Evusheld long-acting antibody combination recommended for approval in the EU for the treatment of COVID-19

16 September 2022 - Recommendation based on TACKLE Phase 3 treatment data showing reduced risk of severe COVID-19 or death. ...

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PHARMAC can't progress cystic fibrosis drug Trikafta - CF New Zealand

16 September 2022 - PHARMAC is not in a position to progress funding on the life-extending cystic fibrosis drug, Trikafta, ...

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B.C. family grateful for expanded funding to cystic fibrosis drug, but questions why it took so long

7 September 2022 - B.C. is last Canadian jurisdiction to fund Trikafta for patients with cystic fibrosis age 6 to 11. ...

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Vertex announces U.S. FDA approval for Orkambi (lumacaftor/ivacaftor) in children with cystic fibrosis ages 12 to <24 months

2 September 2022 - With this approval, approximately 300 children with two copies of the F508del mutation will have a ...

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Azurity Pharmaceuticals announces FDA approval of Konvomep (omeprazole and sodium bicarbonate for oral suspension)

2 September 2022 - Azurity Pharmaceuticals announced today that the US FDA has approved Konvomep (omeprazole and sodium bicarbonate for oral ...

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Amneal announces submission of new drug application to the US FDA for IPX203 for the treatment of Parkinson’s disease

31 August 2022 - IPX203 is a novel, extended-release oral formulation of carbidopa and levodopa that if approved, would offer patients ...

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Evusheld long-acting antibody combination approved for prevention and treatment of COVID-19 in Japan

30 August 2022 - First global approval for Evusheld as a COVID-19 treatment. ...

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Access criteria for new COVID-19 treatment announced

25 August 2022 - PHARMAC has today confirmed the access criteria for the first preventative medicine for COVID-19, tixagevimab and cilgavimab ...

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European Medicines Agency commences review of oral fixed-dose combination of decitabine and cedazuridine for the treatment of adults with acute myeloid leukaemia

22 August 2022 - Otsuka and Astex Pharmaceuticals today announce that the EMA has accepted the marketing authorisation application for the ...

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Axsome Therapeutics announces FDA approval of Auvelity, the first and only oral NMDA receptor antagonist for the treatment of major depressive disorder in adults

19 August 2022 - Auvelity is the first and only rapid-acting oral treatment approved with labelling of statistically significant improvement in ...

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Chiesi’s Trimbow recommended for use within NHS Scotland

18 August 2022 - The SMC approval brings much needed boost to asthma sufferers across Scotland. ...

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PHARMAC estimates Trikafta could give people with CF another 27 years

17 August 2022 - PHARMAC has today published the record of advice from the May PTAC meeting to again consider ...

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Myovant Sciences and Pfizer receive U.S. FDA approval of Myfembree, a once daily treatment for the management of moderate to severe pain associated with endometriosis

5 August 2022 - Data from the Phase 3 SPIRIT program showed Myfembree reduced menstrual pain and non-menstrual pelvic pain in ...

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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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Accuretic users annoyed over contaminated blood pressure medication muddle

4 July 2022 - Confusion continues as Kiwis learn months after the rest of the world that widely used blood ...

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