Contact SCGE




Gene Therapy Trial Report

Summary

A Clinical Study to Evaluate the Use of a Cryopreserved Formulation of OTL-103 in Subjects With Wiskott-Aldrich Syndrome


NCTID NCT03837483 (View at clinicaltrials.gov)
Description
Development Status Approved
Indication Wiskott-Aldrich Syndrome
Disease Ontology Term DOID:9169
Compound Name WASKYRA
Compound Alias Etuvetidigene autotemcel , TLT003, OTL-103
Compound Description pCCLsin.cPPT.hw1.6.hWAS.WPREmut
Sponsor Fondazione Telethon
Funder Type Other
Recruitment Status
Active not recruiting
Enrollment Count 10 (ACTUAL)
Results Posted Not Available

Therapy Information


Target Gene/Variant WAS
Therapy Type Gene transfer
Therapy Route Ex-vivo
Mechanism of Action Functional gene replacement
Route of Administration Intravenous
Drug Product Type Autologous cells
Target Tissue/Cell CD34+ cells
Delivery System Viral transduction
Vector Type LV
Editor Type none
Dose 1 Transduced CD34+ cells (Range: 2 - 15E6 cells/kg; Median: 7.05E6 cells/kg)
Dose 2 Minimum recommended dose: 7E6 CD34+ cells/kg

Study Record Dates


Current Stage Phase3
Submit Date 2019-02-08
Completion Date 2027-09
Last Update 2025-09-29

Participation Criteria


Eligible Age <=65 Years
Standard Ages Child, Adult, Older adult
Sexes Eligible for Study ALL
Eligibility Criteria
Inclusion Criteria: * Age: up to 65 years * Diagnosis of WAS defined by genetic mutation and at least one of the following criteria: * Severe Wiskott-Aldrich Syndrome (WAS) gene mutation, defined by literature data (genotype/phenotype studies).; * Absent WASP expression, assessed by flow cytometry; * Severe clinical score (Zhu clinical score ≥ 3); * No human leukocyte antigen (HLA)-identical related donor available for hematopoietic stem cells transplant (HSCT). Exclusion Criteria: * End-organ dysfunction, severe active infection not responsive to treatment or other severe disease or clinical condition which, in the judgment of the investigator, would make the patient inappropriate for entry into this study. * Malignant neoplasia (except local skin cancer) or a documented history of hereditary cancer syndrome. * Myelodysplasia, cytogenetic alterations characteristic of myelodysplastic syndrome and acute myeloid leukaemia , or other serious haematological disorders * Documented human immunodeficiency virus (HIV) infection * Prior allogeneic hematopoietic stem cell transplantation, with evidence of residual cells of donor origin * Symptomatic herpes zoster, not responsive to specific treatment * Evidence of acute tuberculosis * Acute or chronic stable Hepatitis B * Presence of positive Hepatitis C RNA test result at screening * Patients not eligible for mobilization protocols in order to obtain CD34+ cells * Previous Gene Therapy
View Inclusion and Exclusion Criteria at ClinicalTrials.gov

Locations


No.of Trial Sites 2
Locations United States,Italy

Regulatory Information


Has US IND True
FDA Designations Orphan Drug Designation, Rare Pediatric Disease Designation, Regenerative Medicine Advanced Therapy
Recent Updates FDA approved 12/9/25

Resources/Links