Amgen submits regulatory applications for Repatha (evolocumab) cardiovascular outcomes data in US and Europe

 5 June 2017 - Amgen today announced the submission of a supplemental biologics license application to the U.S. FDA and a ...

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FDA expands use of Sapien 3 artificial heart valve for high-risk patients

5 June 2017 - Expanded use approval relies on real world evidence. ...

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Outcry over EpiPen prices hasn’t made them lower

4 June 2017 - A few weeks ago, after some particularly incompetent parenting on my part (nuts in the dessert, ...

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Moving in the wrong direction — health care under the AHCA

31 May 2017 - On May 4, the U.S. House of Representatives resurrected Republican efforts to enact major health care legislation ...

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The first hundred days for health care

31 May 2017 - Like my predictions about what a Republican win in the 2016 election would mean for U.S. health ...

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The specialists’ stranglehold on medicine

3 June 2017 - Republicans are trying to cut health care spending. But hacking away at Medicaid, weakening coverage requirements ...

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The doctor is in. Co-pay? $40,000.

3 June 2017 - When John Battelle’s teenage son broke his leg at a suburban soccer game, naturally the first ...

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Obama unwittingly handed Trump a weapon to cripple the health law

3 June 2017 - Obama administration officials knew they were on shaky ground in spending billions of dollars on health ...

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The single payer party? Democrats shift left on health care

3 June 2017 - For years, Republicans savaged Democrats for supporting the Affordable Care Act, branding the law — with ...

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Measuring value and benefit—a matter of perspective

2 June 2017 - There is growing concern about the sustainability of health-care systems as the populations of high-income countries age ...

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ViiV Healthcare submits regulatory applications for the first HIV maintenance regimen comprising only two medicines

1 June 2017 - Priority review voucher submitted in US with anticipated target action date of 6 months. ...

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Merck receives accelerated approval of Keytruda (pembrolizumab), the first FDA approved anti-PD-1 therapy

4 September 2014 - Merck today announced that the US FDA has approved Keytruda (pembrolizumab) at a dose of 2 ...

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FDA approves expanded indication for Merck’s Keytruda (pembrolizumab) for the treatment of patients with advanced melanoma

18 December 2015 - Keytruda is now the first and only anti-PD-1 therapy to achieve superior overall survival compared to ipilimumab. ...

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FDA approves Merck’s Keytruda (pembrolizumab) for patients with recurrent or metastatic head and neck squamous cell carcinoma with disease progression on or after platinum-containing chemotherapy

5 August 2016 - Merck today announced that the U.S. FDA has approved Keytruda (pembrolizumab), the company’s anti-PD-1 (programmed death ...

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Pfizer hikes U.S. prices of 91 drugs by average 20% in 2017

2 June 2017 - Pfizer  has hiked the price of nearly a hundred drugs by an average of 20% so ...

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