drugset / Trial / NCT03404024

Safety and Efficacy Study of Gene Therapy for Acute Myocardial Infarction in Korea

NCT03404024 ↗

Phase 2 Withdrawn Helixmith Co., Ltd.
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

EvaluationDrugModalityDoseRoute
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