Sunovion receives FDA approval of supplemental new drug application for use of Latuda (lurasidone hydrochloride) in the treatment of bipolar depression in paediatric patients (10 to 17 years of age)

6 March 2018  - Sunovion Pharmaceuticals today announced that the U.S. FDA approved a supplemental new drug application that expands ...

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FDA approves new HIV treatment for patients who have limited treatment options

6 March 2018 - Today, the U.S. FDA approved Trogarzo (ibalizumab-uiyk), a new type of anti-retroviral medication for adult patients living ...

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Bristol-Myers Squibb’s Opdivo (nivolumab) now the first and only FDA approved PD-1 inhibitor to offer every four week dosing

6 March 2018 - Opdivo also now approved for shorter 30-minute infusions, cutting previous infusion time in half ...

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FDA authorises, with special controls, direct-to-consumer test that reports three mutations in the BRCA breast cancer genes

6 March 2018 - Test only reports 3 out of more than 1,000 known BRCA mutations and negative result doesn’t rule ...

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The Federal Right to Try Act of 2017—a wrong turn for access to investigational drugs and the path forward

6 March 2018 - In 2017, President Trump said that “one thing that’s always disturbed” him is that the US FDA ...

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Jazz Pharmaceuticals announces FDA acceptance of NDA for solriamfetol (JZP-110) for excessive sleepiness associated with narcolepsy or obstructive sleep apnea

2 March 2018 - Jazz Pharmaceuticals today announced that the U.S. FDA has accepted for filing with standard review the company's ...

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Accelerated approval in oncology: FDA touts successes, responds to criticism

5 March 2018 - A majority of oncology treatments granted accelerated approval over the last 25 years have gone on ...

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U.S. FDA accepts new drug application for prucalopride (SHP555) for chronic idiopathic constipation

5 March 2018 - Submission includes real-world evidence from an observational, pharmacoepidemiology cardiovascular safety study. ...

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Otonomy announces FDA approval of Otiprio for acute otitis externa

2 March 2018 - Otonomy today announced that the U.S. FDA has approved Otiprio (ciprofloxacin 6% otic suspension) for the treatment ...

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Biogen and AbbVie announce the voluntary worldwide withdrawal of marketing authorisations for Zinbryta (daclizumab) for relapsing multiple sclerosis

2 March 2018 - Patient safety is the top priority for Biogen and AbbVie. ...

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FDA to review Dupixent (dupilumab) as potential treatment for moderate-to-severe asthma

2 March 2018 - The U.S. FDA has accepted for review the supplemental biologics license application of Dupixent (dupilumab) as an ...

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Under Trump, the pace of FDA regulations slowed to a trickle

28 February 2018 - As the Trump administration settled in last year, the White House insisted on fewer regulations — ...

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FibroGen granted fast track designation by U.S. FDA for pamrevlumab treatment of patients with locally advanced unresectable pancreatic cancer

1 March 2018 - FibroGen today announced that the U.S. FDA has granted fast track designation for the company’s anti-CTGF antibody, ...

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Allergan announces FDA has extended the ulipristal acetate NDA review period to August 2018

1 March 2018 - Allergan today announced that it was notified by the U.S. FDA that the review of the new ...

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Sorrento Therapeutics subsidiary, Scilex, receives US FDA approval for non-opioid ZTlido (lignocaine topical system) 1.8% for PHN pain

28 February 2018 - ZTlido uses novel technology demonstrating 12 hour wear for efficient lignocaine delivery, even during exercise. ...

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