Coronary/Structural Heart

BridgeBio Pharma Announces Submission of New Drug Application (NDA) to U.S. Food and Drug Administration (FDA) for Acoramidis for the Treatment of Patients with Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

PALO ALTO, Calif., Dec. 05, 2023 (GLOBE NEWSWIRE) — BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a commercial-stage biopharmaceutical company focused on genetic diseases and cancers, today announced that it has submitted an NDA for acoramidis to the U.S. FDA for the treatment of ATTR-CM. The application was based […]

Colibri’s transcatheter aortic valve [TAVR] EU pilot study validates its pre-mounted, pre-packaged, dry tissue, ready-to-use balloon-expanded valve with demonstration of superior hemodynamics

LOUISVILLE, Colo., Dec. 1, 2023 /PRNewswire/ — The initial findings of Colibri Heart Valve’s multicenter high-risk TAVR EU pilot study were presented at PCR London Valves November 20th, 2023. The study was conducted by CERC (Centre Européen de Recherche Cardiovasculaire) as acting CRO (clinical research organization).
Speaking on behalf of the study’s team of investigators, Dr Bernard Chevalier, principal investigator, L’hôpital Privé Jacques Cartier, Massy, France, presented the primary 30-day endpoint results of the trial in the 26 patients, classified at high-risk for surgical aortic valve replacement, who received the Colibri dry tissue TAVR valve utilizing the pre-mounted, pre-packaged delivery system. All patients survived to the initial 30-day milestone. Central core laboratory measurements indicated notably high measures of hemodynamic valve performance, including mean valve area of 2.23 cm2 and mean Doppler index of 0.56 at 30 days.
The report represents major clinical validation of Colibri’s ground-breaking, world’s first TAVR system utilizing a pre-mounted, pre-packaged, dry tissue, ready-to-use balloon-expanded valve and system design that does not involve mounting of the valve prosthesis in the catheterization laboratory. The hemodynamic performance of Colibri’s unique, innovative leaflet design appears to surpass that of predicate balloon-expanded TAVR valves.
Professor David Hildick-Smith, Head of Structural Heart Disease at the University Hospitals Sussex in Brighton, UK, said “The Colibri pre-mounted TAVI system is very straightforward and efficient. It comes preloaded in its packaging – just like a coronary stent does. We can take the system directly from its packaging and implant it in the patient. There is no need for valve crimping, loading, or other technical assistance. Furthermore, and crucially, the valve area obtained is significantly greater than with other valve systems, and this may prove very advantageous in terms of symptom resolution and valve durability.”
Colibri believes these results provide strong validation of its innovative pre-mounted TAVR valve—the first truly ready-to-use valve system that will set a new standard in structural heart technology, and the company now looks forward to launching its FDA feasibility trials.
About Colibri Heart Valve:
Colibri Heart Valve LLC (“Colibri”) is a privately held medical device company that researches and develops novel, patent protected, structural heart technologies. Colibri was formed in 2010 and through its proprietary tissue technology and valve design, Colibri has developed a pre-mounted, pre-crimped, and pre-loaded, Ready-for-Use balloon expandable transcatheter aortic valve implantation (TAVI) system called the “Colibri TAVI System.” The Colibri technology is protected by both trade secrets and issued and pending patent applications with priority claims and content dating back to January 4, 2002. https://www.colibrihv.com
For more information please contact:
Thomas Wolf 303-808-2570.
SOURCE Colibri Heart Valve

Procyrion Announces First Patient Enrollments in the DRAIN-HF Pivotal IDE Trial for Aortix™ Percutaneous Mechanical Circulatory Support Technology

Technology to be evaluated in acute decompensated heart failure patients, where current treatment options remain ineffective and lacking HOUSTON, Nov. 30, 2023 /PRNewswire/ — Procyrion, Inc., a medical device company dedicated to improving outcomes for patients with cardiac and renal…

ReValve Solutions Announces Successful First-in-Human Trial with Next-Generation Technology for Transcatheter Mitral Valve Replacement

IRVINE, California–(BUSINESS WIRE)–ReValve Solutions Inc. (ReValve), que ha desarrollado una tecnología de nueva generación para facilitar el reemplazo transcatéter de la válvula mitral, dio a conocer que un hombre de 81 años, con antecedentes de insuficiencia cardiaca, una serie de injertos quirúrgicos de by-pass fallidos y regurgitación de la válvula mitral grave (RM 4+), fue tratado con éxito con el sistema de Palmetto. El procedimiento de reemplazo transcatéter de la válvula mitral de últ

PlaqueTec recruits first ten patients in BIOPATTERN trial

CAMBRIDGE, England–(BUSINESS WIRE)–PlaqueTec, a company identifying endotype-specific biomarkers to advance precision medicine for coronary artery disease (CAD), today announced that it has received the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) approval to continue its BIOPATTERN trial following recruitment of the first ten patients with CAD. The trial has been designed to improve understanding of the pathobiology of atherosclerotic cardiovascular diseases (ACVD) and how

SUPIRA MEDICAL, INC., A SHIFAMED PORTFOLIO COMPANY, RECEIVES FDA BREAKTHROUGH DEVICE DESIGNATION AS THE COMPANY CLOSED $40M IN SERIES D FINANCING

LOS GATOS, Calif., Nov. 21, 2023 /PRNewswire/ — Supira Medical, Inc., a Shifamed portfolio company, announced today that it has received U.S. Food and Drug Administration (FDA) breakthrough device designation for its Supira System, a next-generation percutaneous ventricular assist device (pVAD). This approval comes as the company closed $40M in Series D financing and prepares […]

Arineta Receives FDA Clearance for its Deep Learning Image Reconstruction Technology in SpotLight™ Cardiovascular CT Scanners

Caesarea, Israel – November 20, 2023 – Arineta Cardio Imaging, a leader in point-of-care cardiovascular CT solutions, today announced 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its deep learning image reconstruction (DLIR) technology for use in its SpotLight™ family of cardiovascular CT (CCT) scanners. This next-generation […]

Teleflex Announces First Patient Enrollment in ACCESS-MANTA™ Registry

Registry Intends to Examine Contemporary On-Label Use of the MANTA™ Vascular Closure Device Including Appropriate Patient Selection and Proper Vascular Access WAYNE, Pa., Nov. 16, 2023 (GLOBE NEWSWIRE) — Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the first patient enrollment in a clinical registry […]