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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
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