drugset / Trial / NCT03655678

A Safety and Efficacy Study Evaluating CTX001 in Participants With Transfusion-Dependent β-Thalassemia

NCT03655678 ↗

NaSingle-groupOpen-labelTreatment

Summary

This is a single-arm, open-label, multi-site, single-dose Phase 1/2/3 study in participans with transfusion-dependent β-thalassemia (TDT). The study will evaluate the safety and efficacy of autologous CRISPR-Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (hHSPCs) using CTX001.

Timeline

Start
2018-09-14
Primary completion
2025-11-13
Completion
2025-11-13

Outcome

Met primary endpoint

paper transfusion independence occurred in 32 (91%; 95% confidence interval, 77 to 98; P<0.001 against the null hypothesis of a 50% response). PMID 38657265 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject EXAGAMGLOGENE AUTOTEMCEL CRISPR / gene editing — Intravenous

Indications