Skip to main content
  • Clinical
      |Clinical
    • Acute Coronary Syndromes
    • Cardiac Surgery
    • Covid-19
    • Heart Failure
    • Heart Health
    • Heart Rhythm
    • Hypertension
    • Interventional Cardiology
    • Mitral Valve
    • Pharmaceutics
    • Structural Heart Disease
    • TAVR
    • Tricuspid Valve
    • Vascular & Endovascular
  • Management
      |Management
    • Chest Pain Guidelines
    • Compensation
    • Economics
    • Education & Training
    • Legal News
    • Patient Care
    • Policy & Regulations
    • Professional Associations
    • Quality
    • Revenue
    • Staffing
  • Technology
      |Technology
    • AI
    • Cardiac Imaging
    • Cath Lab
    • CT
    • CVIS
    • ECG
    • Echo
    • EP Lab
    • Informatics
    • MRI
    • Nuclear Cardiology
    • Remote Monitoring
  • Videos
  • Conferences
      |Conferences
    • ACC
    • AHA
    • ASE
    • ASNC
    • ESC
    • EuroPCR
    • HFSA
    • HRS
    • HRS
    • SCAI
    • SCCT
    • SIIM
    • SNMMI
    • STS
    • TCT
    • VIVA
  • Custom Content
      |Custom Content
    • Experience Stories
    • Webinars & Videos
  • Subscribe
  • Forty Under 40 Award
      |Forty Under 40 Award
    • Class of 2026
    • Class of 2025

Search form

Home

Roche spends $2.7B to acquire biotech company with multiple obesity, diabetes drugs in development

healthcare money economics dollar stethoscope acquire merger

Roche, one of the world’s largest pharmaceutical companies, will gain both oral and injectable assets as a result of this acquisition.

  • Read more about Roche spends $2.7B to acquire biotech company with multiple obesity, diabetes drugs in development

FDA approves early feasibility study for total artificial heart technology

BiVACOR Total Artificial Heart. BiVACOR, an international medical device company with headquarters in the United States and Australia, has received approval from the U.S. Food and Drug Administration (FDA) to kick off an early feasibility study (EFS) for its total artificial heart (TAH) technology.

Graphics courtesy of BiVACOR.

The device is intended to be a bridge for heart failure patients waiting to receive a full heart transplant.

  • Read more about FDA approves early feasibility study for total artificial heart technology

New AFib guidelines include higher recommendations for catheter ablation, LAAO

2024 has been a banner year for structural heart treatments, especially those focused on the tricuspid valve. In February, for example, Edwards Lifesciences made history when its Evoque transcatheter tricuspid valve replacement (TTVR) system became the first device of its kind to gain U.S. Food and Drug Administration (FDA) approval for treating tricuspid regurgitation (TR). Two months later, Abbott’s TriClip transcatheter edge-to-edge repair (TEER) system also gained FDA approval for the treatment of TR.

Cardiologists, electrophysiologists, surgeons and patient representatives all worked together on the updated guidelines, which were published in both the Journal of the American College of Cardiology and Circulation.

  • Read more about New AFib guidelines include higher recommendations for catheter ablation, LAAO

First US patient treated with Medtronic’s FDA-approved renal denervation system

The Medtronic Symplicity Spyral Renal Denervation system uses a catheter that curls in the renal artery to place radiofrequency electrodes against the vessel wall to ablate the nerves that control vasodilation, so the artery can be propped in the fully open position.

The Symplicity Spyral RDN system. Graphic courtesy of Medtronic.

Interventional cardiologist David Kandzari, MD, performed the procedure just days after the device received full FDA approval. 

  • Read more about First US patient treated with Medtronic’s FDA-approved renal denervation system

‘We should halt this practice’: Common hormone treatment for donated hearts may be harmful

Tiny fragments of plastic are commonly found deep inside the human body. Heart surgery, it seems, is one of many ways these microplastics are reaching their destination.  Surgeons Operating On Patient

"This practice has been adopted by multiple organ-procurement organizations and is used on thousands of organ donors each year, without ever having been rigorously studied," one researcher said. 

  • Read more about ‘We should halt this practice’: Common hormone treatment for donated hearts may be harmful

Johnson & Johnson acquires medical device company behind new LAA technology for $400M

business news announcement

The deal could also include additional clinical and regulatory milestone payments in the years ahead.

  • Read more about Johnson & Johnson acquires medical device company behind new LAA technology for $400M

Cardiologist receives $7M for 5-year study to boost care for heart failure patients

smartphone_elderly.jpg

The research will focus on ways to improve the utilization of electronic resources among heart failure patients and the doctors who treat them.

  • Read more about Cardiologist receives $7M for 5-year study to boost care for heart failure patients

Avidity Biosciences inks drug discovery deal worth up to $2.3B with industry heavyweight

Avidity Biosciences, a San Diego-based biopharmaceutical company, is expanding its ongoing collaboration with Bristol Myers Squibb to identify new cardiovascular therapies.

  • Read more about Avidity Biosciences inks drug discovery deal worth up to $2.3B with industry heavyweight

Robotic-assisted CABG reduces healthcare costs, primarily thanks to shorter hospital stays

money business cash flow dollar. Kingsway Financial Services, a Chicago-based holding company with subsidiaries in several industries, has acquired New Jersey-based Digital Diagnostics Imaging (DDI) for $11 million. The transaction was funded with $5.4 million in cash and $5.6 million in debt financing.

The technology may not be cheap, but new research published in The American Journal of Cardiology suggests the investment is well worth it. 

  • Read more about Robotic-assisted CABG reduces healthcare costs, primarily thanks to shorter hospital stays

New formula could mean diabetes and weight loss drugs such as semaglutide are only needed every 4 months

Weekly doses of semaglutide, a GLP-1 receptor originally developed to treat diabetes, could help approximately 93 million U.S. adults lose weight and reduce their risk of adverse cardiovascular events, according to new research published in Cardiovascular Drugs and Therapy. Novo Nordisk sells and markets subcutaneous treatments of semaglutide 2.4 mg under the brand name Wegovy.

GLP-1 agonists are often taken as daily or weekly injections. A new delivery system could help make it so those same drugs are only required three times per year. 

  • Read more about New formula could mean diabetes and weight loss drugs such as semaglutide are only needed every 4 months

Pagination

    • First page « First
    • Previous page ‹ Previous
    • Page …261
    • Page 262
    • Page 263
    • Page 264
    • Current page 265
    • Page 266
    • Page 267
    • Page 268
    • Page 269 …
    • Next page Next ›
    • Last page Last »
Subscribe
  • Home
  • News
  • Article Archive
  • Custom Content
  • Webinars
  • Press Releases
  • Content Studio
  • Advertising
  • Submit Press Release
  • Contact Us
  • Terms of Use
  • Privacy Policy
  • Cardiovascular Business
  • HealthExec
  • Radiology Business
  • Press Releases
  • Submit Press Release
© 2026 Innovate Healthcare | All Rights Reserved. | Terms of Use | Privacy Policy
Design by Adaptive Theme