Contact SCGE




Gene Therapy Trial Report

Summary

A Study of the Safety and Efficacy of Prime Editing (PM359) in Participants With p47phox Autosomal Recessive Chronic Granulomatous Disease (CGD )


NCTID NCT06559176 (View at clinicaltrials.gov)
Description
Development Status Inactive
Indication Chronic Granulomatous Disease
Disease Ontology Term DOID:0070192
Compound Name PM359
Sponsor Prime Medicine, Inc.
Funder Type Industry
Recruitment Status
Active not recruiting
Enrollment Count 12 (ESTIMATED)
Results Posted Not Available

Therapy Information


Target Gene/Variant NCF1 (c.75_76delGT)
Therapy Type Gene editing
Therapy Route Ex-vivo
Mechanism of Action Mutation correction
Route of Administration Intravenous
Drug Product Type Autologous cells
Target Tissue/Cell CD34+ cells
Delivery System Electroporation
Vector Type
Editor Type prime editor
Dose 1 Transduced CD34+ cells
Dose 2
Dose 3
Dose 4
Dose 5

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2024-07-11
Completion Date 2030-02
Last Update 2025-05-25

Participation Criteria


Eligible Age >=6 Years
Standard Ages Child, Adult, Older adult
Sexes Eligible for Study ALL

Locations


No.of Trial Sites 5
Locations Canada,United States,United Kingdom

Regulatory Information


Has US IND True
FDA Designations Orphan Drug Designation, Rare Pediatric Disease Designation
Recent Updates Prime is shelving this program due to market considerations, may seek a partner for continued development

Resources/Links