Angiotech's New Partnering Model for the Convergence Era

Angiotech Pharmaceuticals, a company that has grabbed the new paradigm of convergence by both horns, has amassed intellectual property on drugs and acquired a broad array of biomaterials. Now, to access innovative medical devices, it has embarked upon a new partnering model, and the agreement that it just signed with CABG Medical is only the first example of its new style of dealmaking.

While the major pharmaceutical and medical device companies, apart from their drug-eluting stent projects, continue to sit somewhat on the sidelines of the convergence melee, mid-sized Angiotech Pharmaceuticals Inc. (with 2004 sales of $130 million from its shares of royalties on the Boston Scientific Corp. Taxus drug-eluting stent [See Deal]) has jumped in with both hands and feet. Speaking in mid-March at "Convergence: The Drug/Device Summit," a conference organized by Bio, AdvaMed, the Pittsburgh Life Sciences Greenhouse and MedTech Insight, Windhover Information Inc., Angiotech's chief business officer Jeanne Bertonis articulated the company's strategy to bring biological solutions to bear on the shortcomings of device interventions.

That mandate sounds like it encompasses an overwhelming breadth of applications for a company that's not large, but Bertonis explains...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight 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 Combination Products

Consumer Healthtech Investment Totaled $4.5BN In 2024, But Bar Is High Amid Economic Uncertainty

 
• By 

Global investment in consumer healthtech increased by 9% year-over-year in 2024, totaling $4.5bn, with significant interest in mental health solutions, according to Galen Growth. While the first quarter of 2025 saw raised confidence and investments, the Trump administration’s new tariffs and sweeping changes to healthcare have introduced new uncertainties.

US FDA Should Regulate ‘Dangerous’ Prescription Software Platform As A Medical Device, Says Patient Advocacy Group

The Doctor Patient Forum says the US FDA should regulate a scoring platform from Bamboo Health intended to help clinicians calculate risk for opioid abuse as a medical device to ensure patient safety.

Recall Alerts For Boston Scientific, Philips, J&J, And More

 
• By 

The US FDA has announced seven device safety actions in recent days. The most serious, which relates to a manufacturing defect in Boston Scientific’s Accolade pacemaker, has been linked to 832 injuries and two deaths.

EU Pilots Streamlined Approach To Multinational Combination Product Trials

 
• By 

EU regulators have approved a strategy to streamline the submission and approval of studies that involve the simultaneous investigation of a medicinal product, an IVD, and/or a medical device. The strategy involves rolling out seven cross-sector projects over the next few years.

More from Device Area

FDA Drops Package Labeling Guidance For Hernia Mesh Manufacturers

 

The US FDA recently published a draft guidance document for manufacturers of mesh products that are used during several types of hernia repair procedures.

Medtech Innovators Court London-Based Investors At BioWales 2025

 
• By 

BioWales in London 2025 showcased the efforts healthtech innovators are making to meet investors on their own turf, illustrating changing attitudes and evolving needs.

Somnee AI-Powered Sleep Wearable Raises $10M Seed Round

 

The $10m seed extension funding round will be used to launch the second-generation wearable headband with the added SmartSleep AI operating system.