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Degenerative Mitral Valve Disease

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Pipeline Programs
2
Companies
3
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
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Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

2 companies ranked by most advanced pipeline stage

Polares Medical
Polares MedicalCA - Palo Alto
2 programs
Transcatheter mitral valve repairN/A1 trial
Transcatheter mitral valve repairN/A1 trial
Active Trials
NCT04666480Terminated1Est. Dec 2022
NCT04679662Not Yet Recruiting10Est. Dec 2026
Edwards Lifesciences
1 program
Edwards PASCAL SystemN/A1 trial
Active Trials
NCT03706833Active Not Recruiting1,247Est. Jun 2031

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
Polares MedicalTranscatheter mitral valve repair
Polares MedicalTranscatheter mitral valve repair
Edwards LifesciencesEdwards PASCAL System

Clinical Trials (3)

Total enrollment: 1,258 patients across 3 trials

NCT04666480Polares MedicalTranscatheter mitral valve repair

Early Feasibility Study of the PLAR Implant and Delivery System to Treat Degenerative Mitral Regurgitation

Start: Apr 2021Est. completion: Dec 20221 patients
N/ATerminated
NCT04679662Polares MedicalTranscatheter mitral valve repair

EXPLORE DMR: Early Feasibility Study of the PLAR Implant and Delivery System to Treat Degenerative Mitral Regurgitation

Start: Mar 2021Est. completion: Dec 202610 patients
N/ANot Yet Recruiting
NCT03706833Edwards LifesciencesEdwards PASCAL System

Edwards PASCAL CLASP IID/IIF Pivotal Clinical Trial

Start: Nov 2018Est. completion: Jun 20311,247 patients
N/AActive Not Recruiting

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

2 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.