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Comparison · NCT04908189-612c55d3

Deucravacitinib vs Placebo: Number of Participants Meeting Psoriasis Area and Severity Index 75 (PASI 75) at Week 16

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Deucravacitinib vs Placebo: Number of Participants Meeting Psoriasis Area and Severity Index 75 (PASI 75) at Week 16. Trial comparisons, record NCT04908189-612c55d3. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04908189-612c55d3

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.4090.3350.488wilson
Risk in group 20.1540.1050.221wilson
Risk difference, group 1 minus group 20.2550.1550.348newcombe hybrid score
Risk ratio, group 1 over group 22.651.744.04log
Odds ratio, group 1 over group 23.792.196.56log
Number needed to treat, for one more participant with the outcome on Deucravacitinib than on Placebo3.932.886.46from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DeucravacitinibDeucravacitinib 6 mg daily63154OG000
Group 2PlaceboPlacebo daily23149OG001

Outcome

Type
SECONDARY
Title
Number of Participants Meeting Psoriasis Area and Severity Index 75 (PASI 75) at Week 16
Description
PASI is a measure of the average erythema, induration thickness, and scaling of psoriatic skin lesions (each graded on a 0 to 4 scale), weighted by the area of involvement (head, arms, trunk to groin, and legs to top of buttocks). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. PASI 75 is the number of participants who experience at least a 75% improvement in PASI score as compared with the baseline value. Baseline is defined as the last measurement on or prior to date/time of first dose of study treatment.
Time frame
Week 16
Population
All randomized participants of deucravacitinib and placebo with at least 3% body surface area (BSA) and at least static physician's global assessment (sPGA) 2 at baseline as pre-specified in protocol

Source ClinicalTrials.gov

Trial

Title
A Study to Determine the Efficacy and Safety of Deucravacitinib Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Are Naïve to Biologic Disease Modifying Anti-rheumatic Drugs or Had Previously Received TNFα Inhibitor Treatment
NCT number
NCT04908189
Phases
PHASE3
Conditions
Psoriatic Arthritis
Interventions
Deucravacitinib, Placebo, Apremilast
Lead sponsor
Bristol-Myers Squibb
Results first posted
2025-04-13

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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