drugset / Trial / NCT03404024
Safety and Efficacy Study of Gene Therapy for Acute Myocardial Infarction in Korea
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the safety and clinical efficacy of VM202RY injected via transendocardial route using C-Cathez® catheter (Celyad, S.A., Belgium) in subjects with AMI. * Stage 1: Evaluation of safety and tolerability of VM202RY injection * Stage 2: Evaluation of safety and efficacy of VM202RY injection
Timeline
- Start
- 2018-01-25
- Primary completion
- 2019-08-20
- Completion
- 2019-08-20
Outcome
Outcome not reported
Stopped: “Company decided not to move forward with this study.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | VM202RY | Unknown | 0.5 mg | Other |
| Subject | VM202RY | Unknown | 1 mg | Other |
| Subject | VM202RY | Unknown | 1.5 mg | Other |
| Subject | VM202RY | Unknown | 2 mg | Other |
| Subject | VM202RY | Unknown | 3 mg | Other |