drugset / Trial / NCT06164821

Clinical Observation of Luspatercept in Treatment of Chinese Adult β-thalassaemia Patients With TD β-thalassemia

NCT06164821

NaSingle-groupOpen-labelTreatment

Summary

To assesse the efficacy and safety of luspatercept versus placebo in China patients with transfusion-dependent β-thalassaemia.

Timeline

Start
2024-01-01
Primary completion
2024-01-01
Completion
2024-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Luspatercept Protein / enzyme biologic 1.25 mg/kg Subcutaneous

Indications

No indication recorded.