The upcoming EpiPen patent expiration on 11 September 2025 sets the stage for a pivotal shift in the epinephrine delivery market.

CorMedix, a biopharmaceutical company specialising in critical care products, is to acquire Melinta Therapeutics for $300m.

The FDA’s new PreCheck programme is aimed at facilitating the introduction of new US drug manufacturing facilities.

The US Food and Drug Administration (FDA) has lifted a pause in the use of Valneva’s chikungunya vaccine Ixchiq in older adults after a benefit-risk reevaluation, though the move comes with an ...

Primary packaging is never an afterthought in the world of injectable drugs, where systems such as vials, syringes, and ...

Gilead's PrEP Yeztugo is set to become the pharma's star asset, with GlobalData forecasting of just under $5bn in 2031.

Linked data could unlock essential hidden insights across healthcare – but linking has to be executed correctly to avoid ...

The health secretary has halted the development of 22 mRNA vaccine projects by BARDA while stopping all future schemes.

Genmab and AbbVie’s Epkinly has met its dual primary endpoints as a second-line combination therapy in relapsed/refractory follicular lymphoma (FL).

The US FDA has given accelerated approval to Jazz Pharma for Modeyso to treat adult and paediatric patients with diffuse midline glioma.

MAXONA Pharmaceuticals has submitted an IND application seeking approval from the US FDA for its lead compound, MAX-001, to treat acute pain.

Astria has made an exclusive licensing agreement with Kaken for the development and commercialisation rights of navenibart in Japan.