Actio Biosciences has closed a Series B financing round, raising $66m for advancing the genetics-driven small molecule ...

BioOrbit CEO Dr Katie King said that pre-clinical studies of the crystals produced in space could start as early as 2026.

NICE said it made every effort to support reimbursement for Kisunla and Leqembi, but found the medicines are “not good value ...

Draig Therapeutics has secured £107m ($140m) in an oversubscribed Series A financing round to treat major neuropsychiatric ...

The FDA has approved Gilead Sciences' injectable product, Yeztugo (lenacapavir), as a pre-exposure prophylaxis (PrEP) against ...

NHS England chair Penny Dash shared her views on European healthcare during a fireside discussion at HLTH Europe in Amsterdam ...

Bavarian Nordic has sold a PRV for $160m, a day after the FDA announced a new scheme utilising the fast-track tickets.

Tisento Therapeutics has received fast track designation from the US Food and Drug Administration (FDA) for zagociguat.

FDA Commissioner Dr Marty Makary tried to allay industry concerns about recent cuts and outlined his agenda for the future.

India has proposed increasing US manufacturing by Indian pharma providers of APIs and the final stages of drug processing ...

Novo Nordisk is looking to partner with digital companies at every stage of the weight loss journey to help patients lose ...