Selumetinib granted US breakthrough therapy designation in neurofibromatosis type 1

1 April 2019 - Selumetinib is a MEK 1/2 inhibitor being co-developed by AstraZeneca and MSD. ...

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Circassia announces FDA approval of Tudorza supplemental new drug application

29 March 2019 - Data showing reduction in COPD exacerbations and no increase in major cardiovascular events vs placebo added to ...

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U.S. FDA acknowledges receipt of Intellipharmaceutics' resubmission of oxycodone ER new drug application, deems it a complete response, and designates 28 August 2019 as goal date for review

29 March 2019 - Intellipharmaceutics announced today that the U.S. FDA has acknowledged receipt of its resubmission of the Oxycodone ER ...

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Bernie Sanders vows to cut prescription drug prices by half if he's elected

31 March 2019 - Independent Sen. Bernie Sanders of Vermont, one the leading contenders for the Democratic presidential nomination, pledged ...

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Statement by FDA Commissioner, Director of FDA’s Center for Drug Evaluation and Research and Director of FDA’s Center for Biologics Evaluation and Research on expanded access–looking forward

29 March 2019 - For more than 30 years, the FDA has supported patients’ access to investigational medical products for ...

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Spero Therapeutics receives FDA fast track designation for SPR994 for the treatment of complicated urinary tract infections and acute pyelonephritis

29 March 2019 - Spero Therapeutics today announced that the U.S. FDA granted fast track designation for SPR994, Spero’s lead product ...

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FDA approves new oral treatment for multiple sclerosis

29 March 2019 - The U.S. FDA today approved Mavenclad (cladribine) tablets to treat relapsing forms of multiple sclerosis (MS) ...

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Janssen submits supplemental new drug application to U.S. FDA for Invokana (canagliflozin) for the treatment of chronic kidney disease in patients with type 2 diabetes mellitus

28 March 2019 - Submission is based on data from the landmark Phase 3 CREDENCE renal outcomes study, which stopped early ...

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Amarin submits supplemental new drug application to U.S. FDA seeking new indication for Vascepa (icosapent ethyl) to reduce the risk of major adverse cardiovascular events based on landmark REDUCE-IT cardiovascular outcomes study

28 March 2019 - Amarin Corporation today announced that, as planned, it submitted a supplemental new drug application to the U.S. ...

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Single-payer drug pricing in a multi-payer health system: does Germany offer a model for the US?

22 March 2019 - An increasing number of presidential hopefuls, most recently Senator Kamala Harris, are proposing “single payer” or “Medicare ...

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Hospital pharmacists face dozens of drug shortages yearly

28 March 2019 - More than two-thirds of pharmacists in U.S. hospitals deal with at least 50 drug shortages every year, ...

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Coalition attacks Trump plan to end drug rebates, calling it a ‘big pharma bailout’

28 March 2019 - A coalition that includes pharmacy middlemen and insurers has launched a six-figure ad campaign attacking a ...

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Why J&J raced to put drug prices in some TV ads

28 March 2019 - One notion proposed by the Trump administration to blunt the rising cost of medicines is to ...

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Drug makers continue to clamour for FDA approval of orphan drugs

28 March 2019 - Orphan drugs may serve small groups of patients, but they generate big numbers at the Food ...

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FDA approves treatment for patients with a type of inflammatory arthritis

28 March 2019 - The U.S. FDA today approved Cimzia (certolizumab pegol) injection for treatment of adults with a certain type ...

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