change from baseline week 12
|
-2.50 score on a scale
Standard Deviation 1.145
|
-2.47 score on a scale
Standard Deviation 1.218
|
|
Treatment Period 1 - Changes From Baseline in DAS28-CRP and DAS-ESR Scores to Weeks 4, 12 and 24
DAS28-ESR change from baseline week 24
|
-3.10 score on a scale
Standard Deviation 1.157
|
-3.09 score on a scale
Standard Deviation 1.119
|
SECONDARY outcome
Timeframe: week 4, week 12 and week 24Population: Treatment period 1 per protocol set. Patients with data available
Proportion of patients achieving European League against Rheumatism (EULAR) good response (defined as DAS28 ≤ 3.2 and DAS28 improvement from Baseline \> 1.2) and moderate response (defined as DAS28 ≤ 3.2 and DAS28 improvement \> 0.6 and ≤ 1.2, or DAS28 \> 3.2 and ≤ 5.1 and DAS28 improvement \> 0.6 or DAS28 \> 5.1 but DAS28 improvement \> 1.2) ;
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Good response week 24
|
88 Participants
|
74 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Good response week 4
|
26 Participants
|
21 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Good response week 12
|
54 Participants
|
47 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Moderate response week 4
|
95 Participants
|
99 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Moderate response week 12
|
103 Participants
|
91 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
Moderate response week 24
|
76 Participants
|
77 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
no response week 4
|
46 Participants
|
34 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
no response week 12
|
11 Participants
|
16 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR Response
no response week 24
|
4 Participants
|
4 Participants
|
SECONDARY outcome
Timeframe: week 4, week 12 and week 24Population: Treatment period 1 per protocol set. Patients with data available
% patients in DAS28-ESR categories up to week 24
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- Proportion of Patients Achieving DAS28 < 2.6 at Weeks 4, 12 and 24
Week 24 - remission (DAS28 <2.6)
|
46 Participants
|
41 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving DAS28 < 2.6 at Weeks 4, 12 and 24
Week 4 - remission (DAS28 <2.6)
|
9 Participants
|
7 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving DAS28 < 2.6 at Weeks 4, 12 and 24
Week 12 - remission (DAS28 <2.6)
|
21 Participants
|
21 Participants
|
SECONDARY outcome
Timeframe: week 4, week 12, week 24Population: Treatment period 1 per protocol set. Patients with data available
Proportion of patients achieving EULAR/American College of Rheumatology (EULAR/ACR) Boolean remission criteria (defined as number of tender joints/swollen joints ≤ 1 and CRP (mg/dL) ≤ 1 and patient global assessment (1-10) ≤ 1) at Weeks 4, 12 and 24;
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
week 24
|
24 Participants
|
15 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
week 4
|
1 Participants
|
2 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
week 12
|
9 Participants
|
8 Participants
|
SECONDARY outcome
Timeframe: Week 4, week 12 and week 24Population: Treatment period 1 per protocol set. Patients with data available
ACR20 response was defined if a patient fulfilled all 3 criteria below: * 20% improvement in tender 68 joint-count * 20% improvement in swollen 68 joint-count; And 20% improvement in at least 3 of the following 5 measures: * Patient's assessment of RA pain (visual analogue scale (VAS) 100 mm), * Patient's global assessment of disease activity (VAS 100 mm), * Physician's global assessment of disease activity (VAS 100 mm), * Patient self-assessed disability (HAQ score), * Acute phase reactant (CRP or ESR). ACR50 and ACR70 responses were defined as ACR20 response replacing "20% improvement" by "50% improvement" and "70% improvement", respectively.
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR20 response Week 4
|
80 Participants
|
83 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR20 response Week 24
|
147 Participants
|
144 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR50 response Week 4
|
25 Participants
|
28 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR50 response Week 12
|
55 Participants
|
68 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR50 response Week 24
|
107 Participants
|
110 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR70 response Week 4
|
8 Participants
|
7 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR70 response Week 12
|
21 Participants
|
26 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR20 response Week 12
|
131 Participants
|
116 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving ACR20/50/70 Response at Weeks 4, 12 and 24;
ACR70 response Week 24
|
56 Participants
|
66 Participants
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
ACR-N (American College of Rheumatology percentage of improvement): negative is worsening, positive (up to 100) is an improvement. ACR-N is a single number that characterizes the percentage of improvement from Baseline that a patient has experienced in analogy to ACR20 described above. ACR-N of X (such as 38) means that the patient had achieved an improvement of at least X% (such as 38%) in tender and swollen joints, and an improvement of at least X% (such as 38%) in 3 of the 5 other parameters mentioned above.
