Trial Outcomes & Findings for Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic Arthritis in Patients With Psoriasis Severe or Moderate With Adalimumab Treatment (NCT NCT01316224)

NCT ID: NCT01316224

Last Updated: 2015-05-12

Results Overview

A participant is said to have PsA if they meet the following criteria: 1. PsA defined by a rheumatologist; or 2. A participant with inflamed joints \>0 and CASPAR score \>=3; or 3. Participant meeting at least one of the two previous definitions.

Recruitment status

COMPLETED

Target enrollment

52 participants

Primary outcome timeframe

At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Results posted on

2015-05-12

Participant Flow

Participant milestones

Participant milestones
Measure
Moderate or Severe Psoriasis
Participants with moderate or severe psoriasis in treatment with adalimumab
Overall Study
STARTED
52
Overall Study
Completed Visit 1 to Dermatologist
52
Overall Study
Completed Visit 1 to Rheumatologist
49
Overall Study
Completed Visit 2 to Dermatologist
51
Overall Study
Completed Visit 3 to Dermatologist
48
Overall Study
Completed Visit 3 to Rheumatologist
39
Overall Study
Completed Visit 4 to Dermatologist
42
Overall Study
Completed Visit 4 to Rheumatologist
28
Overall Study
COMPLETED
42
Overall Study
NOT COMPLETED
10

Reasons for withdrawal

Reasons for withdrawal
Measure
Moderate or Severe Psoriasis
Participants with moderate or severe psoriasis in treatment with adalimumab
Overall Study
Protocol Violation
3
Overall Study
Adverse Event
3
Overall Study
Lack of Efficacy
1
Overall Study
Withdrawal by Subject
1
Overall Study
Adverse Event With Treatment Failure
1
Overall Study
Other
1

Baseline Characteristics

Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic Arthritis in Patients With Psoriasis Severe or Moderate With Adalimumab Treatment

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Moderate or Severe Psoriasis
n=52 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Age, Continuous
48.85 Years
STANDARD_DEVIATION 14.66 • n=99 Participants
Sex: Female, Male
Female
21 Participants
n=99 Participants
Sex: Female, Male
Male
31 Participants
n=99 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
Race (NIH/OMB)
Asian
0 Participants
n=99 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=99 Participants
Race (NIH/OMB)
White
18 Participants
n=99 Participants
Race (NIH/OMB)
More than one race
34 Participants
n=99 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=99 Participants
Region of Enrollment
Colombia
52 Participants
n=99 Participants
Weight
78.70 kg
STANDARD_DEVIATION 14.70 • n=99 Participants
Body Mass Index (BMI)
28.83 kg/m^2
STANDARD_DEVIATION 5.06 • n=99 Participants
C-Reactive Protein (CRP) (N=10)
1.39 mg/dl
STANDARD_DEVIATION 1.63 • n=99 Participants
Study Specific Characteristic
Participants Who Smoke
21 Participants
n=99 Participants
Study Specific Characteristic
Positive History of Comorbidities
28 Participants
n=99 Participants
Study Specific Characteristic
Presence of Metabolic Syndrome
8 Participants
n=99 Participants
Study Specific Characteristic
Presence of Hypertension
15 Participants
n=99 Participants
Study Specific Characteristic
Presence of Family History of PsA (N=49)
11 Participants
n=99 Participants
Study Specific Characteristic
Prior Methotrexate Use
36 Participants
n=99 Participants
Study Specific Characteristic
Current Methotrexate Use
11 Participants
n=99 Participants
Study Specific Characteristic
Prior Biologic Therapy
14 Participants
n=99 Participants

PRIMARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

A participant is said to have PsA if they meet the following criteria: 1. PsA defined by a rheumatologist; or 2. A participant with inflamed joints \>0 and CASPAR score \>=3; or 3. Participant meeting at least one of the two previous definitions.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 1 - Visit 3 (N=38)
47.4 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 1 - Visit 4 (N=28)
35.7 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 2 - Baseline
17.3 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 2 - Visit 3 (N=39)
10.3 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 2 - Visit 4 (N=28)
3.6 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 3 - Visit 3 (N=39)
46.2 Percentage of participants
Percentage of Participants Who Developed Psoriatic Arthritis (PsA)
Definition 3 - Visit 4 (N=28)
35.7 Percentage of participants

PRIMARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

Signs or symptoms were defined as mentioning at the rheumatologist visit any joint symptoms prior to or during the visit or a total number of inflamed joints greater than 0.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants Who Developed Signs or Symptoms of PsA
Baseline
61.2 Percentage of participants
Percentage of Participants Who Developed Signs or Symptoms of PsA
Visit 3 (N=39)
33.3 Percentage of participants
Percentage of Participants Who Developed Signs or Symptoms of PsA
Visit 4 (N=28)
25.0 Percentage of participants

SECONDARY outcome

Timeframe: Baseline up to Visit 4 (month 12)

Population: Participants who completed at least one of the follow up visits to the rheumatologist.

