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Evaluation of Safety and Efficacy of CTX001 in Pediatric Participants With Severe Sickle Cell Disease (SCD)

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NCT05329649 · readout in 291 d

Sponsored by Vertex Pharmaceuticals Incorporated (industry) · VRTX — their whole pipeline →. With CRISPR Therapeutics.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
13actual
Sites
7
Countries
Germany, Italy, United Kingdom +1

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-05-02actualWhen the study began enrolling
Primary completion2027-06-06estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-06-06estimatedThe whole study's end, after follow-up
First posted2022-04-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Sickle Cell Disease
  • Hydroxyurea Failure
  • Hydroxyurea Intolerance
  • Hemoglobinopathies
  • Hematological Diseases

Intervention

  • Biological: CTX001 — also filed as Exagamglogene autotemcel, Exa-cel

Primary outcome

what the primary-completion date above is the date OF
Proportion of Participants who do not Have any Severe Vaso-occlusive Crises (VOCs) for at Least 12 Consecutive Months (VF12)
measured Up to 24 Months After CTX001 Infusion

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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