drugset / Trial / NCT06933914

Long-term Safety and Tolerability of MY008211A Tablets in Patients With Paroxysmal Nocturnal Hemoglobinuria

NCT06933914

Phase 2/3 Recruiting 120 enrolled Wuhan Createrna Science and Technology Co., Ltd
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, single-arm, open-label study to characterize long-term safety and tolerability of MY008211A tablets and to provide access to MY008211A tablets to patients with PNH who have completed Phase 2 or 3 studies with MY008211A tablets.

Timeline

Start
2024-11-30
Primary completion
2026-12-30
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject MY008211A Unknown 400 mg Oral