Geneva, Sept. 21 -- International Clinical Trials Registry received information related to the study (NCT07816237) titled 'A Multicenter, Randomized, Open-Label, Positive Controlled Phase III Study to Evaluate the Efficacy and Safety of VSA012 Injection in Participants With Paroxysmal Nocturnal Hemoglobinuria Who Are Naive to Complement Inhibitor Therapy' on Sept. 4.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Bisirna Therapeutics (Suzhou) Co., Ltd.
Condition:
Paroxysmal Nocturnal Hemoglobinuria, PNH
Intervention:
Drug: VSA012
Recruitment Status: Not recruiting
Phase: Phase 3
Date of First Enr...