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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Health Minister ‘committed’ to listing weight loss drugs on PBS

9 January 2026 - ‘It’s an equity issue as well as a health issue from my perspective.’ ...

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Aquestive Therapeutics announces regulatory development for Anaphylm (dibutepinephrine) sublingual film

9 January 2026 - Announces receipt of FDA letter stating it has identified deficiencies that preclude labeling discussions for Anaphylm at ...

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Camurus announces FDA acceptance of NDA resubmission for Oclaiz for the treatment of acromegaly

9 January 2026 - Camurus today announced that the US FDA has accepted for review the company's resubmission of the new ...

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Stimulant meds for ADHD now fastest growing drug on PBS

11 January 2026 - A stimulant drug used to treat ADHD has become the fastest-growing script on the PBS, prompting ...

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Agenda for the March 2026 PBAC meeting (9 January 2026)

9 January 2026 - The Department of Health has published an updated agenda for the March 2026 PBAC agenda (version ...

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GSK’s Shingrix (recombinant zoster vaccine) pre-filled syringe presentation approved by the European Commission

7 January 2026 - New presentation will begin rolling out across EU countries in 2026. ...

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Wockhardt files marketing authorisation application for WCK 5222 with EMA

7 January 2026 - Wockhardt has successfully filed a marketing authorisation application with the EMA for its novel antibiotic, WCK ...

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Annexon submits tanruprubart marketing authorisation application to the EMA for Guillain-Barré syndrome

8 January 2026 - BLA submission with US/European data from FORWARD trial planned in 2026 ...

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VectorY Therapeutics receives FDA fast track designation for VTx-002, a first in class vectorised antibody targeting underlying disease biology in ALS

8 January 2026 - VectorY Therapeutics announced today that the US FDA has granted fast track designation for VTx-002, a first-in-class ...

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Revolution Medicines announces FDA breakthrough therapy designation for zoldonrasib

8 January 2026 - First breakthrough therapy designation for an investigational drug specifically targeting KRAS G12D mutation in non-small cell lung ...

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858 Therapeutics announces FDA fast track designation for PARG inhibitor ETX-19477 for the treatment of patients with BRCA mutated, platinum resistant ovarian cancer

8 January 2026 - 858 Therapeutics today announced that the US FDA has granted fast track designation to ETX-19477, the company’s ...

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Alessa Therapeutics announces FDA fast track designation for Enolen, a first of its kind treatment for localised prostate cancer

8 January 2026 - Alessa Therapeutics today announced that the US FDA has granted fast track designation for Enolen, the ...

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Complement Therapeutics announces FDA fast track designation for CTx001 for the treatment of geographic atrophy secondary to AMD

8 January 2025 - Complement Therapeutics today announced that the US FDA has granted fast track designation for CTx001, the company's ...

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Vanda Pharmaceuticals announces receipt of FDA decision letter on Hetlioz supplemental new drug application for jet lag disorder

8 January 2026 - Vanda Pharmaceuticals today announced that it has received a decision letter from the US FDA's Center for ...

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Cheaper medicines for children's inflammatory diseases, rare liver disease and multiple sclerosis

8 January 2026 - Australians living with a range of debilitating conditions including juvenile arthritis, rare liver disease and multiple ...

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