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 economic assessment of Trodelvy in advanced triple negative breast cancer

23 May 2022 - TLV has produced a health economic assessment for the regions for the drug Trodelvy (sacituzumab govitecan).  ...

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'Intensive work' ongoing to give 35 children with cystic fibrosis access to life-changing drug

24 May 2022 - Health Minister Stephen Donnelly has said he wants to see the 35 children with cystic fibrosis ...

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Elevation Oncology announces FDA fast track designation granted to seribantumab for the tumour agnostic treatment of solid tumours harbouring NRG1 gene fusions

25 May 2022 - Elevation Oncology today announced that the U.S. FDA has granted fast track designation to seribantumab for the ...

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Servier announces FDA approval of Tibsovo (ivosidenib tablets) in combination with azacitidine for patients with newly diagnosed IDH1 mutated acute myeloid leukaemia

25 May 2022 - FDA approval based on data from the global, Phase 3 AGILE trial that demonstrated a statistically ...

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New injectable immunotherapy treatment for rare form of triple negative breast cancer recommended by NICE

25 May 2022 - An estimated 100 people per year with triple negative breast cancer that has spread to other ...

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Remake of National Health (Supply of Pharmaceutical Benefits – Under Co-payment Data and Claims for Payment) Rules 2022

25 May 2022 - The Department has recently remade the National Health (Claims and under co-payment data) Rules 2012, now ...

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Bausch + Lomb receives Health Canada approval of Lumify redness reliever eye drops

24 May 2022 - Lumify is Canada's first and only over the counter eye drop with low dose brimonidine for ...

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Expanded ATAGI recommendations on winter COVID-19 booster doses for people at increased risk of severe COVID-19

25 May 2022 - The Australian Technical Advisory Group on Immunisation (ATAGI) have expanded their recommendations on the use of additional ...

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Review of discount rate in the PBAC Guidelines

25 May 2022 - The Commonwealth has entered into a new Strategic Agreement in relation to reimbursement, health technology assessment ...

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Verrica receives complete response letter from the FDA for its NDA for VP-102

24 May 2022 - Verrica has been advised that pre-approval inspection was conducted at Sterling and is not aware of any ...

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Kiwis with cystic fibrosis feel forced to move overseas for affordable treatment

25 May 2022 - More Kiwis with cystic fibrosis are moving abroad for treatment, knowing they will die sooner if ...

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Blue Lake Biotechnology announces FDA fast track designation for BLB-201 intranasal RSV vaccine

24 May 2022 - Blue Lake Biotechnology today announced that the U.S. FDA has granted fast track designation for BLB-201, an ...

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NICE doesn’t recommend ibrutinib for those with Waldenstrom’s macroglobulinaemia

23 May 2022 - Ibrutinib, a drug used to treat Waldenström’s macroglobulinaemia, is not being recommended by NICE in England ...

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HLS Therapeutics obtains public reimbursement for Vascepa in Quebec

24 May 2022 - Quebec becomes the first province to reimburse Vascepa for the reduction of cardiovascular risk in patients with ...

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Thousands of people in England could benefit after NICE recommends treatment option for two forms of sight loss

24 May 2022 - NICE recommends faricimab as treatment option for adults with wet age-related macular degeneration or diabetic macular oedema. ...

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