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Study identifier: NCT06932471 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Paroxysmal Nocturnal Hemoglobinuria  ·  Sponsor: Wuhan Createrna Science and Technology Co., Ltd

PhasePhase 3
Planned participants20
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Wuhan Createrna Science and Technology Co.,Ltd  ·  027-68788900  ·  lcyxzx@createrna.com

Always discuss trial participation with your own doctor first.

Locations (1)

Peking Union Medical College Hospital (PUMCH).Beijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06932471