drugset / Trial / NCT03068585

Efficiency, Safety and Portability of Neovasculgen

NCT03068585 ↗

Phase 2/3 Completed 100 enrolled Artgen Biotech
RandomizedParallel-groupOpen-labelTreatment

Summary

In 2010, we completed a phase 1 to 2a clinical trial of pCMV-vegf165 in patients with chronic lower limb ischemia (stage 2a to 3 according to Fontaine classification modified by A. V. Pokrovsky) who were not suitable for reconstructive surgery or endovascular treatment. This study demonstrated the safety, feasibility, and short-term(3 months) efficacy of pCMV-vegf165 gene transfer,12,13which lead to conducting a phase 2b to 3 multicenter clinical trial. The study was conducted under the control of the Russian Ministry of Health and was completed in 2011. Patients enrolled in the study were subjected to a 6-month

Timeline

Start
2010-02
Primary completion
2011-06-01
Completion
2011-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Neovasculgen Other / unclassified 1.2 mg Intramuscular