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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ITM announces FDA acceptance of new drug application and PDUFA date for lutetium Lu 177 edotreotide (ITM-11) in gastro-enteropancreatic neuroendocrine tumours

13 November 2025 - 2025 - ITM Isotope Technologies today announced that the US FDA completed its filing review and accepted ...

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Allterum Therapeutics receives FDA fast track designation for 4A10 in acute lymphoblastic leukaemia

11 November 2025 - Allterum Therapeutics today announced that the US FDA has granted fast track designation for its lead program, ...

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PHARMAC to fund alternative treatment for tooth decay

12 November 2025 - PHARMAC will fund silver diamine fluoride for the treatment and prevention of tooth decay from 1 December ...

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FDA approves Promega OncoMate MSI Dx analysis system as companion diagnostic for Keytruda in combination with Lenvima in advanced endometrial carcinoma

11 November 2025 - The US FDA has approved the Promega OncoMate MSI Dx Analysis System as a companion diagnostic designed ...

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FDA approves new interchangeable biosimilar to Perjeta

13 November 2025 - Today, the FDA approved Poherdy (pertuzumab-dpzb, Shanghai Henlius Biologics) as an interchangeable biosimilar to Perjeta (pertuzumab, ...

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FDA approves ziftomenib for relapsed or refractory acute myeloid leukaemia with a NPM1 mutation

13 November 2025 - Today, the FDA approved ziftomenib (Komzifti, Kura Oncology), a menin inhibitor, for adults with relapsed or ...

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Marius Pharmaceuticals expands global footprint with Health Canada approval of Kyzatrex (testosterone undecanoate) CIII capsules

12 November 2025 - Marius Pharmaceuticals today announced that Health Canada has approved Kyzatrex (testosterone undecanoate) CIII capsules.  ...

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Cheaper cancer and chronic conditions medicines now on PBS

13 November 2025 - Australians living with cancer and chronic conditions will now have access to life-changing medicine thanks to ...

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Parabilis Medicines receives FDA fast track designation for FOG-001, the first and only direct inhibitor of the β-catenin:TCF interaction for the treatment of desmoid tumours

12 November 2025 - Parabilis Medicines today announced that the US FDA has granted fast track product designation to FOG-001 ...

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Artios receives US FDA fast track designation for alnodesertib in ATM negative metastatic colorectal cancer

24 September 2025 - Artios Pharma today announced that the US FDA granted fast track designation to its ATR inhibitor, ...

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SMC - November 2025 decisions

10 November 2025 - The SMC, which advises on newly licensed medicines for use by NHSScotland, has today published advice ...

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PHARMAC to fund five medicines for multiple sclerosis, breast cancer, eye conditions, and lung cancer

12 November 2025 - New Zealanders living with multiple sclerosis, breast cancer, eye conditions, and lung cancer will benefit from ...

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AstraZeneca’s Imfinzi, Imjudo, and Ultomiris clear reimbursement panel review

7 November 2025 - AstraZeneca's anti-PD-L1 immune checkpoint inhibitor Imfinzi (durvalumab), the anti-CTLA-4 immune checkpoint inhibitor Imjudo (tremelimumab), and the ...

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March Biosciences receives FDA regenerative medicine advanced therapy designation for MB-105 in relapsed/refractory CD5 positive T-cell lymphoma

11 March 2025 - March Biosciences today announced that the US FDA has granted regenerative medicine advanced therapy designation to ...

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EMA publishes agenda for 10-13 November 2025 CHMP meeting

10 November 2025 - The EMA has published a draft agenda for this week's CHMP meeting. ...

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