Study Summary
This is a Phase 1/2, open label, safety, and efficacy study of the administration of LentiGlobin BB305 Drug Product to participants with either transfusion dependent beta-thalassemia (TDT) or sickle cell disease (SCD).
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Submit an InquiryInterventions
LentiGlobin BB305 Drug ProductDRUG
LentiGlobin BB305 Drug Product was administered by intravenous (IV) infusion.
Study Locations
| Facility | City | State | Country |
|---|---|---|---|
| N/A | Paris | France |