ConductScience.org, home

Comparison · NCT04908189-b4350f64

Deucravacitinib vs Placebo: Number of Participants Meeting American College of Rheumatology (ACR) 50 at Week 16

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

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

Download JSON
Cite this record

ConductScience Library. Deucravacitinib vs Placebo: Number of Participants Meeting American College of Rheumatology (ACR) 50 at Week 16. Trial comparisons, record NCT04908189-b4350f64. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04908189-b4350f64

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2880.2410.341wilson
Risk in group 20.1630.1270.209wilson
Risk difference, group 1 minus group 20.1250.05950.189newcombe hybrid score
Risk ratio, group 1 over group 21.761.32.4log
Odds ratio, group 1 over group 22.071.413.06log
Number needed to treat, for one more participant with the outcome on Deucravacitinib than on Placebo85.2816.8from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DeucravacitinibDeucravacitinib 6 mg daily90312OG000
Group 2PlaceboPlacebo daily51312OG001

Outcome

Type
SECONDARY
Title
Number of Participants Meeting American College of Rheumatology (ACR) 50 at Week 16
Description
The American College of Rheumatology (ACR) 50 is defined as 50% improvement over baseline in tender (68) and swollen (66) joint counts and a 50% improvement in 3 of the 5 remaining core data set measures: Participant Global Assessment of Disease Activity; Participant Global Assessment of Pain; Participant assessment of physical function; Physician Global Assessment of psoriatic arthritis; and Acute phase reactant value of high sensitivity C-reactive protein (hsCRP). 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 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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT04908189-b4350f64