Active, not recruitingPhase 3NCT04908189

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

Studying NON RARE IN EUROPE: Psoriatic arthritis

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Key facts

Sponsor
Bristol-Myers Squibb
Principal Investigator
Bristol-Myers Squibb
Bristol-Myers Squibb
Intervention
Deucravacitinib(drug)
Enrollment
729 target
Eligibility
18 years · All sexes
Timeline
20212026

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT04908189 on ClinicalTrials.gov

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