Helsinn And BridgeBio Ink Infigratinib Cancer Pact

Duo Will Co-develop And Commercialise FGFR1-3 inhibitor In Oncology

Helsinn’s strategic collaboration with BridgeBio Pharma to co-develop and commercialise candidate FGFR1-3 inhibitor infigratinib in oncology will give the Swiss family-owned company its first targeted cancer therapeutic for the US market, its CEO tells Scrip.

Helsinn Handshake
BridgeBio retains full rights to infigratinib for use in skeletal dysplasias • Source: Shutterstock

Switzerland-based Helsinn Group hopes to market its first targeted cancer therapy in the US though a newly agreed global collaboration and licensing pact with BridgeBio Pharma, Inc. to jointly develop and commercialize the latter’s FGFR1-3 inhibitor, infigratinib.

Under the collaboration, announced 31 March, BridgeBio’s affiliate QED Therapeutics and Helsinn plan to co-commercialize infigratinib for oncology and...

Scrip Podcast

Keep up with the top pharma business news of the week. On the go.

Scrip brings you a weekly bulletin of top picks.

More from Deals

More from Business

  • How A New Healthcare Dialogue Is Driving Market Access In Mexico

    Companies stand a better chance of securing public reimbursement in Mexico for innovative medicines if they understand changing approaches to healthcare. The shift means the emergence of managed entry agreements and a focus on economic impact, explains AMIIF, Mexico's research-based pharmaceutical industry association.

  • How Novartis Is Elevating CVD Outcomes, Driving ‘Personalized Access’ In APMA

    Novartis’s APMA chief outlines the company’s tailored approach to deliver long-term outcomes, novel access solutions via innovative financing options and shape the CVD disease ecosystem in the extraordinarily diverse region. Partnering to build AI infrastructure is another key prong.

  • India Rare Diseases: Court Shows Path For Policy Action, Funding, Price Issues-- Test-2

    A court order encompassing funding, drug pricing, clinical trials and overall policy implementation aspects is expected to bring about a paradigm shift in the treatment of rare diseases in India. Sarepta, Roche and Sanofi are among the key players that have been part of pricing discussions.