Last updated on August 2018

A Study Evaluating the Efficacy and Safety of the LentiGlobin BB305 Drug Product in Subjects With Transfusion-Dependent -Thalassemia Who do Not Have a 0/ 0 Genotype


Brief description of study

This is a single-arm, multi-site, single-dose, Phase 3 study in approximately 23 subjects 50 years of age with transfusion-dependent -thalassemia (TDT), also known as -thalassemia major, who do not have a 0 mutation at both alleles of the hemoglobin (HBB) gene. The study will evaluate the efficacy and safety of autologous hematopoietic stem cell transplantation (HSCT) using LentiGlobin BB305 Drug Product.

Clinical Study Identifier: NCT02906202

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Oakland, CA United States
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Chicago, IL United States
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Philadelphia, PA United States
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Marseille, France
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Hannover, Germany
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Thessaloniki, Greece
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Bangkok, Thailand
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London, United Kingdom
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Recruitment Status: Open


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