Geneva, April 20 -- International Clinical Trials Registry received information related to the study (ChiCTR2600122157) titled 'Clinical Study on the Efficacy and Safety of Luspatercept in Combination with Thalidomide for Adult Patients with ß-Thalassaemia' on April 9.

Study Type: Interventional study

Study Design: Single arm

Primary Sponsor: The 923rd Hospital of the Joint Logistics Support Force of the People's Liberation Army

Condition: ß-Thalassaemia

Intervention: Luspatercept + Thalidomide Group:Luspatercept: 1.0 mg/kg, subcutaneous (SC) administration, every 21 days

Recruitment Status: Recruiting

Phase: N/A

Date of First Enrollment: 2026-02-01

Target Sample Size: Luspatercept + Thalidomide Group:30;

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