A Phase 3b, Open-label Study Evaluating the Efficacy and Safety of Luspatercept (BMS-986346/ACE-536) Initiated at Maximum Approved Dose in LR-MDS with IPSS-R Very Low-, Low-, or Intermediate-risk Who Require RBC Transfusions (MAXILUS)

Protocol No

BMS-CA0561060

Phase

III

Summary

This project is being done to learn more about Luspatercept if administrated at the maximum approved starting dose to assess that a quicker benefit can be seen in your transfusion burden and hemoglobin level.

Description

Study of Luspatercept in lower-risk myelodysplastic syndrome participants

Participating Institutions

Froedtert Hospital

Status

OPEN TO ACCRUAL