Drug prices on ads: as ‘relevant’ as percent daily value on food labels

9 November 2018 - President Trump announced late last month that his administration will push back on high drug costs ...

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Karyopharm’s selinexor receives fast track designation from FDA for the treatment of patients with relapsed or refractory diffuse large B-cell lymphoma

7 November 2018 - Karyopharm Therapeutics today announced that the U.S. FDA has granted fast track designation to selinexor, the Company’s ...

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Theravance Biopharma and Mylan receive FDA approval for Yuperli (revefenacin) in adults with chronic obstructive pulmonary disease

9 November 2018 - Yuperli (revefenacin) is the first and only once-daily, nebulised bronchodilator approved for the treatment of COPD in ...

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FDA highlights record-breaking number of generic drug approvals in October

9 November 2018 - Today, the U.S. FDA is providing a summary of the generic drug approval actions for the ...

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FDA approves Merck’s Keytruda (pembrolizumab) for the treatment of patients with hepatocellular carcinoma who have been previously treated with sorafenib

10 November 2018 - Approval marks 14th indication for Keytruda. ...

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Lilly snaps up regulatory 'fast pass' for bargain price

2 November 2018 - Priority review vouchers used to be highly sought: back in 2015, for example, AbbVie paid United ...

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Coherus prices biosimilar to Amgen's Neulasta at 33 percent discount

9 November 2018 - Coherus BioSciences Inc said on Thursday it would price its biosimilar to Amgen Inc’s infection-fighting treatment, ...

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Statement from FDA Commissioner on new efforts to strengthen FDA’s expanded access program

8 November 2018 - Since the 1970s, the FDA has helped to facilitate access to promising investigational medical products for ...

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SpringWorks Therapeutics receives FDA fast track designation for nirogacestat for the treatment of adult patients with desmoid tumours

7 November 2018 - SpringWorks Therapeutics today announced that the U.S. FDA has granted fast track designation for nirogacestat, an investigational, ...

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FDA releases real-world data collection app

7 November 2018 - FDA released on Tuesday an open source code app that can be used to collect real-world ...

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Acacia Pharma resubmits Barhemsys new drug application

6 November 2018 - Acacia Pharma announces that it has resubmitted its new drug application for Barhemsys (amisulpride injection) to the ...

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AbbVie announces Humira (adalimumab) global patent license with Momenta

6 November 2018 - AbbVie announced today patent license agreements with Momenta over its proposed biosimilar adalimumab product.  ...

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FDA grants priority review for Dupixent (dupilumab) as potential treatment for adolescents with uncontrolled moderate to severe atopic dermatitis

6 November 2018 - Regeneron Pharmaceuticals and Sanofi today announced that the U.S. FDA has accepted for priority review the ...

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U.S. FDA approves Empliciti (elotuzumab) plus pomalidomide and dexamethasone, a new immunotherapy combination for certain patients with relapsed or refractory multiple myeloma

6 November 2018 - In the ELOQUENT-3 trial, treatment with Empliciti plus pomalidomide and dexamethasone doubled median progression-free survival and overall ...

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FDA approves novel single-vial formulation of Egrifta

5 November 2018 - Theratechnologies is pleased to announce that the FDA in the United States has approved the new ...

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