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RECRUITING
NCT06932471
PHASE3

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

Sponsor: Wuhan Createrna Science and Technology Co., Ltd

View on ClinicalTrials.gov

Summary

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.

Official title: A Multicenter, Single-arm, Open-label Phase III Study to Evaluate Efficacy and Safety of MY008211A Tablets in Patients With PNH and Residual Anemia, Despite Treatment With Anti-C5 Antibody.

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2024-08-30

Completion Date

2025-12-30

Last Updated

2025-05-09

Healthy Volunteers

No

Interventions

DRUG

MY008211A tablets

MY008211A tablets Participants will receive MY008211A at a dose of 400 mg orally b.i.d

Locations (1)

Peking Union Medical College Hospital (PUMCH).

Beijing, Beijing Municipality, China