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BioWorld - Friday, May 1, 2026
Home » Topics » Disease categories and therapies » Cardiovascular

Cardiovascular
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Acqmap system components

Acutus restructures to focus product development activities

Jan. 20, 2022
By Annette Boyle
Acutus Medical Inc. provided highlights of a corporate restructuring along with preliminary unaudited revenues for the fourth quarter and year ended Dec. 31, 2021. The company “will prioritize maximizing console utilization and procedure volume growth in targeted geographic regions as well as a more focused scope of product development initiatives.” The restructuring will include the layoff of more than 50 staff members and reduction of manufacturing costs designed to produce annualized operating expense savings of $23 million to $25 million in 2022.
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3D illustration of heart cross section

Peijia Medical acquires China rights to Jenavalve’s TAVR products for aortic valve diseases

Jan. 18, 2022
By Doris Yu
Peijia Medical Ltd. has acquired exclusive rights to Jenavalve Technology Inc.’s transcatheter aortic valve replacement (TAVR) products for the treatment of aortic regurgitation (AR) and aortic stenosis (AS). Suzhou, China-based Peijia is now able to develop, manufacture, and commercialize the TAVR products in Greater China.
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Researchers suggest ZEB2 targeting as an approach for atherosclerosis

Jan. 18, 2022
Pill in immersive interface

AZ delves further into AI, signing deals with Scorpion, Benevolentai

Jan. 13, 2022
By Richard Staines
Astrazeneca plc has announced two significant R&D deals with Scorpion Therapeutics Inc. and Benevolentai Ltd., which it hopes will sharpen its research into cancer, lupus and heart failure. Both of the deals involve artificial intelligence (AI) as a way to increase the probability of success during the clinical development process and reduce the chances of costly trial failures.
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Targeting GNAO1 presents a new therapeutic strategy for heart failure

Jan. 13, 2022
Ensite X EP system consoles

FDA greenlights Abbott’s cardiac mapping platform, boosting its position in EP race

Jan. 12, 2022
By Annette Boyle
Abbott Laboratories received FDA 510(k) clearance for the Ensite X EP system with Ensite omnipolar technology, the company’s cardiac mapping platform. The system, which is used to identify and treat abnormal heart rhythms such as atrial fibrillation, produces detailed three-dimensional maps of the heart to guide physicians performing ablation procedures.
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VCAM-1-targeting polyelectrolyte complex enhances therapeutic efficacy of miR-92a inhibitors in vivo

Jan. 12, 2022
Woman using smartphone
J.P. Morgan Healthcare Conference

Digital health panel looks at women’s health through a wide-angle lens

Jan. 11, 2022
By Annette Boyle
A panel of leaders in women’s health at the 2022 edition of the J.P. Morgan Healthcare Conference addressed the challenges and benefits of digital health and new apps in enabling women to be the “chief medical officers” of their families’ health and to take the necessary steps to improve their own. The panel included moderator Lynne Chou O’Keefe, founder and managing partner of Define Ventures; Apple Inc.’s Vice President of Health Sumbul Ahmad Desai; Veronica Gillispie-Bell, assistant professor, Ochsner Health System; Found CEO Sarah Jones Simmer; Michelle Williams, dean of faculty at the Harvard T.H. Chan School of Public Health; and Tia Inc. CEO and co-founder Carolyn Witte.
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Asia at night from space

GE Healthcare collaborates with Boston Scientific on cardiac care in Southeast Asia

Jan. 11, 2022
By Zhang Mengying
Two med-tech giants GE Healthcare Ltd. and Boston Scientific Corp. are teaming up to expand cardiac care in Southeast Asia. GE Healthcare and Boston Scientific reported plans to collaborate on an end-to-end cardiac care solution offered to cardiac care centers in Southeast Asia. The suite of care offered ranges from diagnostic to percutaneous coronary intervention.
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FDA says Wirion embolic protection device recall a class I event

Jan. 11, 2022
By Mark McCarty
The FDA reported a class I recall of the Wirion embolic protection device by Cardiovascular Systems Inc. (CSI), of St. Paul, Minn., due to reports of nine instances of device malfunction. The agency said the filter portion of the device can be difficult to withdraw under some circumstances and thus lead to separation, although the FDA noted that no deaths have been reported in association with the issue despite the risk of embolization. The FDA’s device center also posted a Jan. 11 notification against the use of two tests by Lusys Labs Inc., of San Diego, for the SARS-CoV-2 virus.
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