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- ACR-N Scores at Weeks 4, 12 and 24;
week 4
|
19.9 score on a scale
Standard Deviation 29.89
|
22.6 score on a scale
Standard Deviation 34.02
|
|
Treatment Period 1- ACR-N Scores at Weeks 4, 12 and 24;
week 12
|
38.3 score on a scale
Standard Deviation 27.46
|
38.7 score on a scale
Standard Deviation 35.32
|
|
Treatment Period 1- ACR-N Scores at Weeks 4, 12 and 24;
week 24
|
55.4 score on a scale
Standard Deviation 27.61
|
59.4 score on a scale
Standard Deviation 25.40
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
Proportion of patients in each disease activity category as defined by the Simplified Disease Activity Index (SDAI): high disease activity, SDAI \> 26, moderate disease activity, SDAI \> 11 to ≤ 26, low disease activity, SDAI \> 3.3 to ≤ 11, and remission, SDAI ≤ 3.3 at Weeks 4, 12 and 24; SDAI and CDAI are measures of disease activity in RA. The scores were calculated by numerical summation of the number of tender and swollen joints (using the 28-joint count), and the patient's and physician's global assessment of disease activity.
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4:High (SDAI > 26)
|
41 Participants
|
36 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12:Remission (SDAI<=3.3)
|
15 Participants
|
13 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline: Low (3.3 < SDAI <= 11)
|
0 Participants
|
0 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : Moderate (11 < SDAI <= 26
|
26 Participants
|
19 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : High (SDAI > 26)
|
142 Participants
|
136 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4:Remission (SDAI<=3.3)
|
5 Participants
|
4 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12:Low (3.3 < SDAI <= 11)
|
61 Participants
|
58 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12: Moderate (11 < SDAI <= 26
|
75 Participants
|
68 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12:High (SDAI > 26)
|
14 Participants
|
11 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24: Remission (SDAI<=3.3)
|
38 Participants
|
31 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24: Low (3.3 < SDAI <= 11)
|
83 Participants
|
81 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24 : Moderate (11 < SDAI <= 26
|
45 Participants
|
38 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24 :High (SDAI > 26)
|
2 Participants
|
5 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : Remission (SDAI<=3.3)
|
0 Participants
|
0 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4:Low (3.3 < SDAI <= 11)
|
35 Participants
|
31 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4: Moderate (11 < SDAI <= 26
|
84 Participants
|
82 Participants
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
Proportion of patients in each disease activity category as defined by the Clinical Disease Activity Index (CDAI): high disease activity, CDAI \> 22, moderate disease activity, CDAI \> 10 to ≤ 22, low disease activity, CDAI \> 2.8 to ≤ 10, and remission, CDAI ≤ 2.8 at Weeks 4, 12 and 24; SDAI and CDAI are measures of disease activity in RA. The scores were calculated by numerical summation of the number of tender and swollen joints (using the 28-joint count), and the patient's and physician's global assessment of disease activity.
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : Remission (CDAI<=2.8)
|
0 Participants
|
0 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12:High (CDAI > 22)
|
19 Participants
|
23 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12: Low (2.8 < CDAI <= 10)
|
63 Participants
|
53 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12: Moderate (10 < CDAI <= 22)
|
72 Participants
|
63 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline: Low (2.8 < CDAI <= 10)
|
0 Participants
|
0 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : Moderate (10 < CDAI <= 22
|
17 Participants
|
7 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : High (CDAI > 22)
|
151 Participants
|
148 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4:Remission(CDAI<=2.8)
|
4 Participants
|
3 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4: Low (2.8 < CDAI <= 10)
|
33 Participants
|
31 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4: Moderate (10 < CDAI <= 22)
|
67 Participants
|
71 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4:High High (CDAI > 22)
|
63 Participants
|
49 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12:Remission(CDAI<=2.8)
|
14 Participants
|
15 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24: Remission (CDAI<=2.8)
|
35 Participants
|
31 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24: Low (2.8 < CDAI <= 10)
|
81 Participants
|
78 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24 : (10 < CDAI <= 22)
|
46 Participants
|
39 Participants
|
|
Treatment Period 1 - Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24 :High (CDAI > 22)
|
6 Participants
|
7 Participants
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
Health assessment questionnaire (HAQ) disability index ranges from 0 (best) to 3 (worst)
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1- Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 4, 12 and 24;
Baseline
|
11 Participants
|
5 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 4, 12 and 24;
Week 4
|
22 Participants
|
30 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 4, 12 and 24;
Week 12
|
40 Participants
|
46 Participants
|
|
Treatment Period 1- Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 4, 12 and 24;
Week 24
|
54 Participants
|
62 Participants
|
SECONDARY outcome
Timeframe: Baseline, Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
Health assessment questionnaire (HAQ) disability index ranges from 0 (best) to 3 (worst)
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Health Assessment Questionnaire (HAQ) Index at Baseline, Weeks 4, 12 and 24;
Week 12
|
1.02 score on a scale
Standard Deviation 0.560
|
0.97 score on a scale
Standard Deviation 0.599
|
|
Treatment Period 1 - Health Assessment Questionnaire (HAQ) Index at Baseline, Weeks 4, 12 and 24;
Baseline
|
1.44 score on a scale
Standard Deviation 0.547
|
1.47 score on a scale
Standard Deviation 0.561
|
|
Treatment Period 1 - Health Assessment Questionnaire (HAQ) Index at Baseline, Weeks 4, 12 and 24;
Week 4
|
1.19 score on a scale
Standard Deviation 0.558
|
1.14 score on a scale
Standard Deviation 0.611
|
|
Treatment Period 1 - Health Assessment Questionnaire (HAQ) Index at Baseline, Weeks 4, 12 and 24;
Week 24
|
0.88 score on a scale
Standard Deviation 0.601
|
0.80 score on a scale
Standard Deviation 0.589
|
SECONDARY outcome
Timeframe: Baseline, Weeks 4, 12 and 24;Population: Treatment period 1 per protocol set. Patients with data available
FACIT fatigue scale is a 13- item questionnaire that assesses self-reported fatigue and its impact upon daily activities and function, ranging from 0 (worst) to 52 (best). A score of less than 30 indicates severe fatigue.
