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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MannKind announces US FDA accepts for review its supplemental new drug application of Furoscix ReadyFlow Auto-injector for the treatment of oedema in adults with chronic heart failure or chronic kidney disease

1 December 2025 - MannKind Corporation today announced that the US FDA has accepted the sNDA seeking approval for Furoscix ReadyFlow ...

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GSK’s Jemperli now standard in endometrial cancer as reimbursement expands to first-line therapy

1 December 2025 - GSK’s Jemperli has secured its position as a standard treatment option in endometrial cancer following Korea’s ...

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Solid Biosciences receives FDA rare paediatric disease designation for SGT-212 dual route of administration gene therapy for Friedreich’s ataxia

1 December 2025 - Solid Biosciences today announced that it received rare paediatric disease designation from the US FDA for SGT-212, ...

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Samsung Bioepis announces launch of denosumab biosimilars, Obodence and Xbryk in Europe

1 December 2025 - Samsung Bioepis today announced the launch of Obodence (60 mg pre-filled syringe) and Xbryk (120 mg vial), ...

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Australia’s PBS faces heat from Trump’s new drug pricing deal

2 December 2025 - Britain has agreed to pay 25% more for new medicines to escape Donald Trump’s pharmaceutical tariffs ...

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Health Canada and the FDA collaborate on generic drug information sharing initiative

1 December 2025 - Health Canada's Pharmaceutical Drugs Directorate and the US FDA Office of Generic Drugs have created a program ...

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EMA validates type II variation application for Padcev (enfortumab vedotin) with Keytruda (pembrolizumab) for certain patients with muscle-invasive bladder cancer

1 December 2025 - Astellas Pharma today announced that the EMA validated for review a type II variation application for ...

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Merck granted fast track designation by the US FDA for MK-2214 for the treatment of Alzheimer's disease

1 December 2025 - MK-2214, an investigational novel antibody targeting phosphorylated serine 413 (pS413) tau. ...

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New Zealand Pharmaceutical Schedule - 1 December 2025

1 December 2025 - The December 2025 issue of the New Zealand Pharmaceutical Schedule is now available and in effect. ...

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Ionis receives US FDA breakthrough therapy designation for olezarsen for severe hypertriglyceridaemia

1 December 2025 - On track to submit supplemental new drug application by end of year. ...

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Sound Pharmaceuticals receives FDA breakthrough therapy designation for SPI-1005 to treat Meniere’s disease

1 December 2025 - Sound Pharmaceuticals is pleased to announce that the FDA has granted its investigational new drug, SPI-1005, breakthrough ...

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Cullinan Therapeutics receives FDA fast track designation for CLN-049, a novel FLT3xCD3 T cell engager, in relapsed/refractory acute myeloid leukemia

1 December 2025 - Cullinan Therapeutics today announced that the US FDA has granted fast track designation to CLN-049 for ...

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Vanda Pharmaceuticals provides regulatory update on tradipitant for motion sickness

28 November 2025 - Vanda Pharmaceuticals today announced updates regarding tradipitant for motion sickness. ...

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Lilly lowers the price of Zepbound (tirzepatide) single-dose vials

1 December 2025 - Eli Lilly announced Zepbound (tirzepatide) single dose vials will now be available at lower prices on LillyDirect, ...

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Changes to NICE’s cost effectiveness thresholds confirmed

1 December 2025 - The Government has today announced that it will increase the thresholds NICE uses in evaluations of new ...

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