The funding will be used to complete the Phase II/III trial of ulviprubart, and to support commercial launch preparation.
GlobalData’s Revati Tatake discussed key trends in biopharma which are set to have an impact in 2025 and beyond.
Lundbeck has received the US FDA fast track designation for amlenetug, a potential treatment for multiple system atrophy (MSA ...
The US Food and Drug Administration (FDA) has approved SpringWorks Therapeutics’ Gomekli (mirdametinib) to treat ...
EC has granted marketing authorisation to BridgeBio Pharma’s acoramidis under the Beyonttra brand name for treating ATTR-CM.
Health Canada has approved MSD’s anti-programmed cell death protein 1 (PD-1) therapy Keytruda for treating adults with ...
Travere’s stock price climbed by 14% following the announcement it will seek an FDA label expansion for Filspari.
Being realistic, responsive and transparent is key in engaging unresponsive and underperforming clinical trial sites; that ...