CompletedPhase 2NCT03342404
A Study to Determine the Efficacy and Safety of Luspatercept in Adults With Non Transfusion Dependent Beta (β)-Thalassemia
Studying Beta-thalassemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celgene
- Principal Investigator
- Jeevan Shetty, MDCelgene Corporation
- Intervention
- Luspatercept(drug)
- Enrollment
- 145 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2018 – 2022
Study locations (16)
- Children's Hospital of Los Angeles, Los Angeles, California, United States
- Local Institution - 501, Los Angeles, California, United States
- Children's Hospital and Research Center at Oakland, Oakland, California, United States
- Local Institution - 503, Chicago, Illinois, United States
- Local Institution - 102, Athens, Greece
- Local Institution - 101, Athens, Greece
- Local Institution - 205, Cagliari, Italy
- Universita degli Studi di Cagliari - ASL8, Cagliari, Italy
- Local Institution - 202, Genoa, Italy
- Local Institution - 201, Milan, Italy
- Local Institution - 203, Naples, Italy
- Local Institution - 206, Naples, Italy
- Local Institution - 204, Orbassano, Italy
- Local Institution - 301, Hazmiyeh, Lebanon
- Local Institution - 401, Bangkok, Thailand
- +1 more locations on ClinicalTrials.gov
Collaborators
Acceleron Pharma, Inc., a wholly-owned subsidiary of Merck & Co., Inc., Rahway, NJ USA
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT03342404 on ClinicalTrials.govOther trials for Beta-thalassemia
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