Bausch Health provides update for Duobrii filing

15 February 2019 - Bausch Health announced that the U.S. FDA will be unable to meet today's Prescription Drug User Fee ...

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How much will Americans sacrifice for good health care?

16 February 2019 - A battle is looming over universal health care. Politicians and voters will have to decide whether the ...

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High stakes as Trump, Democrats open drug price talks

16 February 2019 - Democrats and the Trump administration are beginning to hold talks on lowering drug prices as they ...

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Hospital drug prices are up to 7 times greater than Medicare pricing

15 February 2019 - A new study shows something many healthcare patients know all too well: hospitals are charging significant ...

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OncoGenex announces fast track designation granted for custirsen in combination with cabazitaxel/prednisone as second-line chemotherapy in Phase 3 AFFINITY trial of men with metastatic castrate-resistant prostate cancer

 23 April 2014 - Third Phase 3 trial of custirsen to receive FDA fast track designation. ...

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Tokai Pharmaceuticals’ galeterone receives fast track designation from the FDA for the treatment of advanced prostate cancer

12 June 2012 - Tokai Pharmaceuticals today announced that its lead candidate, galeterone (TOK-001), has received fast track designation from ...

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Phase III trial of darolutamide in patients with non-metastatic castration-resistant prostate cancer meets primary endpoint

24 October 2018 - Bayer has been granted fast track designation by the U.S. FDA for darolutamide in men with nmCRPC. ...

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Innocrin Pharmaceuticals granted fast track designation by FDA for VT-464 treatment of patients with metastatic castrate-resistant prostate cancer

6 January 2016 - Seviteronel to be presented in three sessions at the ASCO Genitourinary Cancer Symposium to be held in ...

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FDA grants priority review to Merck’s supplemental biologics license application for Keytruda (pembrolizumab) in combination with Inlyta (axitinib) as first-line treatment for advanced renal cell carcinoma

15 February 2019 - Application based on overall survival and progression-free survival data from Phase 3 KEYNOTE-426 trial. ...

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CymaBay Therapeutics announces seladelpar granted breakthrough therapy designation by the FDA for the treatment of primary biliary cholangitis

15 February 2019 - CymaBay Therapeutics today announced that the U.S. FDA has granted breakthrough therapy designation for seladelpar for ...

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ICER publishes final new evidence update for alirocumab, a PCSK9 inhibitor for treating high cholesterol

15 February 2019 - Based on new analyses of published results of the ODYSSEY Outcomes trial, alirocumab would meet cost-effectiveness thresholds ...

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FDA advances new efforts to promote development of safe and effective regenerative medicine products

15 February 2019 - Today, the FDA finalised two guidance documents regarding regenerative medicine therapies.  ...

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Statement from FDA Commissioner on new policy to improve access and foster price competition for drugs that face inadequate generic competition

15 February 2019 - In too many cases, branded drugs that are no longer protected by patents or other exclusivities ...

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CMS proposes coverage with evidence development for chimeric antigen receptor (CAR) T-cell therapy

15 February 2019 - Proposed decision would provide nationwide consistency in CMS’s coverage of the innovative new cancer therapy, to ...

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RDD Pharma receives fast track designation from FDA for RDD-0315 for treatment of faecal incontinence in spinal cord injury patients

14 February 2019 - RDD Pharma announced today that the U.S. FDA granted fast track status for RDD-0315 for the treatment ...

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