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Long Term Safety Follow up of Haematopoietic Stem Cell Gene Therapy for the Wiskott Aldrich Syndrome

Study acronym: WASFUP
StatusActive, Not Recruiting
PhasePhase 1/2
SponsorGenethon
Started
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Record History

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  1. Notable Primary and study completion dates: Dec 2027 to Oct 2032
    • Trial status: Recruiting to Active, Not Recruiting
    • Secondary endpoints: details revised at 3 of 3 entries
    • Site details revised at 2 of 2 sites
    v7
  2. Minor Study title expanded, about 11 wordsv6
  3. Notable Primary and study completion dates: Dec 2019 to Dec 2027v5
  4. Minor 3 versions Re-verified since Oct 28, 2015, no change to tracked fieldsv2-v4
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
9 trials monitored
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An open follow up study of patients enrolled in the Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome and treated with autologous CD34+ cells transduced with the w1.6\_hWASP\_WPRE (VSVg) lentiviral vector.
Trial Details
NCT Number NCT02333760
Lead Sponsor Genethon
Conditions
(from sponsor)
Wiskott-Aldrich Syndrome
Related terms Wiskott-Aldrich Syndrome
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov