drugset / Trial / NCT00438867

Angiogenesis in Women With Angina Pectoris Who Are Not Candidates for Revascularization

NCT00438867 ↗

Phase 3 Unknown 300 enrolled Cardium Therapeutics
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether a one-time intracoronary infusion of Ad5FGF-4 is effective in reducing the time to onset myocardial ischemia as measured by exercise treadmill testing and improving myocardial blood flow as measured by SPECT imaging. Exercise capacity, angina functional class, patient symptoms and quality of life will also be evaluated to characterize the efficacy of Ad5FGF-4. Short-term and long-term safety of Ad5FGF-4 will also be evaluated.

Timeline

Start
2007-05
Primary completion
2009-11
Completion
—

Outcome

Missed primary endpoint

paper interim analysis of the AGENT-3 trial indicated that the primary end point change from baseline in total ETT time at 12 weeks would not reach significance. PMID 17825712 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ad5FGF-4 Unknown — Other