PBS listing of Paxlovid (nirmatrelvir and ritonavir)

 9 April 2022 - Commencing 1 May 2022, Paxlovid (nirmatrelvir and ritonavir) will be listed on the PBS as a General ...

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PBAC recommendation for nirmatrelvir and ritonavir (Paxlovid) - March 2022

9 April 2022 - The PBAC undertook an expedited consideration of a submission to add the combination product, nirmatrelvir and ritonavir ...

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Public Summary Documents – December 2021 PBAC meeting

1 April 2022 - The Public Summary Documents (positive recommendations and subsequent decisions not to recommend) from the December 2021 PBAC ...

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Funding Trikafta for Kiwis with cystic fibrosis - setting the record straight

31 March 2022 - On Monday 28 March, Carmen Shanks presented her Parliamentary Petition to MP Shanan Halbert, urging the ...

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Schedule of Pharmaceutical Benefits - 1 April 2022

1 April 2022 - The April 2022 issue of the Schedule of Pharmaceutical Benefits is out and now in effect. ...

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ViiV Healthcare announces US FDA approval of Triumeq PD, the first dispersible single tablet regimen containing dolutegravir, a once-daily treatment for children living with HIV

30 March 2022 - The FDA approval of the first dispersible single tablet regimen containing dolutegravir increases age-appropriate treatment options ...

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Cystic fibrosis: early access granted to the Kaftrio/Kalydeco combination

29 March 2022 - The High Authority for Health has authorised early access to a first treatment for children aged 6 ...

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Te Pāti Māori demand accountability from PHARMAC CE for lie about live saving Trikafta drug cost

28 March 2022 - Today Te Pāti Māori stand in solidarity with the cystic fibrosis community of Aotearoa New Zealand ...

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Landmark PBS listing for Australians with cystic fibrosis

27 March 2022 - From April 1 2022, Trikafta (elexacaftor with tezacaftor and ivacaftor and ivacaftor) will be available on ...

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Evusheld long-acting antibody combination recommended for approval in the EU for the pre-exposure prophylaxis of COVID-19

24 March 2022 - Recommendation based on Phase 3 PROVENT trial showing a significant reduction in the risk of developing ...

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U.S. Food and Drug Administration approves first LAG-3 blocking antibody combination, Opdualag (nivolumab and relatlimab-rmbw), as treatment for patients with unresectable or metastatic melanoma

18 March 2022 - Opdualag is a first in class, fixed-dose dual immunotherapy combination treatment of the PD-1 inhibitor nivolumab and ...

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Heron Therapeutics announces approval of Zynrelef by Health Canada for the management of post-operative pain

17 March 2022 - ZYNRELEF is the first and only extended-release local anaesthetic approved by Health Canada. ...

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FDA approves first generic of Symbicort to treat asthma and COPD

15 March 2022 - Agency supports development of complex generic drug-device combination product to improve competition and access to more affordable ...

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Amylyx Pharmaceuticals announces EMA validation of marketing authorisation application for AMX0035 for the treatment of ALS

25 February 2022 - Amylyx Pharmaceuticals today announced that its marketing authorisation application to the EMA CHMP for AMX0035 (sodium phenylbutyrate ...

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Cystic fibrosis community disappointed with PTAC recommendations

23 February 2022 - New Zealand’s cystic fibrosis community received disappointing news today with a recommendation to PHARMAC that reduces ...

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