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Trial · NCT02847598

Results by group758

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Part A: Change From Baseline in Active Joint Count (28-joint Assessment) to Week 24Part A: Placebo-12.7Standard Deviation 10.3joints
Part A: Change From Baseline in Active Joint Count (28-joint Assessment) to Week 24Part A: BIIB059 50 mg-9.0Standard Deviation 5.7joints
Part A: Change From Baseline in Active Joint Count (28-joint Assessment) to Week 24Part A: BIIB059 150 mg-13.0Standard Deviation NAjoints
Part A: Change From Baseline in Active Joint Count (28-joint Assessment) to Week 24Part A: BIIB059 450 mg-14.5Standard Deviation 8.7joints
Part B: Percent Change From Baseline in Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity (CLASI-A) Score to Week 16Part B: Placebo-15.03Standard Deviation 37.23percent change
Part B: Percent Change From Baseline in Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity (CLASI-A) Score to Week 16Part B: BIIB059 50 mg-35.52Standard Deviation 33.35percent change
Part B: Percent Change From Baseline in Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity (CLASI-A) Score to Week 16Part B: BIIB059 150 mg-47.11Standard Deviation 34.10percent change
Part B: Percent Change From Baseline in Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity (CLASI-A) Score to Week 16Part B: BIIB059 450 mg-41.66Standard Deviation 37.33percent change
Part A : Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 24Part A: Placebo42.11percentage of participants
Part A : Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 24Part A: BIIB059 50 mg50percentage of participants
Part A : Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 24Part A: BIIB059 150 mg16.67percentage of participants
Part A : Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 24Part A: BIIB059 450 mg64.10percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: PlaceboWeek 1212.12percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 50 mgWeek 1238.46percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 150 mgWeek 1248.00percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 450 mgWeek 1237.50percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: PlaceboWeek 1621.88percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 50 mgWeek 1638.46percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 150 mgWeek 1644.00percentage of participants
Part B: Percentage of Participants With Cutaneous Lupus Erythematosus Disease Area and Severity Index Activity- 50 (CLASI-50) Response at Week 12 and 16Part B: BIIB059 450 mgWeek 1646.51percentage of participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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