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RECRUITING
NCT06932744
PHASE3

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

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 compared to eculizumab in PNH patients.

Official title: A Randomized, Multicenter, Active-comparator Controlled, Open-label Trial to Evaluate Efficacy and Safety of MY008211A Tablets in PNH Patients Who Are Naive to Complement Inhibitor Therapy

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2024-08-30

Completion Date

2025-12-30

Last Updated

2025-05-09

Healthy Volunteers

No

Interventions

DRUG

MY008211A tablets

Participants will receive MY008211A at a dose of 400 mg orally b.i.d for 24 weeks

DRUG

Eculizumab Injection

Eculizumab Injection for 24 weeks

Locations (2)

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Chinese Academy of Medical Sciences Hematology Hospital

Tianjin, Tianjin Municipality, China