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 4, 12 and 24;
Baseline
|
27.0 score on a scale
Standard Deviation 9.67
|
25.1 score on a scale
Standard Deviation 10.33
|
|
Treatment Period 1 - Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 4, 12 and 24;
Week 4
|
31.6 score on a scale
Standard Deviation 8.83
|
30.9 score on a scale
Standard Deviation 10.01
|
|
Treatment Period 1 - Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 4, 12 and 24;
Week 12
|
34.4 score on a scale
Standard Deviation 8.93
|
33.9 score on a scale
Standard Deviation 9.6
|
|
Treatment Period 1 - Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 4, 12 and 24;
Week 24
|
36.3 score on a scale
Standard Deviation 8.94
|
36.7 score on a scale
Standard Deviation 9.24
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24Population: Treatment period 1 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - CRP Levels at Baseline and Weeks 4, 12 and 24
Baseline
|
1.19 mg/dL
Standard Deviation 2.194
|
1.10 mg/dL
Standard Deviation 1.526
|
|
Treatment Period 1 - CRP Levels at Baseline and Weeks 4, 12 and 24
Week 4
|
0.36 mg/dL
Standard Deviation 0.718
|
0.43 mg/dL
Standard Deviation 0.693
|
|
Treatment Period 1 - CRP Levels at Baseline and Weeks 4, 12 and 24
Week 12
|
0.33 mg/dL
Standard Deviation 0.772
|
0.48 mg/dL
Standard Deviation 0.850
|
|
Treatment Period 1 - CRP Levels at Baseline and Weeks 4, 12 and 24
Week 24
|
0.44 mg/dL
Standard Deviation 0.949
|
0.35 mg/dL
Standard Deviation 0.466
|
SECONDARY outcome
Timeframe: Weeks 4, 12 and 24Population: Treatment period 1 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=168 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=155 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 1 - ESR Levels at Baseline and Weeks 4, 12 and 24
Baseline
|
41.4 mm/h
Standard Deviation 16.89
|
41.8 mm/h
Standard Deviation 17.94
|
|
Treatment Period 1 - ESR Levels at Baseline and Weeks 4, 12 and 24
Week 4
|
26.5 mm/h
Standard Deviation 16.51
|
26.7 mm/h
Standard Deviation 17.27
|
|
Treatment Period 1 - ESR Levels at Baseline and Weeks 4, 12 and 24
Week 12
|
23.2 mm/h
Standard Deviation 14.67
|
23.8 mm/h
Standard Deviation 15.41
|
|
Treatment Period 1 - ESR Levels at Baseline and Weeks 4, 12 and 24
Week 24
|
21.4 mm/h
Standard Deviation 15.47
|
20.8 mm/h
Standard Deviation 14.05
|
SECONDARY outcome
Timeframe: Baseline, week 4, week 12, week 24, week 36 and week 48.Population: Treatment period 2 per protocol set. Patients with data available
DAS28-CRP and DAS28-ESR: 1. best is 0, 2. \< 2.6 - remission, 3. ≥ 2.6 to ≤ 3.2 - low disease activity 4. \> 3.2 to ≤ 5.1 - moderate disease activity 5. \> 5.1 - high disease activity
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Week 4
|
4.70 score on a scale
Standard Deviation 1.175
|
4.49 score on a scale
Standard Deviation 1.228
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Week 12
|
3.90 score on a scale
Standard Deviation 1.236
|
3.85 score on a scale
Standard Deviation 1.317
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Week 24
|
3.23 score on a scale
Standard Deviation 1.022
|
3.19 score on a scale
Standard Deviation 1.048
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Baseline
|
5.45 score on a scale
Standard Deviation 0.914
|
5.57 score on a scale
Standard Deviation 0.794
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Week 4
|
3.89 score on a scale
Standard Deviation 1.053
|
3.79 score on a scale
Standard Deviation 1.101
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Week 12
|
3.20 score on a scale
Standard Deviation 1.038
|
3.27 score on a scale
Standard Deviation 1.127
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Week 24
|
2.64 score on a scale
Standard Deviation 0.863
|
2.67 score on a scale
Standard Deviation 0.892
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Week 36
|
2.65 score on a scale
Standard Deviation 1.001
|
2.74 score on a scale
Standard Deviation 1.017
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-CRP Week 48
|
2.57 score on a scale
Standard Deviation 1.067
|
2.74 score on a scale
Standard Deviation 1.062
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Baseline
|
6.39 score on a scale
Standard Deviation 0.872
|
6.43 score on a scale
Standard Deviation 0.784
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Week 36
|
3.25 score on a scale
Standard Deviation 1.160
|
3.28 score on a scale
Standard Deviation 1.127
|
|
Treatment Period 2: DAS28-CRP and DAS28-ESR Scores up to Week 48;
DAS28-ESR Week 48
|
3.20 score on a scale
Standard Deviation 1.201
|
3.30 score on a scale
Standard Deviation 1.177
|
SECONDARY outcome
Timeframe: week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-CRP change from baseline, week 4
|
-1.55 score on a scale
Standard Deviation 1.014
|
-1.76 score on a scale
Standard Deviation 1.014
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-CRP change from baseline, week 12
|
-2.22 score on a scale
Standard Deviation 1.031
|
-2.27 score on a scale
Standard Deviation 1.096
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-CRP change from baseline, week 24
|
-2.81 score on a scale
Standard Deviation 1.007
|
-2.90 score on a scale
Standard Deviation 0.988
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-CRP change from baseline, week 36
|
-2.80 score on a scale
Standard Deviation 1.087
|
-2.82 score on a scale
Standard Deviation 1.151
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-CRP change from baseline, week 48
