Neovasc is a leader in the development of minimally invasive transcatheter mitral valve replacement technologies, and minimally invasive devices for the treatment of refractory angina. The company currently has two devices. The Reducer is CE-marked in the European Union and under FDA review for the treatment of refractory angina. The Reducer provides relief of angina symptoms by altering blood flow in the heart’s circulatory system, thereby increasing the perfusion of oxygenated blood to ischemic areas of the heart muscle. Tiara is a self-expanding mitral bioprosthesis for treatment of mitral valve regurgitation (“MR”) by replacing the diseased valve.
Conventional surgical treatments are only appropriate for about half of MR patients, who number an estimated four million in the U.S. with a similar number of patients in Europe. Tiara is implanted using a minimally invasive, transcatheter approach which avoids open-heart surgery or use of a cardiac bypass machine. The Tiara valve is not commercially available and is currently being evaluated in two ongoing clinical trials in the US, CA, Europe and Israel.
Financial Reports
Latest News
Neovasc Announces Third Quarter 2021 Financial Results and Provides Corporate Update
Neovasc Announces FDA Advisory Panel Result on Neovasc Reducer Medical Device for the Treatment of Refractory Angina
Neovasc to Report Third Quarter Financial Results on November 5, 2020
Presentation and Events
2020 Annual General Meeting
August 2020 Presentation
Q2 Earnings Call
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Auditor
Grant Thornton LLP, Vancouver, BC
Legal Counsel
Blakes LLP, Vancouver, BC
Transfer Agent
Computershare, Vancouver, BC
Investor Relations
Chris Clark, Chief Financial Officer
investors@neovasc.com