Clinical Trial

Study of Safety and Efficacy of MY008211A in in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

Not Yet Recruiting Phase 2
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Summary
The main purpose of this study is to evaluate the efficacy of MY008211A in adult patients with PNH, showing signs of active hemolysis.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2023-11-10; most recent amendment 2025-07-27.
Trial Details
NCT Number NCT06134414
Lead Sponsor Wuhan Createrna Science and Technology Co., Ltd
Conditions Paroxysmal Nocturnal Hemoglobinuria (PNH)
Enrollment 40 participants
Start Date 2025-12
Primary Completion 2027-07 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2025-07-29