Study of Safety and Efficacy of MY008211A in Patients With Residual Anemia Despite Anti-C5 Antibody Treatment

Recruiting now · Phase 3

Conditions studied: Paroxysmal Nocturnal Hemoglobinuria

In brief

The main purpose of this study is to evaluate the efficacy of MY008211A in PNH patients with residual anemia despite treatment with anti-C5 antibody.

Key facts

Study ID
NCT06932471
Run by
Wuhan Createrna Science and Technology Co., Ltd
People needed
20
Starts
2024-08-30
Expected to finish
2025-12-30
Last updated by the study team
2025-05-09

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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