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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Pfizer and BioNTech announce U.S. FDA approval of their COVID-19 vaccine Comirnaty for adolescents 12 through 15 years of age

8 July 2022 - Approval of the two dose primary series is based on the totality of data through six months ...

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NICE recommends Opdivo as post-surgery treatment

8 July 2021 - The therapy will be used for specific muscle invasive urothelial cancer patients ...

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World’s first chemo drone delivery announced on NHS birthday

5 July 2022 - NHS cancer patients will be the first in the world to benefit from chemotherapy delivered by ...

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Doctors, pharmacists call for better support to prescribe anti-virals

8 July 2022 - Pandemic measures including home delivery of medicines and subsidised Telehealth appointments should be reinstated to allow ...

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US FDA awards rare paediatric disease designation to paxalisib for AT/RT, a rare form of childhood brain cancer

6 July 2022 - Kazia Therapeutics is pleased to announce that the U.S. FDA has awarded rare paediatric disease designation ...

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MSAC updates agenda for July 2022 meeting

7 July 2022 - One application has been added. ...

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Testing for differences in survival when treatment effects are persistent, decaying, or delayed

7 July 2022 - A statistical test for the presence of treatment effects on survival will be based on a null ...

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Vertex announces letter of intent with the pan-Canadian Pharmaceutical Alliance for public reimbursement of Trikafta (elexacaftor/tezacaftor/ivacaftor and ivacaftor) in children with cystic fibrosis ages 6 and older

7 July 2022 - Vertex Pharmaceuticals today announced that it has signed a letter of intent with the pan-Canadian Pharmaceutical ...

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EMA finalises companion diagnostic guidance

7 July 2022 - The EMA) has finalised guidance on companion diagnostics, addressing procedural aspects to facilitate consultation between EMA ...

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PHARMAC keeps medical devices role despite failing to curb costs

8 July 2022 - The government is persisting with a way of buying hugely expensive medical devices that has been proven ...

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Accelerated approval - taking the FDA’s concerns seriously

6 July 2022 - User-fee re-authorisation creates new opportunities for the FDA to address issues with its accelerated-approval program, including the ...

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Expanded eligibility for fourth COVID-19 vaccine dose

7 July 2022 - An additional 7.4 million people will now be eligible to receive a fourth COVID-19 vaccine dose ...

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ATAGI updated recommendations for a winter dose of COVID-19 vaccine

7 July 2022 - ATAGI has updated its recommendations for a winter dose of COVID-19 vaccine to help reduce severe ...

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FDA authorises pharmacists to prescribe Paxlovid with certain limitations

6 July 2022 - New prescribing authority could improve access for some patients at high risk for severe COVID-19. ...

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NICE recommends Janssen’s treatment for active psoriatic arthritis

6 July 2022 - Clinical trial evidence suggests that Tremfya is effective when compared with a placebo ...

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