drugset / Trial / NCT07816237

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

NCT07816237 ↗

Phase 3 Not yet recruiting 70 enrolled Bisirna Therapeutics (Suzhou) Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

A study of the efficacy and safety of VSA012 Injection compared to eculizumab for 24 weeks in patients with PNH.

Timeline

Start
2026-10-29
Primary completion
2027-09-30
Completion
2029-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Eculizumab Monoclonal antibody — —
Subject VSA012 Unknown — —