A Clinical Study to Evaluate the Use of a Cryopreserved Formulation of OTL-103 in Subjects With Wiskott-Aldrich Syndrome
Condition(s) studied
Investigational drug(s) / intervention(s)
OTL-103: Autologous hematopoietic stem cells collected from mobilized peripheral blood transduced ex vivo with a lentiviral vector encoding the WAS cDNA
Study summary
This is an open-label, single arm study to evaluate the cryopreserved formulation of OTL-103 Gene Therapy. OTL-103 consists of autologous CD34+ hematopoietic stem cells in which the gene encoding for the Wiskott-Aldrich Syndrome is introduced by means of a third generation lentiviral vector.
Eligibility
Primary outcome measure(s)
- Annualized rate of severe infections from 6 to 18 months after gene therapy compared with 1 year before gene therapy — 18 months
- Annualized rate of moderate and severe bleeding episodes up to 1 year after gene therapy compared with 1 year before gene therapy — 12 months
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Children's Healthcare of Atlanta, Inc | Atlanta | Georgia | |
| Ospedale San Raffaele - Telethon Institute for Gene Therapy (OSR-TIGET) | Milan | Italy |
More Fondazione Telethon trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03837483 on ClinicalTrials.gov ↗ ← All trials in Italy