The measure of time from Psoriasis diagnosis to the appearance of PsA signs or symptoms.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=44 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Mean Time to First Occurrence of PsA Signs or Symptoms
23.17 Years
Interval 16.33 to 30.01

SECONDARY outcome

Timeframe: At Baseline, Visit 2 (month 2), Visit 3 (month 6) and Visit 4 (month 12)

Population: ITT population

The PASI score was used to measure the severity of psoriasis. It combined the assessment of the severity of lesions and the area affected into a single score ranging from 0 (no disease) to 72 (maximal disease).

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=52 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Mean Change From Baseline in Psoriasis Area and Severity Index (PASI) Score
Change from Baseline at Visit 3 (N=47)
-13.12 PASI score
Standard Deviation 12.69
Mean Change From Baseline in Psoriasis Area and Severity Index (PASI) Score
Change from Baseline at Visit 4 (N=41)
-15.17 PASI score
Standard Deviation 12.69
Mean Change From Baseline in Psoriasis Area and Severity Index (PASI) Score
Baseline
17.42 PASI score
Standard Deviation 12.11
Mean Change From Baseline in Psoriasis Area and Severity Index (PASI) Score
Change from Baseline at Visit 2 (N=51)
-11.56 PASI score
Standard Deviation 11.96

SECONDARY outcome

Timeframe: Baseline up to Visit 4 (month 12)

Population: Participants who completed at least one of the follow up visits to the rheumatologist.

Percentage of participants with comorbidities (metabolic syndrome, hypertension, diabetes, atherosclerosis, obesity, alcohol and other associated comorbidities) was assessed.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=44 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants With Comorbidities Who Did or Did Not Develop PsA
Non-PsA participants (N=25)
60.0 Percentage of participants
Percentage of Participants With Comorbidities Who Did or Did Not Develop PsA
PsA participants (N=19)
52.6 Percentage of participants

SECONDARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: ITT population

The Short Form-36 was a self-reported questionnaire used to measure the QoL of participants in eight main health dimensions (physical functioning; bodily pain; role limitations due to physical health, personal, and emotional problems; emotional well-being; social functioning; vitality; and general health perception). The score from each health dimension was added together for a QoL score on a scale of 0 - 100; a higher score indicated a better QoL.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=52 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Mean Change in Quality of Life (QoL)
Physical Functioning (PF) at Baseline
78.46 Score on scale
Standard Deviation 28.66
Mean Change in Quality of Life (QoL)
Change from Baseline in PF at Visit 3 (N=47)
-1.52 Score on scale
Standard Deviation 25.80
Mean Change in Quality of Life (QoL)
Change from Baseline in PF at Visit 4 (N=47)
-0.95 Score on scale
Standard Deviation 24.92
Mean Change in Quality of Life (QoL)
Role-Physical (RP) at Baseline
68.75 Score on scale
Standard Deviation 26.89
Mean Change in Quality of Life (QoL)
Change from Baseline in RP at Visit 3 (N=47)
6.52 Score on scale
Standard Deviation 26.67
Mean Change in Quality of Life (QoL)
Change from Baseline in RP at Visit 4 (N=42)
6.55 Score on scale
Standard Deviation 35.16
Mean Change in Quality of Life (QoL)
Bodily Pain (BP) at Baseline (N=51)
66.78 Score on scale
Standard Deviation 29.73
Mean Change in Quality of Life (QoL)
Change from Baseline in BP at Visit 3 (N=47)
-0.87 Score on scale
Standard Deviation 32.08
Mean Change in Quality of Life (QoL)
Change from Baseline in BP at Visit 4 (N=42)
9.10 Score on scale
Standard Deviation 34.82
Mean Change in Quality of Life (QoL)
General Health (GH) at Baseline
57.88 Score on scale
Standard Deviation 23.55
Mean Change in Quality of Life (QoL)
Change from Baseline in GH at Visit 3 (N=46)
8.24 Score on scale
Standard Deviation 28.30
Mean Change in Quality of Life (QoL)
Change from Baseline in GH at Visit 4 (N=42)
12.95 Score on scale
Standard Deviation 31.45
Mean Change in Quality of Life (QoL)
Vitality at Baseline
60.58 Score on scale
Standard Deviation 24.37
Mean Change in Quality of Life (QoL)
Change from Baseline in vitality at Visit 3 (N=47)
2.13 Score on scale
Standard Deviation 24.18
Mean Change in Quality of Life (QoL)
Change from Baseline vitality at Visit 4 (N=42)
5.51 Score on scale
Standard Deviation 30.78
Mean Change in Quality of Life (QoL)
Social Functioning (SF) at Baseline
66.35 Score on scale
Standard Deviation 31.07
Mean Change in Quality of Life (QoL)
Change from Baseline in SF at Visit 3 (N=47)
13.56 Score on scale
Standard Deviation 29.24
Mean Change in Quality of Life (QoL)
Change from Baseline in SF at Visit 4 (N=42)
13.39 Score on scale
Standard Deviation 36.98
Mean Change in Quality of Life (QoL)
Role-Emotional (RE) at Baseline
68.11 Score on scale
Standard Deviation 28.47
Mean Change in Quality of Life (QoL)
Change from Baseline in RE at Visit 3 (N=47)
6.03 Score on scale
Standard Deviation 29.47
Mean Change in Quality of Life (QoL)
Change from Baseline in RE at Visit 4 (N=42)
15.67 Score on scale
Standard Deviation 34.05
Mean Change in Quality of Life (QoL)
Mental Health (MH) at Baseline
64.13 Score on scale
Standard Deviation 25.70
Mean Change in Quality of Life (QoL)
Change from Baseline in MH at Visit 3 (N=47)
6.28 Score on scale
Standard Deviation 24.33
Mean Change in Quality of Life (QoL)
Change from Baseline in MH at Visit 4 (N=42)
5.45 Score on scale
Standard Deviation 30.73

SECONDARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

The CASPAR criteria permits the diagnosis of PsA in spite of low rheumatoid factor positivity. To be classified as having PsA, a participant must have inflammatory articular disease (joint, spine, entheseal) with greater than or equal to 3 of the following 5 points: evidence of psoriasis (current, history of, or family history of); psoriatic nail dystrophy; a negative RF test result; dactylitis (history of or current); and radiographic evidence of juxa-articular new bone formation. Only current psoriasis (2 points) was weighted more heavily than the other features (1 point). CASPER scores range from 1 to 6, with 6 indicating a more definitive diagnosis of PsA.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Mean Change in ClASsification Criteria for Psoriatic ARthritis (CASPAR) Score
Baseline
2.82 CASPAR score
Standard Deviation 0.73
Mean Change in ClASsification Criteria for Psoriatic ARthritis (CASPAR) Score
Change from Baseline at Visit 3 (N=38)
0.05 CASPAR score
Standard Deviation 0.73
Mean Change in ClASsification Criteria for Psoriatic ARthritis (CASPAR) Score
Change from Baseline at Visit 4 (N=27)
-0.07 CASPAR score
Standard Deviation 0.83

SECONDARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

The CASPAR criteria permits the diagnosis of PsA in spite of low rheumatoid factor positivity. To be classified as having PsA, a participant must have inflammatory articular disease (joint, spine, entheseal) with greater than or equal to 3 of the following 5 points: evidence of psoriasis (current, history of, or family history of); psoriatic nail dystrophy; a negative RF test result; dactylitis (history of or current); and radiographic evidence of juxa-articular new bone formation. Only current psoriasis (2 points) was weighted more heavily than the other features (1 point).

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants With a CASPAR Score Greater Than or Equal to 3 at Each Visit to the Rheumatologist
Baseline
67.30 Percentage of participants
Percentage of Participants With a CASPAR Score Greater Than or Equal to 3 at Each Visit to the Rheumatologist
Visit 3 (N=39)
64.10 Percentage of participants
Percentage of Participants With a CASPAR Score Greater Than or Equal to 3 at Each Visit to the Rheumatologist
Visit 4 (N=28)
71.40 Percentage of participants

SECONDARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

Pressure and joint manipulation by physical examination on 68 or 66 joints or regions (34 or 32 per body side, hip joints excluded) were assessed for TJC or SJC, respectively. Both joint tenderness and swelling were classified as present ("1"), absent ("0"), replaced ("9"), or no assessment ("NA"). The total TJC or SJC was derived as the sum of the tender and swollen joints; the range for TJC and SJC was 0 - 68 and 0 - 66, respectively; with higher scores indicating worse conditions.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
SJC at Baseline
24.50 Percentage of participants
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
SJC at Visit 3 (N=39)
12.80 Percentage of participants
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
SJC at Visit 4 (N=28)
7.10 Percentage of participants
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
TJC at Baseline
36.70 Percentage of participants
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
TJC at Visit 3 (N=39)
20.50 Percentage of participants
Percentage of Participants With Swollen Joint Count (SJC) and Tender Joint Count (TJC) Greater Than Zero
TJC at Visit 4 (N=28)
14.30 Percentage of participants

SECONDARY outcome

Timeframe: At Baseline, Visit 3 (month 6) and Visit 4 (month 12)

Population: Participants who completed the visits (visit 3 and visit 4) to the rheumatologist and for whom information was available.

Joint symptoms were evaluated by presence or absence of peripheral arthritis, morning stiffness and participant reported joint symptoms.

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=49 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Percentage of Participants With Joint Symptoms
Baseline
61.20 Percentage of participants
Percentage of Participants With Joint Symptoms
Visit 3 (N=39)
30.80 Percentage of participants
Percentage of Participants With Joint Symptoms
Visit 4 (N=28)
25.00 Percentage of participants

SECONDARY outcome

Timeframe: Baseline up to Visit 4 (month 12)

Population: ITT population

The number of new PsA cases were determined by: 1. PsA defined by a rheumatologist; or 2. A participant with inflamed joints \>0 and CASPAR score \>=3; or 3. Participant meeting at least one of the two previous definitions occurring over person time (defined as the overall sum of Psoriasis disease duration without PsA).

Outcome measures

Outcome measures
Measure
Moderate or Severe Psoriasis
n=52 Participants
Participants with moderate or severe psoriasis in treatment with adalimumab
Incidence Rate of PsA Since Psoriasis Diagnosis
2.66 new PsA cases per 100 person years
Interval 1.7 to 4.14

SECONDARY outcome

Timeframe: At Baseline, Week 24, and Week 48

This outcome measure was not calculated.

Outcome measures

Outcome data not reported

Adverse Events

Moderate or Severe Psoriasis

Serious events: 16 serious events
Other events: 5 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Moderate or Severe Psoriasis
n=52 participants at risk
Participants with moderate or severe psoriasis in treatment with Adalimumab
Blood and lymphatic system disorders
Anemia
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Cardiac disorders
Myocardial infarction
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Ear and labyrinth disorders
Vertigo
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Gastrointestinal disorders
Abdominal pain
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Gastrointestinal disorders
Ascites
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Gastrointestinal disorders
Gastrointestinal haemorrhage
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
General disorders
Chest pain
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
General disorders
General physical health deterioration
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
General disorders
Localised oedema
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
General disorders
No therapeutic response
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
General disorders
Pain
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Hepatobiliary disorders
Hepatic steatosis
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Infections and infestations
Tonsillitis bacterial
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Investigations
Alpha 1 fetoprotein increased
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Investigations
Cardiac murmur
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Investigations
Liver function test abnormal
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Investigations
Transaminases increased
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Arthritis
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Dactylitis
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Muscle spasms
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Neck pain
3.8%
2/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Pain in extremity
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Musculoskeletal and connective tissue disorders
Psoriatic arthropathy
3.8%
2/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Hepatic cancer
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Melanocytic naevus
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Uterine leiomyoma
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Nervous system disorders
Headache
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Nervous system disorders
Syncope
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Psychiatric disorders
Bipolar I disorder
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Reproductive system and breast disorders
Breast calcifications
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Reproductive system and breast disorders
Mammary duct ectasia
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Reproductive system and breast disorders
Uterine haemorrhage
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Respiratory, thoracic and mediastinal disorders
Cough
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Respiratory, thoracic and mediastinal disorders
Dyspnea
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Respiratory, thoracic and mediastinal disorders
Pleural effusion
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Blister
3.8%
2/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Dermatosis
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Erythema
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Psoriasis
3.8%
2/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Rash generalized
3.8%
2/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Skin and subcutaneous tissue disorders
Toxic skin eruption
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Surgical and medical procedures
Mastectomy
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug
Vascular disorders
Hypertensive crisis
1.9%
1/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug

Other adverse events

Other adverse events
Measure
Moderate or Severe Psoriasis
n=52 participants at risk
Participants with moderate or severe psoriasis in treatment with Adalimumab
General disorders
Influenza like illness
9.6%
5/52 • Adverse events were collected from signing of informed consent until 70 days or 5 half-lives of drug

Additional Information

Global Medical Services

AbbVie (prior sponsor, Abbott)

Phone: 800-633-9110

Results disclosure agreements

  • Principal investigator is a sponsor employee AbbVie requests that any investigator or institution that plans on presenting/publishing results disclosure, provide written notification of their request 60 days prior to their presentation/publication. AbbVie requests that no presentation/publication will be instituted until 12 months after a study is completed, or after the first presentation/publication whichever occurs first. A delay may be proposed of a presentation/publication if AbbVie needs to secure patent or proprietary protection.
  • Publication restrictions are in place

Restriction type: OTHER