drugset / Trial / NCT05925504

The Tapering Dose of Luspatercept in Patients With Lower-risk Myelodysplastic Syndromes

NCT05925504

NaSingle-groupOpen-labelTreatment

Summary

This is a prospective, single center, single-arm, phase 2 study. The aim of this study is to evaluate the efficacy and safety of Luspatercept for Patients with Lower-risk Myelodysplastic Syndromes (MDS).

Timeline

Start
2023-07-01
Primary completion
2026-06-30
Completion
2026-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Luspatercept Protein / enzyme biologic 1.75 mg/kg Subcutaneous