Clinical Trial

A Study to Assess Deucravacitinib Safety in Pregnancy

Recruiting
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Summary
The purpose of this study is to assess pregnancy and infant outcomes among pregnant participants enrolled in an established North American pregnancy registry (Organization of Teratology Information Specialists \[OTIS\]) who were exposed to deucravacitinib.
Trial Details
NCT Number NCT07017699
Lead Sponsor Bristol-Myers Squibb
Conditions Psoriasis (PsO)
Enrollment 900 participants
Start Date 2025-03-21
Primary Completion 2028-04-01 (estimated)
Study Completion 2029-02-28 (estimated)
Updated on ClinicalTrials.gov 2025-06-12