Clinical Trial

Study of Safety and Efficacy of HS-10542 in Patients With Paroxysmal Nocturnal Hemoglobinuria

Recruiting Phase 1/2
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Summary
This was a phase 1b/2,open label, multi-center study to assess efficacy and safety of HS-10542 in adulte patients with paroxysmal nocturnal hemoglobinuria (PNH) with signs of active hemolysis.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-03-10.
Trial Details
NCT Number NCT07470762
Lead Sponsor Jiangsu Hansoh Pharmaceutical Co., Ltd.
Conditions Paroxysmal Nocturnal Hemoglobinuria
Enrollment 50 participants
Start Date 2026-02-14
Primary Completion 2027-05-30 (estimated)
Study Completion 2029-07-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-13