Condition: Psoriasis (PsO) · Sponsor: Bristol-Myers Squibb
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.
This description comes directly from the study's public registry record.
BMS Study Connect Contact Center www.BMSStudyConnect.com · 855-907-3286 · Clinical.Trials@bms.com
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| University of California San Diego | La Jolla, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07017699