FDA approves Praluent (alirocumab) to prevent heart attack, stroke and unstable angina requiring hospitalisation

26 April 2019 - Praluent is the first PCSK9 inhibitor that has shown a meaningful reduction in death from any cause. ...

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FDA approves first treatment for paediatric patients with lupus

26 April 2019 - The U.S. FDA today approved Benlysta (belimumab) intravenous infusion for treatment of children with systemic lupus erythematosus ...

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FDA approves Bausch Health's Duobrii (halobetasol propionate and tazarotene) lotion 0.01%/0.045% for plaque psoriasis in adults

25 April 2019 - First and only topical lotion combining halobetasol propionate and tazarotene in one formulation. ...

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Lilly to establish an access program for patients as it prepares to withdraw Lartruvo from the global market

25 April 2019 - Lilly is working to ensure current patients access to Lartruvo with limited interruption after it is ...

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La Jolla Pharmaceutical announces U.S. FDA’s grant of breakthrough therapy designation for LJPC-0118 for the treatment of severe malaria

24 April 2019 - Designation offers potential for expedited development and review, and highlights the urgent need for additional treatment options ...

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FDA hires Pew director to lead regulatory policy

24 April 2019 - Elizabeth Jungman, a well-known public health expert and a Capitol Hill veteran, will lead the FDA’s ...

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AbbVie expands immunology portfolio in the U.S. with FDA approval of Skyrizi (risankizumab-rzaa) for moderate to severe plaque psoriasis

23 April 2019 - AbbVie today announced that the U.S. FDA approved Skyrizi (risankizumab-rzaa), an interleukin-23 inhibitor, for the treatment of ...

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Pharma lobby nears spending records with drug prices under fire

23 April 2019 - Drug makers, groups disclose first-quarter spending increases. ...

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FDA permits marketing of first medical device for treatment of ADHD

19 April 2019 - The U.S. FDA today permitted marketing of the first medical device to treat attention deficit hyperactivity disorder.  ...

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Intensity Therapeutics receives fast track designation from U.S. FDA for development of INT230-6 as treatment for relapsed or metastatic triple negative breast cancer

17 April 2019 - Intensity Therapeutics today announced that the U.S. FDA has granted fast track designation to the Company’s ...

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FDA approves Merck’s Keytruda (pembrolizumab) in combination with Inlyta (axitinib) as first-line treatment for patients with advanced renal cell carcinoma

22 April 2019 - Approval based on results of KEYNOTE-426, where Keytruda in combination with axitinib reduced the risk of death ...

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US FDA approves Duaklir Pressair (aclidinium/formoterol) for patients with chronic obstructive pulmonary disease

17 April 2019 - Only twice-daily LAMA /LABA in the United States with COPD exacerbation data included in its prescribing information. ...

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Priority review vouchers have helped to improve access to drugs targeting neglected diseases

22 April 2019 - The FDA priority review vouchers for neglected tropical diseases are aimed to incentivise pharmaceutical companies to ...

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U.S. FDA accepts biologics license application for eptinezumab

22 April 2019 - Alder BioPharmaceuticals today announced that the U.S. FDA has accepted for review the biologics license application for ...

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Viela Bio receives U.S. FDA breakthrough therapy designation for inebilizumab for treatment of neuromyelitis optica spectrum disorder

18 April 2019 - Designation based on positive primary analysis of pivotal study, N-MOmentum. ...

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