|
-2.88 score on a scale
Standard Deviation 1.198
|
-2.83 score on a scale
Standard Deviation 1.176
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-ESR change from baseline, week 4
|
-1.69 score on a scale
Standard Deviation 1.048
|
-1.92 score on a scale
Standard Deviation 1.087
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-ESR change from baseline, week 12
|
-2.49 score on a scale
Standard Deviation 1.152
|
-2.57 score on a scale
Standard Deviation 1.235
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-ESR change from baseline, week 24
|
-3.16 score on a scale
Standard Deviation 1.106
|
-3.23 score on a scale
Standard Deviation 1.054
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-ESR change from baseline, week 36
|
-3.13 score on a scale
Standard Deviation 1.232
|
-3.14 score on a scale
Standard Deviation 1.154
|
|
Treatment Period 2 : Changes From Baseline in DAS28-CRP and DAS28-ESR Scores From Week 4 up to Week 48
DAS28-ESR change from baseline, week 48
|
-3.20 score on a scale
Standard Deviation 1.297
|
-3.14 score on a scale
Standard Deviation 1.190
|
SECONDARY outcome
Timeframe: week 4, week 12, week 24, week 36 and week 48Population: Treatment period 2 per protocol set. Patients with data available
Proportion of patients achieving EULAR good response (defined as DAS28 ≤ 3.2 and DAS28 improvement from Baseline \> 1.2) and moderate response (defined as DAS28 ≤ 3.2 and DAS28 improvement \> 0.6 and ≤ 1.2, or DAS28 \> 3.2 and ≤ 5.1 and DAS28 improvement \> 0.6 or DAS28 \> 5.1 but DAS28 improvement \> 1.2) at Weeks 36 and 48;
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Good response week 4
|
20 Participants
|
20 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Good response week 12
|
43 Participants
|
43 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Good response week 24
|
77 Participants
|
68 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Good response week 36
|
82 Participants
|
65 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Good response week 48
|
80 Participants
|
67 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Moderate response week 4
|
85 Participants
|
82 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Moderate response week 12
|
95 Participants
|
75 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Moderate response week 24
|
71 Participants
|
63 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Moderate response week 36
|
62 Participants
|
64 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
Moderate response week 48
|
61 Participants
|
57 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
no response week 4
|
42 Participants
|
28 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
no response week 12
|
10 Participants
|
12 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
no response week 24
|
0 Participants
|
0 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
no response week 36
|
3 Participants
|
2 Participants
|
|
Treatment Period 2: Proportion of Patients Achieving EULAR Reponse
no response week 48
|
6 Participants
|
5 Participants
|
SECONDARY outcome
Timeframe: week 36 and week 48Population: Treatment period 2 per protocol set. Patients with data available
percentage of participants in DAS28-ESR categories up to week 48
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Proportion of Patients Achieving DAS28 < 2.6 at Weeks 36 and 48;
Week 36 Remission (DAS28 < 2.6)
|
45 Participants
|
38 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving DAS28 < 2.6 at Weeks 36 and 48;
Week 48 Remission (DAS28 < 2.6)
|
44 Participants
|
35 Participants
|
SECONDARY outcome
Timeframe: week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
Proportion of patients achieving EULAR/ACR Boolean remission criteria (defined as number of tender joints/swollen joints ≤ 1 and CRP (mg/dL) ≤ 1 and patient global assessment (1-10) ≤ 1) at Weeks 36 and 48;
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
Week 4
|
0 Participants
|
2 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
Week 12
|
9 Participants
|
8 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
Week 24
|
22 Participants
|
13 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
Week 36
|
25 Participants
|
15 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving EULAR/ACR Boolean Remission Criteria
Week 48
|
28 Participants
|
20 Participants
|
SECONDARY outcome
Timeframe: week 36 and week 48Population: Treatment period 2 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR20 response Week 36
|
128 Participants
|
114 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR20 response Week 48
|
131 Participants
|
108 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR50 response Week 36
|
90 Participants
|
83 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR50 response Week 48
|
93 Participants
|
86 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR70 response Week 36
|
47 Participants
|
50 Participants
|
|
Treatment Period 2 : Proportion of Patients Achieving ACR20/50/70 Response at Weeks 36 and 48;
ACR70 response Week 48
|
54 Participants
|
55 Participants
|
SECONDARY outcome
Timeframe: week 36 and week 48Population: Treatment period 2 per protocol set. Patients with data available
ACR-N: negative is worsening, positive (up to 100) is an improvement
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : ACR-N Scores at Weeks 36 and 48;
Week 4
|
19.7 score on a scale
Standard Deviation 27.72
