BioVentrix
8
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2
3
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
High Risk
Score: 85/100
25.0%
2 terminated/withdrawn out of 8 trials
60.0%
-26.5% vs industry average
0%
0 trials in Phase 3/4
0%
0 of 3 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (8)
RELIVE (Randomized Evaluation of Less Invasive Ventricular Enhancement) Trial
Role: lead
Randomized Evaluation and Verification of Ventricular Enhancement
Role: lead
ALIVE Expended Access - Clinical Study
Role: lead
BioVentrix Revivent TC™ System Clinical Study
Role: lead
Study Tests Whether a Standardized LVR Performed With the Blue Egg Device Improves Cardiopulmonary Exercise Capacity
Role: lead
Clinical Study of the BioVentrix Revivent TC for the Treatment of Ischemic Cardiomyopathy
Role: lead
Prospective Study of the BioVentrix PliCath HF™ System for the Treatment of Ischemic Cardiomyopathy
Role: lead
Safety and Efficacy Study of the BioVentrix PliCath HF System
Role: lead
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