Gene Therapy for the Treatment of Chronic Stable Angina

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of catheter based injections of VM202 into the heart.

Clinical Trial Description

A phase I/II, open label, dose-escalation, multicenter, 12 month study designed to assess the safety and tolerability of catheter based percutaneous myocardial injection of VM202 in patients with chronic refractory myocardial ischemia. The study will consist of three (3) cohorts with a total of 4 subjects enrolled in each cohort. Endocardial injections will be performed with the MyoStar Injection Catheter under guidance of the NOGA XP Cardiac Navigation System. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01002495
Study type	Interventional
Source	Helixmith Co., Ltd.
Contact
Status	Withdrawn
Phase	Phase 1/Phase 2
Start date	March 2015
Completion date	January 2016

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