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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U.S. probes how pharmacies set drug prices as costs rise

7 June 2022 - The U.S. Federal Trade Commission has opened a probe into how big pharmacy benefit managers like ...

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AARP continues fight for lower prescription drug prices

7 June 2022 - Older Americans shouldn’t have to choose between their medication and rent or groceries. ...

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Response to engagement on proposals for the Innovative Medicines Fund

7 June 2022 - NHS England and NICE asked for comments on our proposals for the Innovative Medicines Fund.  ...

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Patients to have earlier access to cutting edge treatments on NHS

7 June 2022 - The most promising medicines will be fast-tracked to NHS patients through Innovative Medicines Fund ...

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Sifi announces EMA validation of its marketing authorisation application for Akantior for the treatment of acanthamoeba keratitis

7 June 2022 - Sifi has launched an early access program across European countries in June 2022. ...

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The online Pharmaceutical Schedule gets a refresh

7 June 2022 - PHARMAC's online Pharmaceutical Schedule has had a refresh with new features to improve the user experience.  ...

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COVID mRNA vaccines can be quickly updated for new variants. So, where's my Omicron booster?

6 June 2022 - Since Omicron was declared a variant of concern at the end of November, it quickly swept ...

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BioCryst announces Health Canada has authorised Orladeyo (berotralstat), the only oral treatment for the prevention of hereditary angioedema attacks

6 June 2022 - BioCryst Pharmaceuticals today announced that Health Canada has approved oral, once daily Orladeyo (berotralstat) for the ...

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Medigen applies for Australian vaccine approval

7 June 2022 - Medigen Vaccine Biologics has applied to the Australian medicines regulator for provisional approval of its COVID-19 ...

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Novavax faces high stakes FDA review this week that will decide the fate of its COVID vaccine in the U.S.

6 June 2022 - If they endorse the vaccine, the FDA will almost certainly authorise the shot for adults in the ...

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Bristol Myers Squibb withdraws supplemental biologics license application for Reblozyl (luspatercept-aamt) for non-transfusion dependent beta thalassaemia

3 June 2022 - Bristol Myers Squibb today announced that the company has withdrawn a supplemental biologics license application for ...

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GBT’s inclacumab and GBT601 receive U.S. FDA orphan drug and rare paediatric disease designations for the treatment of sickle cell disease

6 June 2022 - Inclacumab is a novel P selectin inhibitor currently in Phase 3 clinical trials to reduce vaso-occlusive ...

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FDA approves Riabni (rituximab-arrx), a biosimilar to Rituxan (rituximab), for adults with moderate to severe rheumatoid arthritis

6 June 2022 - Now approved to treat all available Rituxan Indications. ...

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GSK announces US FDA approval of Priorix for the prevention of measles, mumps and rubella in individuals 12 months of age and older

6 June 2022 - Priorix becomes an additional source of measles, mumps and rubella vaccine for US patients ...

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Values, principles, strategies, and frameworks underlying patient and public involvement in health technology assessment and guideline development: a scoping review

3 June 2022 - The importance of patient and public involvement is recognised by agencies involved in health technology assessment and ...

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