drugset / Trial / NCT01157871

Dose-finding, Safety and Efficacy Study of NV1FGF in Patients With Intermittent Claudication

NCT01157871 ↗

Phase 2 Completed 36 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective is to assess safety and efficacy of two different doses of NV1FGF as compared to placebo. The secondary objective is to assess the pharmacokinetics of NV1FGF and FGF-1 protein.

Timeline

Start
2004-06
Primary completion
2005-08
Completion
2005-08

Drugs

EvaluationDrugModalityDoseRoute
Subject riferminogene pecaplasmid Other / unclassified 4 mg Intramuscular
Subject riferminogene pecaplasmid Other / unclassified 8 mg Intramuscular