|
24.9 score on a scale
Standard Deviation 29.40
|
|
Treatment Period 2 : ACR-N Scores at Weeks 36 and 48;
Week 12
|
38.3 score on a scale
Standard Deviation 27.84
|
40.7 score on a scale
Standard Deviation 34.80
|
|
Treatment Period 2 : ACR-N Scores at Weeks 36 and 48;
Week 24
|
56.3 score on a scale
Standard Deviation 26.58
|
60.9 score on a scale
Standard Deviation 24.79
|
|
Treatment Period 2 : ACR-N Scores at Weeks 36 and 48;
Week 36
|
53.8 score on a scale
Standard Deviation 28.21
|
55.7 score on a scale
Standard Deviation 28.37
|
|
Treatment Period 2 : ACR-N Scores at Weeks 36 and 48;
Week 48
|
56.9 score on a scale
Standard Deviation 29.18
|
56.4 score on a scale
Standard Deviation 30.58
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36. week 48Population: Treatment period 2 per protocol set. Patients with data available
Proportion of patients in each disease activity category as defined by the Simplified Disease Activity Index (SDAI): high disease activity, SDAI \> 26, moderate disease activity, SDAI \> 11 to ≤ 26, low disease activity, SDAI \> 3.3 to ≤ 11, and remission, SDAI ≤ 3.3 at Weeks 36 and 48.
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4 : Moderate (11 < SDAI <= 26
|
75 Participants
|
69 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4 : High (SDAI > 26 )
|
39 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12: Remission (SDAI <= 3.3)
|
14 Participants
|
12 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12 : Low (3.3 < SDAI <= 11)
|
50 Participants
|
51 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12 : Moderate (11 < SDAI <= 26
|
69 Participants
|
53 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 12 : High (SDAI > 26 )
|
13 Participants
|
11 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24: Remission (SDAI <= 3.3)
|
31 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24 : Low (3.3 < SDAI <= 11)
|
74 Participants
|
71 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : Remission (SDAI <= 3.3)
|
0 Participants
|
0 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : Low (3.3 < SDAI <= 11)
|
0 Participants
|
0 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : Moderate (11 < SDAI <= 26)
|
20 Participants
|
16 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Baseline : High (SDAI > 26 )
|
128 Participants
|
115 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4 : Remission (SDAI <= 3.3)
|
2 Participants
|
4 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 4 : Low (3.3 < SDAI <= 11)
|
29 Participants
|
27 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24 : Moderate (11 < SDAI <= 26
|
43 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 24 : High (SDAI > 26 )
|
0 Participants
|
2 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 36: Remission (SDAI <= 3.3)
|
34 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 36 : Low (3.3 < SDAI <= 11
|
69 Participants
|
66 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 36 : Moderate (11 < SDAI <= 26
|
43 Participants
|
30 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 36 : High (SDAI > 26 )
|
1 Participants
|
5 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 48: Remission (SDAI <= 3.3)
|
39 Participants
|
32 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 48 : Low (3.3 < SDAI <= 11
|
72 Participants
|
62 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 48 : Moderate (11 < SDAI <= 26
|
30 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by SDAI
Week 48 : High (SDAI > 26 )
|
6 Participants
|
8 Participants
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36 and week 48Population: Treatment period 2 per protocol set. Patients with data available
Proportion of patients in each disease activity category as defined by the Clinical Disease Activity Index (CDAI): high disease activity, CDAI \> 22, moderate disease activity, CDAI \> 10 to ≤ 22, low disease activity, CDAI \> 2.8 to ≤ 10, and remission, CDAI ≤ 2.8 at Weeks 36 and 48;
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : High (CDAI > 22 )
|
134 Participants
|
125 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4 : Remission (CDAI <=2.8)
|
2 Participants
|
3 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 48 : High (CDAI > 22 )
|
7 Participants
|
8 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : Remission (CDAI <=2.8)
|
0 Participants
|
0 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : Low (2.8 < CDAI <= 10)
|
0 Participants
|
0 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Baseline : Moderate (10 < CDAI <= 22)
|
14 Participants
|
6 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4 : Low (2.8 < CDAI <= 10)
|
27 Participants
|
28 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4 : Moderate (11 < SDAI <= 26
|
60 Participants
|
60 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 4 : High (CDAI > 22 )
|
58 Participants
|
39 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12: Remission (CDAI <=2.8)
|
12 Participants
|
14 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12 : Low (2.8 < CDAI <= 10)
|
52 Participants
|
47 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12 : Moderate (10 < CDAI <= 22)
|
67 Participants
|
50 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 12 : High (CDAI > 22 )
|
17 Participants
|
19 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24: Remission (CDAI <=2.8)
|
29 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24 : Low (2.8 < CDAI <= 10)
