drugset / Trial / NCT03682536

A Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) Versus Epoetin Alfa for the Treatment of Anemia Due to IPSS-R Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) Participants Who Require Red Blood Cell Transfusions and Are ESA Naïve

NCT03682536 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the effectiveness of luspatercept (ACE-536) compared to epoetin alfa on red blood cell (RBC) transfusion independence (for at least 12 weeks) with a concurrent hemoglobin increase of at least 1.5 g/dL in participants with anemia due to revised international prognostic scoring system (IPSS-R) very low, low, or intermediate risk myelodysplastic syndromes (MDS) who require RBC transfusions and have never been exposed to erythropoiesis stimulating agent (ESA).

Timeline

Start
2019-01-02
Primary completion
2023-03-31
Completion
2027-09-28

Outcome

Met primary endpoint

registry analysis (superiority test); Luspatercept vs Epoetin Alfa; p <.0001; Odds Ratio (OR) 3.1 (95% CI 2.0 to 4.8) NCT03682536 ↗

paper reached the primary endpoint (110 [60%] vs 63 [35%]; common risk difference on response rate 25·4% [95% CI 15·8-35·0]; p<0·0001). PMID 39038479 ↗

release “the COMMANDS study, a Phase 3, open-label, randomized trial evaluating Reblozyl ® (luspatercept-aamt), met its primary endpoint” bms.com ↗

release “60.4% (n=110) of patients receiving Reblozyl vs. 34.8% (n=63) of patients receiving epoetin alfa achieved the primary endpoint” bms.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Luspatercept Protein / enzyme biologic 1.75 mg/kg Subcutaneous
Comparator epoetin alfa Protein / enzyme biologic 1050 iu/kg Subcutaneous