Contact SCGE




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
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