|
71 Participants
|
68 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24 : Moderate (10 < CDAI <= 22)
|
45 Participants
|
30 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 24 : High (CDAI > 22 )
|
3 Participants
|
4 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 36: Remission (CDAI <=2.8)
|
32 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 36 : Low (2.8 < CDAI <= 10)
|
67 Participants
|
63 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 36 : Moderate (10 < CDAI <= 22)
|
41 Participants
|
32 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 36 : High (CDAI > 22 )
|
7 Participants
|
7 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 48: Remission (CDAI <=2.8)
|
37 Participants
|
29 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 48 : Low (2.8 < CDAI <= 10)
|
71 Participants
|
63 Participants
|
|
Treatment Period 2 : Proportion of Patients in Each Disease Activity Category as Defined by CDAI
Week 48 : Moderate (10 < CDAI <= 22)
|
32 Participants
|
31 Participants
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Baseline
|
8 Participants
|
4 Participants
|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Week 4
|
17 Participants
|
25 Participants
|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Week 12
|
33 Participants
|
39 Participants
|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Week 24
|
47 Participants
|
51 Participants
|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Week 36
|
46 Participants
|
48 Participants
|
|
Treatment Period 2 :Proportion of Patients Achieving HAQ Index in Normal Range (≤ 0.5) at Weeks 36 and 48;
Week 48
|
51 Participants
|
51 Participants
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
HAQ: from 0 (best) to 3 (worst)
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Baseline
|
1.47 score on a scale
Standard Deviation 0.547
|
1.50 score on a scale
Standard Deviation 0.554
|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Week 4
|
1.22 score on a scale
Standard Deviation 0.554
|
1.14 score on a scale
Standard Deviation 0.620
|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Week 12
|
1.04 score on a scale
Standard Deviation 0.560
|
0.97 score on a scale
Standard Deviation 0.614
|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Week 24
|
0.88 score on a scale
Standard Deviation 0.594
|
0.83 score on a scale
Standard Deviation 0.603
|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Week 36
|
0.89 score on a scale
Standard Deviation 0.584
|
0.85 score on a scale
Standard Deviation 0.651
|
|
Treatment Period 2 :HAQ Index at Weeks 36 and 48;
Week 48
|
0.85 score on a scale
Standard Deviation 0.609
|
0.84 score on a scale
Standard Deviation 0.652
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
FACIT: from 0 (worst) to 52 (best), a score of less than 30 indicates severe fatigue
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Baseline
|
26.6 score on a scale
Standard Deviation 9.71
|
25.5 score on a scale
Standard Deviation 10.78
|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Week 4
|
31.5 score on a scale
Standard Deviation 8.72
|
31.3 score on a scale
Standard Deviation 10.07
|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Week 12
|
34.4 score on a scale
Standard Deviation 8.89
|
34.1 score on a scale
Standard Deviation 9.69
|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Week 24
|
36.6 score on a scale
Standard Deviation 8.75
|
36.7 score on a scale
Standard Deviation 9.05
|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Week 36
|
36.9 score on a scale
Standard Deviation 8.79
|
36.4 score on a scale
Standard Deviation 9.50
|
|
Treatment Period 2 : Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale Relative to Baseline at Weeks 36 and 48;
Week 48
|
38.0 score on a scale
Standard Deviation 8.74
|
35.8 score on a scale
Standard Deviation 9.97
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Baseline
|
1.21 mg/dL
Standard Deviation 2.244
|
1.17 mg/dL
Standard Deviation 1.589
|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Week 4
|
0.36 mg/dL
Standard Deviation 0.733
|
0.42 mg/dL
Standard Deviation 0.625
|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Week 12
|
0.36 mg/dL
Standard Deviation 0.817
|
0.50 mg/dL
Standard Deviation 0.910
|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Week 24
|
0.44 mg/dL
Standard Deviation 0.964
|
0.36 mg/dL
Standard Deviation 0.487
|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Week 36
|
0.39 mg/dL
Standard Deviation 0.758
|
0.39 mg/dL
Standard Deviation 0.655
|
|
Treatment Period 2 : CRP Levels at Week 36 and 48
Week 48
|
0.35 mg/dL
Standard Deviation 0.623
|
0.40 mg/dL
Standard Deviation 0.878
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Treatment period 2 per protocol set. Patients with data available
Outcome measures
| Measure |
50mg GP2015
n=148 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=131 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Baseline
|
42.2 mm/h
Standard Deviation 16.99
|
41.7 mm/h
Standard Deviation 17.99
|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Week 4
|
26.8 mm/h
Standard Deviation 16.33
|
25.3 mm/h
Standard Deviation 16.11
|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Week 12
|
23.8 mm/h
Standard Deviation 15.07
|
23.0 mm/h
Standard Deviation 15.38
|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Week 24
|
21.3 mm/h
Standard Deviation 15.66
|
19.3 mm/h
Standard Deviation 12.66
