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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
A Study Evaluating the Safety and Efficacy of the GMCN-508A Drug Product in Transfusion-dependent α-Thalassemia Participants
NCTID
NCT05757245
(View at clinicaltrials.gov)
Description
This is a non-randomized, open label, single-site, single-dose, phase 1 study in up to 5 participants (between 5 and 35 years of age, inclusive) with Transfusion-dependent α-thalassemia. The study will evaluate the safety and efficacy of autologous hematopoietic stem cell transplantation (HSCT) using GMCN-508A Drug Product \[autologous CD34+ hematopoietic stem cells transduced with GMCN-508A lentiviral vector encoding the human α-globin gene\].
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Development Status
Active
Indication
Transfusion-dependent Alpha-Thalassemia
Disease Ontology Term
DOID:1099
Compound Name
GMCN-508A
Sponsor
First Affiliated Hospital of Guangxi Medical University
Funder Type
Other
Recruitment Status
Recruiting
(Click here for study contact information)
Enrollment Count
5
Results Posted
Not Available
Therapy Information
Target Gene/Variant
HBA
Therapy Type
Gene transfer
Therapy Route
Ex-vivo
Mechanism of Action
Functional gene replacement
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
Submit Date
2023-02-24
Completion Date
2030-12-31
Last Update
2023-04-18
Participation Criteria
Eligible Age
5 Years - 35 Years
Standard Ages
Child, 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.