GSK has announced that the US FDA has accepted for priority review a supplemental Biologics License Application for Jemperli ...
A July 2026 Leerink Partners report named Carterra a core enabling technology in the growing Lab‑in‑the‑Loop market. The ...
Erasca has been granted Fast Track Designation by the FDA for ERAS‑0015, an oral pan‑RAS molecular glue being developed for ...
Avulux has received De Novo marketing authorisation from the FDA, establishing the first recognised device classification for ...
Lundbeck has secured orphan designation from the European Commission for asedebart, its investigational anti‑ACTH monoclonal ...
AC Immune has announced encouraging preliminary findings from its phase 1 first‑in‑human study of ACI‑19764, an orally ...
VarmX has enrolled the first participant in its global phase 3 EquilibriX S trial evaluating VMX C001 for the rapid ...
FairJourney Bio has published a peer‑reviewed study in mAbs describing a novel antibody‑engineering approach designed to ...
The MHRA’s position is that MBMPs fall within the scope of the existing UK medicines regulatory framework set out in the ...
Teva Pharmaceuticals has announced that the US Food and Drug Administration has accepted the new drug application for ...
NICE has recommended Axhidrox (glycopyrronium bromide) cream for routine NHS use in adults with severe primary axillary hyperhidrosis whose symptoms are not adequately controlled with lifestyle advice ...
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