|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Week 36
|
22.1 mm/h
Standard Deviation 16.41
|
20.3 mm/h
Standard Deviation 14.28
|
|
Treatment Period 2 : ESR Levels at Week 36 and 48
Week 48
|
22.8 mm/h
Standard Deviation 16.66
|
20.8 mm/h
Standard Deviation 14.62
|
SECONDARY outcome
Timeframe: up to 48 weeksPopulation: Safety Set
Frequency of participants with injection site reactions in GP2015 and Enbrel
Outcome measures
| Measure |
50mg GP2015
n=186 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=190 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Safety - Overall Study : Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
participants with at least one ISR
|
13 Participants
|
37 Participants
|
|
Safety - Overall Study : Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
participants with at least one moderate ISR
|
1 Participants
|
7 Participants
|
|
Safety - Overall Study : Frequency and Severity of Injection Site Reactions in GP2015 and Enbrel
participants with at least one severe ISR
|
0 Participants
|
0 Participants
|
SECONDARY outcome
Timeframe: baseline, week 4, week 12, week 24, week 36, week 48Population: Safety Set
To assess the immunogenicity of continuous GP2015 treatment versus a treatment transition from Enbrel to GP2015 after 24 weeks of treatment by measuring the rate of ADA positive participants at Weeks 24, 30, 36 and 48. summary of ADA positive data up to week 48 using a 1% false positive cut point
Outcome measures
| Measure |
50mg GP2015
n=186 Participants
Group 1 received treatment with 50mg GP2015 by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response continued treatment with 50mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
50mg EU-authorized Enbrel
n=190 Participants
Group 2 received treatment with 50mg EU-authorized Enbrel by subcutaneous injection every week up to 24 weeks (Treatment Period 1) after which patients achieving at least a moderate clinical response were switched to 50 mg GP2015 subcutaneous injection every week up to 48 weeks (Treatment Period 2). GP2015: Enbrel comparator
|
|---|---|---|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Baseline
|
2 Participants
|
0 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 2
|
2 Participants
|
5 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 4
|
3 Participants
|
42 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 12
|
0 Participants
|
5 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 24
|
0 Participants
|
0 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 30
|
2 Participants
|
0 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 36
|
0 Participants
|
0 Participants
|
|
Safety : Overall Study: Immunogenicity by Measuring the Rate of Anti-drug Antibody (ADA) Positive Patients
Week 48
|
2 Participants
|
0 Participants
|
Adverse Events
Treatment Period 1 TP1 SAF GP2015
Treatment Period 1 TP1 SAF Enbrel
Treatment Period 2 TP2 SAF Continued GP2015
Treatment Period 2 TP2 SAF Enbrel Switched to GP2015
Entire Study SAF GP2015
Entire Study SAF Enbrel/GP2015
Serious adverse events
| Measure |
Treatment Period 1 TP1 SAF GP2015
n=186 participants at risk
Treatment Period 1 TP1 SAF GP2015
|
Treatment Period 1 TP1 SAF Enbrel
n=190 participants at risk
Treatment Period 1 TP1 SAF Enbrel
|
Treatment Period 2 TP2 SAF Continued GP2015
n=175 participants at risk
Treatment Period 2 TP2 SAF Continued GP2015
|
Treatment Period 2 TP2 SAF Enbrel Switched to GP2015
n=166 participants at risk
Treatment Period 2 TP2 SAF Enbrel switched to GP2015
|
Entire Study SAF GP2015
n=186 participants at risk
Entire study SAF GP2015
|
Entire Study SAF Enbrel/GP2015
n=190 participants at risk
Entire study SAF Enbrel/GP2015
|
|---|---|---|---|---|---|---|
|
Cardiac disorders
Atrial fibrillation
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Cardiac disorders
Cardiac failure
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Gastrointestinal disorders
Salivary gland cyst
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.57%
1/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Hepatobiliary disorders
Cholecystitis acute
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Hepatobiliary disorders
Cholelithiasis
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Osteomyelitis
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Pneumonia
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.57%
1/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Injury, poisoning and procedural complications
Spinal fracture
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Injury, poisoning and procedural complications
Tibia fracture
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.57%
1/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Investigations
Hepatic enzyme increased
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Musculoskeletal and connective tissue disorders
Rheumatoid arthritis
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Breast cancer
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colon adenoma
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Lung neoplasm malignant
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Renal and urinary disorders
Cystitis haemorrhagic
|
0.00%
0/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.57%
1/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
Other adverse events
| Measure |
Treatment Period 1 TP1 SAF GP2015
n=186 participants at risk
Treatment Period 1 TP1 SAF GP2015
|
Treatment Period 1 TP1 SAF Enbrel
