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BMS strikes $14bn deal for Karuna Therapeutics

European Pharmaceutical Review

KarXT targets both the M1 and M4 muscarinic receptors, resulting in a differentiated safety and efficacy profile. Currently under review by the US Food and Drug Administration (FDA), KarXT is expected to launch in the US in late 2024.

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First multiple sclerosis biosimilar approved in Europe

European Pharmaceutical Review

This recent decision by the EC follows approval of Tyruko ® (natalizumab) by the US Food and Drug Administration (FDA) last month for the same indication. Polpharma Biologics will maintain responsibilities for development of medicine, manufacturing and supply of drug substance.

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AI in Healthcare 2025: Navigating New Frontiers in Innovation and Regulation

Nixon Gwilt Law

Venture investment skyrocketed, partnerships between leading AI startups and health systems took shape, and policymakers across the globe grappled with AIs implications for consumer safety and algorithmic transparency. Want to stay up to date on the latest changes in statewide regulatory changes?