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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
EDIT-301 for Autologous Hematopoietic Stem Cell Transplant (HSCT) in Participants With Transfusion-Dependent Beta Thalassemia (TDT)
NCTID
NCT05444894
(View at clinicaltrials.gov)
Description
The purpose of this study is to evaluate the safety, tolerability, and efficacy of treatment with EDIT-301 in adult participants with Transfusion Dependent beta Thalassemia
(Show More)
Indication
Beta-Thalassemia, transfusion-dependent
Compound Name
Renizgamglogene autogedtemcel (EDIT-301)
Sponsor
Editas Medicine, Inc.
Funder Type
Industry
Status
Recruiting
Enrollment Count
9
Therapy Information
Target Gene/Variant
HBG1/HBG2
Therapy Type
Gene editing
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
ASCas12a mRNA
Dose 1
Min: 5.7 x 10^6 CD34+ cells/kg
Dose 2
Max: 11.9 x 10^6 CD34+ cells/kg
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase1, Phase2
Submit Date
2022-06-27
Completion Date
2025-12
Last Update
2024-01-29
Participation Criteria
Eligible Age
18 Years - 35 Years
Standard Ages
Adult
Eligible Sex
ALL
Locations
No.of Trial Sites
8
Locations
Canada,United States
Regulatory Information
Has US IND
True
Recent Updates
RMAT designation in 2023
Resources/Links
Patents
WO2017160890A1
Clinical Publications
https://ir.editasmedicine.com/static-files/dc33c7c9-a186-4136-ac7b-0de29a36a940
News and Press Releases
https://ir.editasmedicine.com/news-releases/news-release-details/editas-medicine-present-clinical-data-ruby-and-edithal-trials-0