Study of Safety & PK of Luspatercept (ACE-536) in Pediatric Participants Who Require Regular RBC Transfusions Due to Beta (β)-Thalassemia.
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT04143724 |
Recruitment Status :
Recruiting
First Posted : October 29, 2019
Last Update Posted : February 13, 2023
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Sponsor:
Celgene
Collaborator:
Acceleron Pharma Inc. (a wholly owned subsidiary of Merck Sharp and Dohme, a subsidiary of Merck & Co., Inc.)
Information provided by (Responsible Party):
Celgene
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No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : | Recruiting |
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Estimated Primary Completion Date : | June 30, 2026 |
Estimated Study Completion Date : | November 17, 2026 |