EUCTR2018-002935-88-DEActive, not recruitingPhase 1
A Long-term Follow-up Study of Subjects With ß-thalassemia or Sickle Cell Disease Treated with Autologous CRISPR-Cas9 Modified Hematopoietic Stem Cells (CTX001)
Vertex Pharmaceuticals Incorporated0 sites160 target enrollmentStarted: September 11, 2018Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Enrollment
- 160
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •1. Subjects (or his or her legally appointed and authorized
- •representative or guardian) must sign and date informed consent form
- •(ICF) and, where applicable, an assent form.
- •2. Subjects must have received CTX001 infusion in a parent study.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 34
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 80
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •1. There are no exclusion criteria.
Investigators
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