drugset / Trial / NCT00068133

Trial of VLTS-589 in Subjects With Intermittent Claudication

NCT00068133 ↗

Phase 2 Completed 100 enrolled Valentis
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of VLTS-589 compared with placebo, administered bilaterally to the lower extremities, in subjects with intermittent claudication and to determine the effect of VLTS-589 in peak walking time (PWT) for subjects receiving VLTS-589 compared with subjects receiving placebo.

Timeline

Start
2003-06
Primary completion
—
Completion
2005-06

Drugs

EvaluationDrugModalityDoseRoute
Subject VLTS-589 Other / unclassified — —