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Trial · NCT04908189

Results by group262

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Meeting American College of Rheumatology (ACR) 20 at Week 16Deucravacitinib169Participants
Number of Participants Meeting American College of Rheumatology (ACR) 20 at Week 16Placebo123Participants
Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) at Week 16Deucravacitinib-1.3133Standard Deviation 1.17420score on a scale
Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) at Week 16Placebo-0.9095Standard Deviation 1.10470score on a scale
Change From Baseline in Health Assessment Quiestionnaire - Disability Index (HAQ-DI) at Week 16Deucravacitinib-0.3103Standard Deviation 0.46159score on a scale
Change From Baseline in Health Assessment Quiestionnaire - Disability Index (HAQ-DI) at Week 16Placebo-0.2219Standard Deviation 0.46858score on a scale
Number of Participants Meeting Psoriasis Area and Severity Index 75 (PASI 75) at Week 16Deucravacitinib63Participants
Number of Participants Meeting Psoriasis Area and Severity Index 75 (PASI 75) at Week 16Placebo23Participants
Change From Baseline in the 36-item Short Form (SF-36) Physical Component Summary (PCS) Score at Week 16Deucravacitinib6.194Standard Deviation 7.4640Score on a scale
Change From Baseline in the 36-item Short Form (SF-36) Physical Component Summary (PCS) Score at Week 16Placebo4.262Standard Deviation 7.0328Score on a scale
Number of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) at Week 16Deucravacitinib74Participants
Number of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) at Week 16Placebo66Participants
Number of Participants Meeting Achievement of Minimal Disease Activity (MDA) at Week 16Deucravacitinib80Participants
Number of Participants Meeting Achievement of Minimal Disease Activity (MDA) at Week 16Placebo46Participants
Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score at Week 16Deucravacitinib2.6Standard Deviation 8.17Score on a scale
Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score at Week 16Placebo1.9Standard Deviation 8.54Score on a scale
Number of Participants Meeting Dactylitis Resolution at Week 16Deucravacitinib43Participants
Number of Participants Meeting Dactylitis Resolution at Week 16Placebo36Participants
Number of Participants Meeting American College of Rheumatology (ACR) 50 at Week 16Deucravacitinib90Participants
Number of Participants Meeting American College of Rheumatology (ACR) 50 at Week 16Placebo51Participants

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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