CompletedPHASE1, PHASE2NCT02151526
A Study Evaluating the Safety and Efficacy of LentiGlobin BB305 Drug Product in β-Thalassemia Major (Also Referred to as Transfusion-dependent β-Thalassemia [TDT]) and Sickle Cell Disease
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
- Genetix Biotherapeutics Inc.
- Principal Investigator
- Jean-Antoine Ribeil, MD, MDbluebird bio, Inc.
- Intervention
- LentiGlobin BB305 Drug Product(drug)
- Enrollment
- 7 enrolled
- Eligibility
- 5-35 years · All sexes
- Timeline
- 2013 – 2019
Study locations (1)
- Paris, France
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.
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