Rising prices of targeted oral anti-cancer medications and associated financial burden on Medicare beneficiaries

1 August 2017 - The high cost of oncology drugs threatens the affordability of cancer care.  ...

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Republicans in Congress bypass Trump to shore up health law

1 August 2017 - Congressional Republicans moved on Tuesday to defuse President Trump’s threat to cut off critical payments to ...

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FDA approves Kalydeco (ivacaftor) for more than 600 people ages 2 and older with cystic fibrosis who have certain residual function mutations

1 August 2017 -  Vertex Pharmaceuticals today announced that the U.S. Food and Drug Administration (FDA) has approved Kalydeco (ivacaftor) ...

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AiCuris granted fast track designation by U.S. FDA for oral pritelivir for treatment of HSV infections in immunocompromised adults

1 August 2017 - AiCuris today announced that the Company has been granted fast track designation by the U.S. FDA ...

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The Americans who saved health insurance

1 August 2017 - Many Americans look back on the heroic political fights of the past — for suffrage, Social ...

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Express Scripts will exclude more drugs next year, limiting patient choice to save health plans millions

31 July 2017 - Express Scripts, the nation’s largest pharmacy benefits manager, will exclude an additional 64 medicines next year ...

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Sanders to unveil rule requiring drug companies to set fair prices

31 July 2017 - Senator Bernie Sanders will unveil a new rule forcing pharmaceutical companies to set reasonable prices for ...

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FDA approves new targeted treatment for relapsed or refractory acute myeloid leukaemia

1 August 2017 - The U.S. FDA today approved Idhifa (enasidenib) for the treatment of adult patients with relapsed or refractory ...

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Bristol-Myers Squibb receives FDA approval for Opdivo (nivolumab) in MSI-H or dMMR metastatic colorectal cancer that has progressed following treatment with a fluoropyrimidine, oxaliplatin, and irinotecan

1 August 2017 - Approval based on CheckMate -142, in which Opdivo demonstrated an objective response rate of 28% (95% CI: ...

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Indivior RBP-6000 NDA acceptance with priority review designation

31 July 2017 - FDA sets a PDUFA target action date of 30 November 2017. ...

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Kite files the industry's first CAR-T marketing authorisation application in Europe for axicabtagene ciloleucel

31 August 2017 - Submission based on primary analysis of ZUMA-1 in patients with aggressive NHL. ...

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Acalabrutinib granted breakthrough therapy designation by US FDA for the treatment of patients with mantle cell lymphoma

1 August 2017 - AstraZeneca and its haematology research and development centre of excellence, Acerta Pharma, today announced that the US ...

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New system speeds FDA import decisions

31 July 2017 - The data is in. A new automated system for determining whether FDA regulated products can enter the ...

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Imfinzi granted breakthrough therapy designation by US FDA for patients with locally-advanced unresectable non-small-cell lung cancer

31 July 2017 - Fourth breakthrough therapy designation for an AstraZeneca new oncology medicine in three years. ...

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Express Scripts to cover Mylan's EpiPen, exclude rivals

1 August 2017 - Pharmacy benefit manager Express Scripts Holding Co said on Monday it would favour drugmaker Mylan Inc's ...

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