Data from a pre-specified interim analysis of the Phase 3 study in people with one F508del mutation and one minimal function mutation showed a mean absolute improvement in ppFEV1 of 13.8 percentage points from baseline at week 4 of treatment compared to placebo (p
Spinogenix reports approval of 'tazbentetol' as non-proprietary name for SPG302
Polarean expands XENOVIEW 3T Coil access with Philips compatibility
Immedica gets UAE approval for Zepzelca maintenance treatment
AstraZeneca to invest USD2bn in major Maryland manufacturing expansion
Nuvalent's zidesamtinib NDA filing accepted by US FDA
BioNet receives positive opinion from EMA for VacPertagen marketing authorisation in EU