RecruitingPhase 3NCT06932744

Study of Safety and Efficacy of MY008211A in Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients Who Are Naive to Complement Inhibitor Therapy

Studying Paroxysmal nocturnal hemoglobinuria

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Key facts

Sponsor
Wuhan Createrna Science and Technology Co., Ltd
Intervention
MY008211A tablets(drug)
Enrollment
66 enrolled
Eligibility
18-75 years · All sexes
Timeline
20242025

Study locations (2)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06932744 on ClinicalTrials.gov

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