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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
A Safety and Efficacy Study Evaluating CS-101 in Subjects With β-Thalassemia Major
NCTID
NCT06291961
(View at clinicaltrials.gov)
Description
The goal of this open label, single-arm clinical study is to learn about the safety and efficacy of CS-101 in treating patients with β-thalassemia major anemia.
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Indication
Beta-Thalassemia Major
Compound Name
CS-101
Sponsor
CorrectSequence Therapeutics Co., Ltd
Funder Type
Industry
Status
Recruiting
Enrollment Count
8
Therapy Information
Target Gene/Variant
BCL11A
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
Electroporation
Vector Type
none
Editor Type
transformer BE RNP
Dose 1
Transduced CD34+ cells
Dose 2
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase1
Submit Date
2024-02-23
Completion Date
2025-07
Last Update
2024-07-01
Participation Criteria
Eligible Age
12 Years - 35 Years
Standard Ages
Child, Adult
Eligible Sex
ALL
Locations
No.of Trial Sites
3
Locations
China
Regulatory Information
Has US IND
False
Recent Updates
Resources/Links
Clinical Publications
(Poster) Rapid, Efficient and Durable Fetal Hemoglobin Production Following CS-101 Treatment in Transfusion-Dependent β-Thalassemia Participants: An Autologous, Ex Vivo Edited CD34+ Stem Cell Product Using the Innovative Transformer Base Editor (tBE) - ASH 2024
News and Press Releases
Locally-Developed Gene Editing Technology Cures Boy with Serious Blood Disorder
Preclinical Publications
Eliminating base-editor-induced genome-wide and transcriptome-wide off-target mutations
Base editing of the HBG promoter induces potent fetal hemoglobin expression with no detectable off-target mutations in human HSCs
Protocol
Protocol for examining and eliminating base editor-induced genome-wide and transcriptome-wide off-target mutations