drugset / Trial / NCT00438867
Angiogenesis in Women With Angina Pectoris Who Are Not Candidates for Revascularization
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ad5FGF-4 | Unknown | — | Other |