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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Campaign launched for life-sustaining treatment access across Canada

31 May 2021 - Alpha-1 Canada publicly launched Access for Alphas today, a campaign aimed at raising the awareness of alfa-1 ...

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New Zealand Pharmaceutical Schedule - 1 June 2021 update

1 June 2021 - The June 2021 issue of the New Zealand Pharmaceutical Schedule is now available and in effect. ...

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Suspend intellectual property rights for COVID-19 vaccines

28 May 2021 - Waivers are essential for global vaccine equity ...

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BrainSee novel software is breakthrough for non-invasive detection and monitoring of Alzheimer’s disease at the early stage of mild cognitive impairment

28 May 2021 - Darmiyan’s AI solution reliably guides physicians on prognosis and clinical management of mild cognitive impairment patients. ...

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Eton Pharmaceuticals receives complete response letter from U.S. FDA for dehydrated alcohol injection

28 May 2021 - Eton Pharmaceuticals today announced that the company has received a complete response letter from the U.S. FDA ...

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If the FDA approves Biogen’s Alzheimer’s treatment, I won’t prescribe it

30 May 2021 - Most visits to the memory centre where I care for individuals living with Alzheimer’s disease end ...

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State slower to ‘adopt new drugs’ than most of western Europe

31 May 2021 - Medicines regularly not worth approving at asking price. ...

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FDA grants breakthrough device designation for smart orthopaedic implants

28 May 2021 - Intelligent Implants has announced today that its SmartFuse system has received breakthrough device designation by the ...

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External reference pricing: the drug pricing reform America needs?

27 May 2021 - External reference pricing, sometimes known as international reference pricing, refers to the practice of informing price negotiations ...

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White House asks court to dismiss lawsuit over drug imports

31 May 2021 - The Biden administration is urging a federal court to dismiss a lawsuit that could stand in the ...

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Marketing approval received in Japan for Ninlaro as a maintenance therapy after first-line treatment for multiple myeloma without prior stem cell transplantation

27 May 2021 - Takeda today announced that it has received approval from the Japanese Ministry of Health, Labour and ...

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Examining the impact of different country processes for appraising rare disease treatments: a case study analysis

31 May 2021 - Conventional appraisal and reimbursement processes are being challenged by the increasing number of rare disease treatments with ...

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Apotex medicines in New Zealand

31 May 2021 - Apotex has announced that it is leaving the New Zealand market. ...

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PHARMAC funding will result in health poverty: advocate

30 May 2021 - A Dunedin patient rights campaigner is vowing to fight on in the wake of the Government’s ...

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Diurnal receives European Commission approval for Efmody

28 May 2021 - Commercial launch anticipated in Q3 2021. ...

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