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BioWorld - Thursday, May 7, 2026
Home » Topics » Disease categories and therapies » Cardiovascular

Cardiovascular
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Epeleuton shows efficacy in preclinical models of atherosclerosis

June 3, 2021

ATTR removal observed in vitro and in vivo with NI-006

June 3, 2021

Researchers develop new model of extracorporeal membrane oxygenation thrombosis

June 3, 2021

CIDEC gene silencing ameliorates experimental diabetic cardiomyopathy

June 3, 2021
U.S. intellectual property illustration

Alivecor takes patent dispute with Apple to ITC

June 2, 2021
By Mark McCarty
Alivecor Inc. has elevated its patent dispute with Apple Inc. to the U.S. International Trade Commission (ITC) in a move that could damage the latter’s foray into digital health. Alivecor is alleging that Apple, of Cupertino, Calif., has infringed on Alivecor patents for electrocardiogram monitoring technology, a development that may foreshadow a continuing legal struggle between the two companies for a large and rapidly growing market.
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Acumen HPI software screenshot

FDA OKs Edwards’ HPI software with noninvasive Acumen IQ cuff

June 2, 2021
By Meg Bryant
Edwards Lifesciences Corp. has won the FDA’s nod for its Acumen hypotension prediction index (HPI) software with the Acumen IQ finger cuff. Prior to receiving this 510(k) clearance, the low blood pressure prediction software was only available for patients using an invasive arterial line. The Acumen HPI software uses data gleaned from the Acumen IQ cuff, along with machine learning, to alert clinicians if a patient is at risk of hypotension, drops in pumping pressure that reduce the flow of oxygenated blood and nutrients to the body’s vital organs.
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Phase I data for anti-PCSK9 peptide vaccine candidates AT-04A and AT-06A

June 1, 2021

Bayer presents new alpha2C-adrenoceptor antagonists

June 1, 2021

Ziltivekimab reduces biomarkers of inflammation and thrombosis in phase II RESCUE study

May 31, 2021
3D heart illustration showing tricuspid and bicuspid valves

Micro Interventional Devices scores FDA breakthrough nod for tricuspid regurgitation treatment

May 28, 2021
By Meg Bryant
The FDA has granted breakthrough device designation to Micro Interventional Devices Inc. (MID) for its Mia-T percutaneous tricuspid annuloplasty system. The company will enjoy increased communication with the agency and priority review as it pursues regulatory approval.
Read More
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