n=190 participants at risk
Treatment Period 1 TP1 SAF Enbrel
|
Treatment Period 2 TP2 SAF Continued GP2015
n=175 participants at risk
Treatment Period 2 TP2 SAF Continued GP2015
|
Treatment Period 2 TP2 SAF Enbrel Switched to GP2015
n=166 participants at risk
Treatment Period 2 TP2 SAF Enbrel switched to GP2015
|
Entire Study SAF GP2015
n=186 participants at risk
Entire study SAF GP2015
|
Entire Study SAF Enbrel/GP2015
n=190 participants at risk
Entire study SAF Enbrel/GP2015
|
|---|---|---|---|---|---|---|
|
Blood and lymphatic system disorders
Anaemia
|
1.1%
2/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Gastrointestinal disorders
Diarrhoea
|
1.6%
3/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.57%
1/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.2%
2/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
3.2%
6/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
General disorders
Injection site reaction
|
7.0%
13/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
18.4%
35/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
3.6%
6/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
7.0%
13/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
19.5%
37/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Bronchitis
|
1.1%
2/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.2%
2/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
3.2%
6/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Cystitis
|
1.1%
2/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.6%
5/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Nasopharyngitis
|
4.8%
9/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
7.4%
13/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
5.4%
9/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
9.7%
18/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
6.3%
12/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Pharyngitis
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.6%
3/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.60%
1/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.6%
3/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Upper respiratory tract infection
|
3.2%
6/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
3.7%
7/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
5.1%
9/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
5.4%
9/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
7.0%
13/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
7.9%
15/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Urinary tract infection
|
4.3%
8/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
4.2%
8/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
4.0%
7/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.2%
2/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
7.0%
13/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
4.2%
8/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Infections and infestations
Viral upper respiratory tract infection
|
1.1%
2/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.2%
2/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Investigations
Alanine aminotransferase increased
|
4.3%
8/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.1%
4/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.3%
4/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
3.6%
6/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
6.5%
12/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
4.2%
8/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Metabolism and nutrition disorders
Hyperuricaemia
|
1.6%
3/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Musculoskeletal and connective tissue disorders
Back pain
|
2.7%
5/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.7%
3/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
4.3%
8/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Nervous system disorders
Headache
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.53%
1/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.4%
4/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.54%
1/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.6%
5/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
|
Vascular disorders
Hypertension
|
1.1%
2/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/175 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
0.00%
0/166 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
2.2%
4/186 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
1.1%
2/190 • Adverse Events are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All Adverse events are reported in this record from First Patient First Treatment until Last Patient Last Visit up to approximately 1.5 years.
AE additional description
|
Additional Information
Sandoz Biopharma Clinical Development - Strategic Planning
Sandoz
Results disclosure agreements
- Principal investigator is a sponsor employee Terms related to publication are part of the contract templates between Sponsor and sites/investigators. In general, these terms outlined that authorship of any publications relating to the clinical study shall be determined by agreement with the Sponsor. Sponsor reserves the right to request amendments or deletions to proposed publications, or request that any publication or presentation be delayed up to four months. A very limited number of exceptions can be granted to modify these terms.
- Publication restrictions are in place
Restriction type: OTHER