Can Avanzanite accelerate NHS access to rare disease medicines in the UK?
Avanzanite appoints Sarah O'Connell to expand UK rare disease operations. The move strengthens its European commercialisation and patient access strategy.
Avanzanite appoints Sarah O'Connell to expand UK rare disease operations. The move strengthens its European commercialisation and patient access strategy.
Enhertu wins EU approval after cutting invasive recurrence or death risk by 53% versus T-DM1. Lung toxicity remains a key consideration.
Pfizer wins FDA approval for TALZENNA plus XTANDI in earlier metastatic prostate cancer. See how a 52% progression-risk reduction changes treatment.
Bayer's LYNKUET showed improved self-reported sleep quality in a post-hoc Phase 3 analysis. The findings do not establish a separate sleep indication.
Aptar Pharma acquires Pulmotree to advance Kolibri inhaler technology for complex medicines. Commercial success depends on validation and adoption.
Mirum's ATEBRIOZ reduced abnormal bone volume in children aged 6 to under 12 with FOP. Can the results support FDA label expansion in 2027?
AimedBio's BI 4060107 enters Phase 1 testing under a potential $991 million Boehringer Ingelheim deal. Safety and early activity remain unproven.
Serapha Bio's SERP-01 gene editing restores protective protein levels in four AATD patients. Explore the early results and Phase 2/3 plans.
Oruka Therapeutics' ORKA-001 achieves 61% complete skin clearance in Phase 2b psoriasis testing. Explore the results and Phase 3 plans.
Frontier's FMC-376 achieved a 56% response rate in 18 evaluable lung cancer patients, including prior KRAS inhibitor users. Can larger trials confirm benefit?