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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
Investigation Into the Use of BAH243 Lentiviral Vector for Gene Therapy in Treating Sickle Cell Disease
NCTID
NCT06399107
(View at clinicaltrials.gov)
Description
This study is an open-label, non-randomized, single-dose Phase 1/2 trial involving around 85 adult and pediatric participants aged between 2 and 50 years with sickle cell disease (SCD). It aims to assess the effectiveness of hematopoietic stem cell transplantation (HSCT) using BAH243 for SCD.
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Development Status
Active
Indication
Sickle Cell Disease, Sickle-Cell Disease With Crisis
Disease Ontology Term
DOID:0081445
Compound Name
BAH243
Sponsor
Essen Biotech
Funder Type
Other
Recruitment Status
Recruiting
Enrollment Count
85
Results Posted
Not Available
Therapy Information
Target Gene/Variant
HBB
Therapy Type
Gene transfer
Therapy Route
Ex-vivo
Mechanism of Action
Overexpression of protective allele/gene
Route of Administration
Intravenous
Drug Product Type
Autologous cells
Target Tissue/Cell
CD34+ cells
Delivery System
Viral transduction
Vector Type
LV
Editor Type
none
Dose 1
Transduced CD34+ cells
Dose 2
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase1, Phase2
Submit Date
2024-04-29
Completion Date
2025-12-28
Last Update
2024-11-05
Participation Criteria
Eligible Age
2 Years - 90 Years
Standard Ages
Child, Adult, Older adult
Sexes Eligible for Study
ALL
Locations
No.of Trial Sites
1
Locations
China
Regulatory Information
Has US IND
False
FDA Designations
Recent Updates
Resources/Links
Resources/Links
No External Links Available.