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

Recruitment status

COMPLETED

Study phase

PHASE3

Target enrollment

376 participants

Primary outcome timeframe

treatment period 1: up to 24 weeks

Results posted on

2018-09-19

Participant Flow

Participant milestones

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

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

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 weeks

Population: 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

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 weeks

Population: Safety Set

Frequency of participants with injection site reactions in GP2015 and Enbrel

Outcome measures

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 24

Population: Safety Set

Frequency of patients having anti-drug antibody (ADA) during 24 weeks (Treatment Period 1) using 1% false positive rate

Outcome measures

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, 24

Population: 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

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 24

Population: Treatment period 1 per protocol set. Patients with data available

Outcome measures

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 24

Population: 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

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 24

Population: Treatment period 1 per protocol set. Patients with data available

% patients in DAS28-ESR categories up to week 24

Outcome measures

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 24

Population: 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

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 24

Population: 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

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

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

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

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

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

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

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 24

Population: Treatment period 1 per protocol set. Patients with data available

Outcome measures

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 24

Population: Treatment period 1 per protocol set. Patients with data available

Outcome measures

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

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 48

Population: Treatment period 2 per protocol set. Patients with data available

Outcome measures

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 48

Population: 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

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 48

Population: Treatment period 2 per protocol set. Patients with data available

percentage of participants in DAS28-ESR categories up to week 48

Outcome measures

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 48

Population: 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

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 48

Population: Treatment period 2 per protocol set. Patients with data available

Outcome measures

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 48

Population: Treatment period 2 per protocol set. Patients with data available

ACR-N: negative is worsening, positive (up to 100) is an improvement

Outcome measures

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 48

Population: 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

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 48

Population: 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

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 48

Population: Treatment period 2 per protocol set. Patients with data available

Outcome measures

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 48

Population: Treatment period 2 per protocol set. Patients with data available

HAQ: from 0 (best) to 3 (worst)

Outcome measures

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 48

Population: 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

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 48

Population: Treatment period 2 per protocol set. Patients with data available

Outcome measures

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 48

Population: Treatment period 2 per protocol set. Patients with data available

Outcome measures

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 weeks

Population: Safety Set

Frequency of participants with injection site reactions in GP2015 and Enbrel

Outcome measures

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 48

Population: 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

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

Serious events: 1 serious events
Other events: 52 other events
Deaths: 0 deaths

Treatment Period 1 TP1 SAF Enbrel

Serious events: 5 serious events
Other events: 64 other events
Deaths: 1 deaths

Treatment Period 2 TP2 SAF Continued GP2015

Serious events: 4 serious events
Other events: 42 other events
Deaths: 0 deaths

Treatment Period 2 TP2 SAF Enbrel Switched to GP2015

Serious events: 4 serious events
Other events: 37 other events
Deaths: 0 deaths

Entire Study SAF GP2015

Serious events: 5 serious events
Other events: 79 other events
Deaths: 0 deaths

Entire Study SAF Enbrel/GP2015

Serious events: 9 serious events
Other events: 81 other events
Deaths: 1 deaths

Serious adverse events

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

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

Phone: 0049(0)80244760

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