Department publishes revised agenda for November 2020 PBAC meeting

3 November 2020 - One late change ahead of tomorrow's meeting. ...

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Gilead faces pressure to relinquish valuable FDA voucher awarded with remdesivir approval

2 November 2020 - A prominent advocacy group is asking Gilead Sciences to relinquish a valuable voucher that came with ...

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European Medicines Agency validates marketing application for filgotinib for the treatment of ulcerative colitis

2 November 2020 - Application based on results from pivotal Phase 2b/3 SELECTION trial. ...

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PHARMAC funding resources to focus on medicines access equity

3 November 2020 - PHARMAC is pleased to announce the launch of He Ako Hiringa, a clinical education provider with ...

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Provention Bio completes rolling submission of the biologics license application for teplizumab for the delay or prevention of clinical type 1 diabetes in at risk individuals

2 November 2020 - Submission of chemistry, manufacturing and controls and administrative information modules represent completion of the Company's submission for ...

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European Commission approves Zejula (niraparib) as first-line monotherapy maintenance treatment in advanced ovarian cancer

29 October 2020 - Zejula is the first PARP inhibitor approved as monotherapy in the European Union for patients with platinum-responsive ...

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GSK Nucala (mepolizumab) filings accepted by European Medicines Agency for three additional eosinophil-driven diseases

29 October 2020 - Submissions based on positive data from pivotal studies in hypereosinophilic syndrome, chronic rhinosinusitis with nasal polyps and ...

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PBAC recommends price increase for paracetamol

30 October 2020 - A fascinating insight from the first round of Public Summary Documents from the July 2020 PBAC ...

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Novartis' MONALEESA-7 Kisqali (ribociclib succinate) study demonstrated statistically significant improvement in overall survival in pre- and peri-menopausal women with HR+/HER2- advanced breast cancer

2 November 2020 - Novartis Pharmaceuticals Canada is pleased to announce that statistically significant overall survival  results for Kisqali (ribociclib succinate) ...

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European Commission approves Roche’s Tecentriq in combination with Avastin for the treatment of people with the most common form of liver cancer

2 November 2020 - Tecentriq in combination with Avastin is the first and only cancer immunotherapy regimen approved in Europe for ...

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Janssen submits paliperidone palmitate 6 month supplemental new drug application to U.S. FDA for treatment of schizophrenia in adults

2 November 2020 - If approved, paliperidone palmitate 6 month will be the first and only long-acting injectable schizophrenia treatment with a ...

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NICE talking to you: trends in early HTA engagement

29 October 2020 - In 2009, NICE was one of the first health technology assessment agencies to offer the opportunity ...

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Takeda price hikes for a GI drug may give some patients another kind of stomachache

2 November 2020 - Two weeks ago, Takeda Pharmaceuticals raised the list price of its Entyvio treatment for ulcerative colitis ...

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DBV Technologies announces filing and validation of marketing authorisation application for Viaskin Peanut by European Medicines Agency

2 November 2020 - DBV Technologies today announced that its marketing authorisation application for its investigational product Viaskin Peanut (DBV712) has ...

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On the integration of early health technology assessment in the innovation process: reflections from five stakeholders

28 October 2020 - Early health technology assessment, which includes all methods used to inform industry and other stakeholders about the ...

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