drugset / Trial / NCT06045689

A Study to Assess Luspatercept in Lower-risk Myelodysplastic Syndrome Participants

NCT06045689

Phase 3 Active not recruiting 106 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of Luspatercept when administered at the maximum approved dose in low-risk Myelodysplastic Syndrome participants who require red blood cell transfusions.

Timeline

Start
2023-10-05
Primary completion
2025-10-01
Completion
2027-09-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Luspatercept Protein / enzyme biologic