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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FDA touts success and challenges in biosimilar development

10 November 2021 - A top official from the US FDA offered a mixed assessment of the agency’s biosimilars program, noting ...

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Health tech questions await next FDA chief

10 November 2021 - Twenty months into the pandemic, the FDA remains consumed with vital decisions on coronavirus vaccines and treatments.  ...

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Bolstering our ability to value health technology: a few less considered issues

9 November 2021 - Proposals for a national entity to produce and assess evidence about the relative value of medical technology ...

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Inclusion in health technology assessments: the first step toward equity

10 November 2021 - Many researchers working on health technology assessments are keen to address disparities in health care.  ...

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European Council green lights new rules on health technology assessment, improving access to medicines and simplifying procedures

9 November 2021 - The Council today gave its final go-ahead for the adoption of a regulation on health technology assessment. ...

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Average family premiums for employer-based health insurance have jumped 47% in the last decade, outpacing wage growth and inflation

11 November 2021 - You’re not imagining the growing pinch to your budget from the cost of your workplace health ...

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Patient access to affordable cancer treatment increases with the launch of new biosimilar in Canada

9 November 2021 - Apobiologix today launched its first oncology therapeutic treatment Bambevi (bevacizumab), which is used in combination with ...

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US FDA accepts supplemental new drug application and grants priority review for Jardiance for adults with heart failure independent of left ventricular ejection fraction

11 November 2021 - If approved, Jardiance would be the first clinically proven treatment for adults across the full spectrum ...

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Valneva receives EU deal for COVID jab, and seeks apology from UK

11 November 2021 - French vaccine manufacturer, Valneva, has announced that it has won EU approval to supply up to 60 ...

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COVID-19: EMA recommends authorisation of two monoclonal antibody medicines

11 November 2021 - EMA’s CHMP has recommended authorising Ronapreve (casirivimab/imdevimab) and Regkirona (regdanvimab) for COVID-19. ...

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Moderna booster progress ‘well advanced’ as regulator considers child vaccines

11 November 2021 - Moderna’s coronavirus vaccine could be approved for use as a booster within weeks and the medical ...

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HSE approves reimbursement of Ajovy (fremanezumab) in migraine

11 November 2021 - Teva Pharmaceuticals Ireland has announced the approval of Ajovy (fremanezumab) 225 mg pre-filled syringe for prescription ...

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Tremfya (guselkumab) approved for reimbursement in Ireland for active psoriatic arthritis

11 November 2021 - The Janssen Pharmaceutical Companies of Johnson & Johnson have announced that Tremfya (guselkumab), a first-in-class treatment ...

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COVID-19 vaccine weekly safety report (11 November 2021)

11 November 2021 - To 7 November 2021, the TGA has received 288 reports which have been assessed as likely to ...

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NICE terminates appraisal of new, first in class radioenhancer hafnium oxide nanoparticle

10 November 2021 - NBTXR3 is used to treat patients with sarcoma. ...

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