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Gene Therapy Trial Browser
Clinical Trial Report
Gene Therapy Trial Report
Summary
A Study to Investigate the Efficacy and Safety of OTL-203 in Subjects with MPS-IH Compared with Standard of Care with Allogeneic HSCT
NCTID
NCT06149403
(View at clinicaltrials.gov)
Description
A multi-center randomized clinical trial to compare OTL-203 (gene therapy) with stem cell transplant (standard of care) in patients with MPS-IH (Hurler syndrome).
(Show More)
Development Status
Active
Indication
Mucopolysaccharidosis Type I (Hurler Syndrome)
Disease Ontology Term
DOID:12802
Compound Name
OTL-203
Compound Description
Autologous CD34+ cells transduced with IDUA lentiviral vector
Sponsor
Orchard Therapeutics
Funder Type
Industry
Recruitment Status
Active not recruiting
Enrollment Count
41
Results Posted
Not Available
Therapy Information
Target Gene/Variant
IDUA
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
Mean dose: 20.9E6 transduced CD34+ cells/kg
Dose 2
Dose 3
Dose 4
Dose 5
Study Record Dates
Current Stage
Phase3
Submit Date
2023-11-17
Completion Date
2031-03
Last Update
2025-03-27
Participation Criteria
Eligible Age
28 Days - 30 Months
Standard Ages
Child
Sexes Eligible for Study
ALL
Locations
No.of Trial Sites
6
Locations
Netherlands,United States,Italy,United Kingdom
Regulatory Information
Has US IND
True
FDA Designations
Fast Track, Orphan Drug Designation, Rare Pediatric Disease Designation
Recent Updates
First patient randomized 2/2024
Resources/Links
Clinical Publications
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome
Hematopoietic Stem- and Progenitor-Cell Gene Therapy for Hurler Syndrome
News and Press Releases
Orchard Therapeutics Receives U.S. FDA Fast Track Designation for OTL-203 in MPS-IH
Preclinical Publications
Gene therapy augments the efficacy of hematopoietic cell transplantation and fully corrects mucopolysaccharidosis type I phenotype in the mouse model
Protocol
Clinical Trial Protocol
Related NCTID
Phase 1/2: NCT03488394