Arrowhead’s plozasiran clears CHMP: what a positive opinion for FCS means for siRNA’s regulatory arc in Europe
Plozasiran clears CHMP but the real test is reimbursement. Europe's HTA bodies will now decide whether clinical FCS diagnosis is enough.
Plozasiran clears CHMP but the real test is reimbursement. Europe's HTA bodies will now decide whether clinical FCS diagnosis is enough.
Merck cleared one deal hurdle. TERN-701 still has to prove whether chronic myeloid leukemia can justify a $6.7 billion bet.
Eliquis faces pricing pressure, but Bristol Myers Squibb and Pfizer are moving first. Direct access may become pharma’s new defence.
Pediatric heart failure lacks durable LVAD choices. BrioHealth’s Brio4Kids trial now tests whether BrioVAD can narrow that gap.
Customized implants are moving from niche to surgical workflow. CGBIO’s U.S. clearance tests whether speed can become a medtech edge.
Find out how Vapotherm’s FDA-cleared All Patient Circuit could simplify high velocity therapy from neonatal to adult care.
Find out how Sonorous Neurovascular’s BosCATH FDA clearance strengthens its neurovascular access strategy today!
LEVI-04 Phase II data from Levicept Ltd. signal a shift in osteoarthritis treatment. Discover what this means for disease-modifying therapies.
Discover how Novartis Pharma AG is targeting neonatal malaria with Coartem Baby and what WHO prequalification means for global access.
Novartis Pharma AG’s Itvisma gains CHMP support in SMA. Find out how gene therapy could reshape treatment for older patients in Europe.