Status: Recruiting
A Clinical Study to Assess Sutacimig in Participants With Congenital Factor VII Deficiency
Open-label study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of a single dose of sutacimig monotherapy in participants with congenital FVII deficiency (FVIID).
Participants needed: 18
Trial details
Phase: Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Hemab ApSUpdated: May 29, 2026Locations: 1
Eligibility criteria
Age 18 to 60 years, inclusive, at the time of signing informed consent. [+3]
Presence of known inhibitors to FVII or FVIIa [+6]