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RECRUITING

Study of Ultomiris® (Ravulizumab) Safety in Pregnancy

NCT06312644

The primary objective of this study is to describe the frequency and characteristics of pregnancy outcomes and maternal complications among participants exposed to Ultomiris and to describe the frequency and characteristics of selected fetal/neonatal/infant outcomes in utero, at birth, and through 1 year of age after exposure in utero or via breastmilk.

Ultomiris-exposed Pregnant/ PostpartumPregnancyParoxysmal Nocturnal Hemoglobinuria (PNH)+3 more

Alexion Pharmaceuticals, Inc.75 participantsStarted Dec 2024

Boston, Massachusetts, United States • Melbourne, Victoria, Australia • Paris, France +4 more locations

Data from ClinicalTrials.govTerms