If the shutdown drags on at FDA, it will put anticipated new treatments in jeopardy

14 January 2019 - The government shutdown could soon jeopardise highly anticipated new drugs from Janssen, Sanofi, and Novartis for ...

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How a 'regulatory dead zone' may be holding up copycat insulin

14 January 2019 - The insulin market has increasingly attracted scrutiny from politicians, regulators and patient groups, as prices ramp ...

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Statement from FDA Commissioner and Director of the Center for Biologics Evaluation and Research on new policies to advance development of safe and effective cell and gene therapies

15 January 2019 - The FDA is witnessing a surge of cell and gene therapy products entering early development, evidenced ...

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FDA approves expanded use of Adacel (Tdap) vaccine for repeat vaccination

14 January 2019 - First and only vaccine approved in the U.S. for repeat vaccination 8 years or more after the ...

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Exelixis announces U.S. FDA approval of Cabometyx (cabozantinib) tablets for previously treated hepatocellular carcinoma

14 January 2019 - Approval based on statistically significant and clinically meaningful overall survival benefit demonstrated in the CELESTIAL phase 3 ...

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Samsung faces resistance from big pharma in the U.S.

11 January 2019 - Incumbent biologic drug makers use rebates and exclusive contracts to fend off competition from new entrants. ...

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US FDA accepts regulatory submissions for review of tafamidis to treat transthyretin amyloid cardiomyopathy

14 January 2019 - FDA grants a priority review based on Phase 3 ATTR-ACT study findings. ...

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Why pharmaceutical companies are on a shopping binge

14 January 2019 - With the cost of R&D so high, it may make sense to spend money on a competitor. ...

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A revolutionary drug that could treat a rare and devastating disease is prohibitively expensive. But one state has a plan to pay for its potential $5 million price tag.

13 January 2019 - A one-time treatment for a devastating rare disease could be paid for with an instalment plan as ...

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Ocular Therapeutix submits supplemental new drug application for Dextenza (dexamethasone ophthalmic insert) for the treatment of ocular inflammation following ophthalmic surgery

10 January 2019 - Application expands the current Dextenza post-operative pain label as the first intra-canalicular insert for drug delivery. ...

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US FDA sets PDUFA date for Scenesse

10 January 2019 - FDA does not plan to hold advisory committee meeting. ...

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Partial government shutdown's impact on FDA drug approvals

10 January 2019 - As the partial federal government shutdown drags on into its third week, its impact is being felt ...

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FDA approves 59 novel drugs in 2018

8 January 2019 - The past year proved to be a big one for the U.S. FDA and the approval ...

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OncoNano receives authorisation to proceed from FDA for IND application and fast track designation for ONM-100, intra-operative imaging agent to detect tumours and metastatic lymph nodes that often go undetected during surgery

4 January 2019 - FDA says proposed Phase 2 clinical trial may proceed. ...

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RadioMedix and Curium announce FDA fast track designation for 64Cu dotatate

9 January 2019 - RadioMedix and its commercial partner Curium announced today that their investigational diagnostic radiopharmaceutical, 64Cu dotatate, was granted ...

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