Castle Creek Pharmaceuticals receives FDA fast track designation for diacerein 1% ointment for treatment of epidermolysis bullosa simplex

9 August 2018 - Biopharmaceutical company currently evaluating diacerein 1% ointment in ongoing DELIVERS study. ...

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FDA approves first-of-its kind targeted RNA-based therapy to treat a rare disease

10 August 2018 - The U.S. FDA today approved Onpattro (patisiran) infusion for the treatment of peripheral nerve disease (polyneuropathy) caused ...

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FDA approves new treatment for a rare genetic disorder, Fabry disease

10 August 2018 - The U.S. FDA today approved Galafold (migalastat), the first oral medication for the treatment of adults with ...

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Ironshore Pharmaceuticals announces FDA approval of Jornay PM (methylphenidate) extended-release capsules CII for the treatment of ADHD

9 August 2018 - The commercial launch of Jornay PM is planned for the first half of 2019. ...

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US FDA approves Arakoda (tafenoquine) tablets for oral use; first preventative antimalarial approved in almost two decades

9 August 2018 - 60 Degrees Pharmaceuticals announced today the U.S. FDA approval of Arakoda (tafenoquine) tablets for the prevention of ...

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Americans fund most of the world’s drug research. Here’s how Trump can end that.

9 August 2018 - President Donald Trump recently released an ambitious, 44-page plan to drive down prescription drug prices. The ...

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Sesen Bio announces Vicinium granted fast track designation by FDA for treatment of non-muscle invasive bladder cancer

9 August 2018 - Sesen Bio today announced that the U.S. FDA has granted fast track designation to Vicinium for the ...

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Glenmark Pharmaceuticals announces FDA acceptance of the company's first new drug application for Ryaltris for patients with seasonal allergic rhinitis

7 August 2018 - The PDUFA target action date for completion of the FDA review is 21 March 2019. ...

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Genmab announces submission of U.S. & EU regulatory applications seeking approval of Darzalex (daratumumab) split dosing regimen

8 August 2018 - Applications seek to update prescribing information and summary of product characteristics. ...

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FDA approves treatment for two rare types of non-Hodgkin lymphoma

8 August 2018 - The U.S. FDA today approved Poteligeo (mogamulizumab-kpkc) injection for intravenous use for the treatment of adult patients ...

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FDA approves first generic drug under new pathway aimed at enhancing market competition for sole source drugs

8 August 2018 - The U.S. FDA today approved several strengths of potassium chloride oral solution as the first generic drugs ...

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The FDA is poised to approve the first-ever drug that mutes disease-causing genes

7 August 2018 - After a decades-long wait, the FDA is on the brink of approving a landmark rare disease ...

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Patient reported outcome measures in the FDA pilot compendium: meeting today’s standards for patient engagement in development?

7 August 2018 - In 2016, the FDA released a pilot clinical outcome assessment compendium intended to foster patient-focused drug development.  ...

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Nohla Therapeutics receives FDA fast track designation for dilanubicel for allogeneic cord blood transplant patients

6 August 2018 - Nohla Therapeutics today announced that the U.S. FDA has granted fast track designation to dilanubicel (NLA101) for ...

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Array Biopharma receives FDA breakthrough therapy designation for Braftovi in combination with Mektovi and cetuximab for BRAF V600E mutant metastatic colorectal cancer

7 August 2018 - Designation based on Phase 3 BEACON CRC safety lead-in data. ...

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