FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

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FDA approves updated label for Lilly’s Amyvid (florbetapir F 18 injection) to support diagnosis of Alzheimer’s disease in patients

25 June 2025 -  Eli Lilly announced that the US FDA has approved a label update for Amyvid (florbetapir F ...

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FDA grants RMAT designation for enGene’s detalimogene, enabling potential for expedited review in high risk, non-muscle invasive bladder cancer

25 June 2025 - enGene Holdings today announced that the US FDA has granted regenerative medicine advanced therapy designation to detalimogene ...

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After 9 year wait, Boehringer’s IPF drug Ofev faces generic threat weeks into Korea launch

24 June 2025 - Just two months after German pharma Boehringer Ingelheim secured long-delayed reimbursement for Ofev in Korea, generics ...

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Novadip receives RMAT designation for NVD003, its regenerative treatment for congenital pseudarthosis of the tibia

23 June 2025 - Novadip Biosciences is developing NVD003, an autologous therapy derived from adipose stem cells, as a potential ...

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Quoin Pharmaceuticals announces FDA grants rare paediatric disease designation for QRX003 in Netherton syndrome

24 June 2025 - Quoin Pharmaceuticals today announced that the US FDA has granted rare paediatric disease designation for the ...

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Linerixibat accepted for review by the EMA for cholestatic pruritus in patients with primary biliary cholangitis

23 June 2025 - Submission based on data from positive GLISTEN Phase 3 trial ...

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Syndax announces FDA priority review of sNDA for Revuforj (revumenib) in relapsed or refractory mNPM1 acute myeloid leukaemia

24 June 2025 - Syndax Pharmaceuticals today announced that the US FDA has granted priority review for its supplemental new drug ...

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FDA approves Benlysta (belimumab) auto-injector for children with active lupus nephritis

24 June 2025 - With this approval, paediatric patients aged five years and older with active lupus nephritis will have ...

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Ozempic receives EU recommendation in peripheral arterial disease, cementing the broad benefits of semaglutide for people with type 2 diabetes and co-morbidities

23 June 2025 - Pending a decision from the European Commission, Ozempic (once weekly semaglutide) will have the broadest approved label ...

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EMA recommends market approval of AVT06, Alvotech’s proposed biosimilar to Eylea (aflibercept)

23 June 2025 - Alvotech and Advanz Pharma today announced that the EMA's CHMP adopted a positive opinion recommending approval for ...

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Revolution Medicines announces FDA breakthrough therapy designation for daraxonrasib in previously treated metastatic pancreatic cancer with KRAS G12 mutations

23 June 2025 - Breakthrough therapy designation based on promising early clinical evidence observed with daraxonrasib in patients with pancreatic ductal ...

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Sarclisa recommended for EU approval by the CHMP to treat transplant-eligible newly diagnosed multiple myeloma

23 June 2025 - Recommendation based on GMMG-HD7 Phase 3 study demonstrating that Sarclisa with bortezomib, lenalidomide, and dexamethasone induction treatment significantly ...

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Australians with cystic fibrosis benefit from life changing expanded listing

24 June 2025 - More Australians living with cystic fibrosis will have affordable access to a life changing treatment option ...

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‘Barriers lifted’: cystic fibrosis treatment reaches final waiting patients

23 June 2025 - Ex-Wallabies player Nathan Charles has lived with cystic fibrosis for decades.  ...

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FDA grants accelerated approval to datopotamab deruxtecan-dlnk for EGFR-mutated non-small cell lung cancer

23 June 2025 - Today, the FDA granted accelerated approval to datopotamab deruxtecan-dlnk (Datroway, Daiichi Sankyo) for adults with locally ...

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