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NOT YET RECRUITING
NCT06134414
PHASE2

Study of Safety and Efficacy of MY008211A in in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

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 adult patients with PNH, showing signs of active hemolysis.

Official title: A Multi-center, Randomized, Parallel, Open-label Clinical Phase II Study, to Evaluate the Efficacy and Safety of MY008211A in Adult Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients With Signs of Active Hemolysis

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2025-12

Completion Date

2027-12

Last Updated

2025-07-29

Healthy Volunteers

No

Interventions

DRUG

MY008211A tablets

dose 1 (400 mg BID) and dose 2 (600 mg BID) in a 1:1 ratio by central randomization