Stent Mania US Style

For the last couple of years, J&J has all but owned the US market for coronary stents, in the process creating an $800 million business with 90-95% market share. But now it's bracing for a host of competitors, including Guidant's much anticipated product.

With the filing by Guidant Corp. of a PMA requesting FDA approval for the use of its coronary artery stent in restenosis, the US stent market is moving one step closer to an all-out battle. Currently, Johnson & Johnson 's Palmaz-Schatz stent has 90% share in the US, where it faces competition only from Cook Group Inc. , whose GR-II is a niche product with a limited indication. The approval of Guidant's Multi-Link, which could come late this year or early next year, is likely to create a whole new ball game. The Multi-Link, which is doing extremely well in Europe, is expected to be the first head-to-head competitor J&J faces in the US. And a strong opponent it will be: the Multi-Link's easier-to-use delivery system, combined with the marketing strength of its maker, has helped it capture the number three position in Europe, say analysts. (Guidant says it is number one in Europe in terms of units, with around 20% market share, despite a recall in France.) Medtronic Inc. just received FDA approval of its Wiktor stent, but only for limited applications.

The big question is what J&J intends to do about defending its patents in the US. Based on the settlement...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on In Vivo for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Archive

Final Chance To Have Your Say: Take Our Reader Survey This Week

 

Editor’s note: This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Early Development Deals: Ipsen's Strategy For Biomarker-Driven Success

 

Mary Jane Hinrichs, Ipsen’s head of early development, talks to In Vivo about getting ahead of the competition by securing deals for candidates before they enter Phase I trials.   

Shape Our Content: Take The Reader Survey

 

Editor’s note: We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in the coverage topics, content format or the method in which you receive and access In Vivo, or if you love it how it is, now is the time to have your voice heard.

In Partnership with Cerba Research

Prioritizing Safety in CAR-T Therapy: Patient Monitoring with Cerba Research’s Testing Portfolio

The cell and gene therapy (CGT) clinical trial landscape in general and CAR-T cell clinical trials in particular are a special focus for the FDA, EMA, and other regulatory agencies. The whole industry is thus aware of the recent FDA safety investigation and requirements for labeling CAR therapy products.

More from In Vivo

Wide Of The Mark: ‘The Worst EU Medtech Predictions Have Not Come True’

 
• By 

Jana Grieb, European regulatory and market access legal expert at McDermott Will & Emery, explains why the healthtech and pharma industries are warming to the new EU health commissioner as he faces calls to make the MDR more “user friendly.”

This Belgian Biotech’s Drug Cocktail Could Help Reverse Muscle Aging

 
• By 

While big pharma pours billions into creating new anti-aging molecules, a Belgian startup has taken a different path: combining existing safe drugs with AI precision. The early results suggest it might be onto something revolutionary.

Rising Leaders 2025: Doxie Jordan, From UNC Graduate To Global Market Strategist

 
• By 

Bristol Myers Squibb executive Doxie Jordan discusses his path to global commercial leadership and the principles guiding pharmaceutical market strategy