A Phase 3 Study to Evaluate the Safety and Efficacy of a Single Dose of CTX001 in Pediatric Subjects With Transfusion-Dependent β-Thalassemia

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This is a single-dose, open-label study in pediatric participants with TDT. The study will evaluate the safety and efficacy of autologous CRISPR-Cas9 modified CD34+ human hematopoietic stem and progenitor cells (hHSPCs) (CTX001).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 11
Healthy Volunteers: f
View:

• Diagnosis of TDT as defined by:

‣ Documented homozygous or compound heterozygous β-thalassemia including β-thalassemia/hemoglobin E (HbE). Participants can be enrolled based on historical data, but a confirmation of the genotype using the study central laboratory will be required before busulfan conditioning

⁃ History of at least 100 mL/kilograms (kg)/year of packed RBC transfusions in the prior 24 months before signing of consent (or the last rescreening for patients going through repeat screening) or, for participants initiating transfusion therapy \<24 months before signing of consent, requirement for packed RBC transfusion at least every 3 to 4 weeks for ≥6 months

• Eligible for autologous stem cell transplant as per investigator's judgment.

Locations
United States
Tennessee
TriStar Medical Group Children's Specialists - Pediatric Oncology
RECRUITING
Nashville
Other Locations
Canada
Hospital for Sick Children - Hematology
RECRUITING
Toronto
Germany
University Hospital Dusseldorf - Department of Pediatric Oncology, Hematology and Clinical Immunology
RECRUITING
Düsseldorf
Italy
IRCSS Ospedale Pediatrico Bambino Gesu - Dipartimento di Onco-Ematologia e Terapia Cellulare e Genica
RECRUITING
Rome
United Kingdom
Great Ormond Street Hospital for Children
RECRUITING
London
St.Mary's Hospital - Children's Clinical Research Facility
RECRUITING
London
Contact Information
Primary
Medical Information
medicalinfo@vrtx.com
617-341-6777
Time Frame
Start Date: 2022-05-03
Estimated Completion Date: 2026-05-31
Participants
Target number of participants: 15
Treatments
Experimental: CTX001
CTX001 (autologous CD34+ hHSPCs modified with CRISPR-Cas9 at the erythroid lineage-specific enhancer of the BCL11A gene). Participants will receive single infusion of CTX001 through central venous catheter.
Sponsors
Leads: Vertex Pharmaceuticals Incorporated
Collaborators: CRISPR Therapeutics

This content was sourced from clinicaltrials.gov