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Clinical Trial Summary

This is a prospective, single-arm, open-label study. Twenty adult patients with transfusion-dependent β -thalassemia will be enrolled to receive Luspatercept with optimal supportive care, including blood transfusion and iron removal, based on the clinician's judgment and practice. The main objective of this study was to evaluate the efficacy and safety of Luspatercept in the treatment of adult patients with transfusion-dependent β -thalassaemia in Chinese clinical practice, and to provide evidence reference for subsequent clinical use.


Clinical Trial Description

Twenty adult patients with transfusion-dependent β -thalassemia will be enrolled to receive Luspatercept with optimal supportive care, being injected subcutaneously every 3 weeks ,by the dose of 1-1.25 mg/kg. The main objective of this study was to evaluate the efficacy and safety of Luspatercept in the treatment of adult patients with transfusion-dependent β -thalassaemia in Chinese clinical practice, and to provide evidence reference for subsequent clinical use. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05462548
Study type Interventional
Source Sun Yat-sen University
Contact Jianpei Fang, MD
Phone 008613682290830
Email jpfang2005@163.com
Status Recruiting
Phase Phase 4
Start date July 2022
Completion date April 30, 2023

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