Trials / Recruiting
RecruitingNCT06391736
Evaluation of the Safety and Efficacy of Late-onset Pompe Disease Gene Therapy Drug
A Multi-centered, Single Arm, Open Labeled, Study to Evaluate the Safety, Tolerability, and Efficacy of an Adeno-associated Virus Vector Expressing the Human Acid Alpha-glucosidase (GAA) Transgene Intravenous Injection in Patients With Late-onset Pompe Disease
- Status
- Recruiting
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 33 (estimated)
- Sponsor
- GeneCradle Inc · Industry
- Sex
- All
- Age
- 6 Years
- Healthy volunteers
- Not accepted
Summary
This study is being conducted to evaluate the safety and effectiveness of GC301 adeno-associated virus vector expressing codon-optimized human acid alpha-glucosidase (GAA) as potential gene therapy for Pompe disease. Patients diagnosed with late-onset Pompe disease (LOPD) who are ≥ 6 years old will be studied.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| GENETIC | GC301 | GC301, is an adeno-associated virus 9 (AAV9) vector delivering a functional copy of the human GAA gene |
Timeline
- Start date
- 2024-04-19
- Primary completion
- 2026-12-01
- Completion
- 2026-12-01
- First posted
- 2024-04-30
- Last updated
- 2025-07-03
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06391736. Inclusion in this directory is not an endorsement.