Burtomab receives breakthrough therapy designation for advanced form of paediatric cancer

7 June 2017 - Burtomab, a drug for metastatic neuroblastoma, has been granted breakthrough therapy designation by the FDA for the ...

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Cancer drug prices are so high that doctors will test cutting doses

8 June 2017 - A group of prominent cancer doctors is planning a novel assault on high drug costs, using ...

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Novartis’s next challenge: pricing breakthrough cancer treatment

8 June 2017 - Swiss drugmaker mulls linking cost to results in each patient. ...

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Institute for Clinical and Economic Review's final report on treatments for atopic dermatitis provides policy recommendations to support appropriate patient access to dupilumab

8 June 2017 - Report analyses evidence on the comparative effectiveness of dupilumab, finds price well-aligned with added value for patients; ...

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FDA requests removal of Opana ER for risks related to abuse

8 June 2017 - Today, the U.S. FDA requested that Endo Pharmaceuticals remove its opioid pain medication, reformulated Opana ER ...

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Senate health bill may alienate G.O.P. Conservatives

7 May 2017 - Senate Republicans are closing in on a bill to repeal President Barack Obama’s signature health care ...

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Bristol-Myers Squibb announces availability of new Orencia (abatacept) subcutaneous administration option for patients 2 years of age and older with moderately to severely active polyarticular juvenile idiopathic arthritis

8 June 2017 - New pre-filled syringe option can be administered at home. ...

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Major flaws in US drugs with 'accelerated' approval, research suggests

7 June 2017 - A new study published today has exposed major flaws in the fast tracking of some drugs ...

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Biosimilar drugs offer promise for drug price savings, but risks remain

5 June 2017 - The issue of prescription drug prices continues to top the list of public concerns about health ...

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FDA expands approved use of Opdivo to treat lung cancer

4 March 2015 - The U.S. Food and Drug Administration today expanded the approved use of Opdivo (nivolumab) to treat ...

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Bristol-Myers Squibb receives approval from the US FDA for the Opdivo (nivolumab) + Yervoy (ipilimumab) regimen in BRAF V600 wild-type unresectable or metastatic melanoma

30 September 2015 - First and only FDA approved combination of two immuno-oncology agents. ...

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Novartis receives two new FDA approvals for Cosentyx to treat patients with ankylosing spondylitis and psoriatic arthritis in the US

15 January 2016 - FDA approval for Cosentyx is based on efficacy and safety outcomes shown across four Phase III studies, ...

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Mateon Therapeutics receives FDA fast track designation for OXI4503 in patients with acute myeloid leukaemia

7 June 2017 - Mateon Therapeutics today announced that the U.S. FDA has granted fast track designation to the company's product ...

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Calithera Biosciences announces FDA fast track designation granted to CB-839 for treatment of patients with renal cell carcinoma

Calithera Biosciences today announced that the U.S. FDA has granted fast track designation to CB-839 in combination with everolimus, for ...

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Senate GOP aiming to conclude divisive health-care push — one way or the other

6 June 2017 - Senate Republican leaders on Tuesday unveiled a series of policy options to overhaul the nation’s health-care ...

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