Clinical trial

A Study of Luspatercept (ACE-536) to Treat Anemia Due to Very Low, Low, or…

NCT02631070 · Celgene, Industry · Completed

Key facts

NCT number NCT02631070
Title A Study of Luspatercept (ACE-536) to Treat Anemia Due to Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes
Official title A Phase 3, Double-blind, Randomized Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) Versus Placebo for the Treatment of Anemia Due to the IPSS-R Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes in Subjects With Ring Sideroblasts Who Require Red Blood Cell…
Acronym MEDALIST
Lead sponsor Celgene, Industry
Collaborators Acceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway, NJ USA Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Myelodysplastic Syndromes
Intervention type Drug, Other
Interventions Luspatercept, Placebo
Enrollment 229
Start date Feb 9, 2016
Primary completion Jun 18, 2019
Completion Nov 26, 2020
First posted Dec 15, 2015
Last update posted Dec 17, 2021
Countries Belgium, Canada, France, Germany, Italy, Netherlands, Spain, Sweden, Turkey (Türkiye), United Kingdom, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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