More Government regulation of biopharma would harm patients and the economy

8 March 2022 - The United States leads the world in creating the new drugs and vaccines that cure or control ...

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7 Hills Pharma’s clinical stage novel immunostimulant 7HP349 granted FDA fast track designation for anti-PD-1 resistant metastatic melanoma

8 March 2022 - 7 Hills Pharma announced today that the U.S. FDA has granted fast track designation to 7HP349, 7HP’s ...

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Saluda Medical receives FDA approval for the Evoke spinal cord stimulation system to treat chronic intractable pain

8 March 2022 - Evoke system deemed superior to open loop spinal cord stimulation in treating overall back and leg pain. ...

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FDA effort to improve clinical trial diversity failed to make a difference for Black patients, study finds

7 March 2022 - Six years ago, the U.S. FDA launched a five year action plan to improve the diversity and ...

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FDA offers funding for biosimilar regulatory science pilot

7 March 2022 - The US FDA is offering funding for several research proposals under the regulatory science pilot for ...

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Merit Medical receives FDA breakthrough device designation for Embosphere microspheres for use in genicular artery embolisation for symptomatic knee osteoarthritis

7 March 2022 - Merit Medical Systems announced today that it has received breakthrough device designation from the U.S. FDA ...

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Key Democrat moves to crack down on FDA accelerated approvals

7 March 2022 - A powerful Democratic lawmaker has introduced a bill that would dramatically rein in the Food and ...

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Teva announces launch of a first generic version of Revlimid (lenalidomide capsules) in the U.S.

7 March 2022 - Teva Pharmaceuticals announced today the launch of a first generic version of Revlimid (lenalidomide capsules), in 5 ...

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Novavax’s Covid-19 vaccine moves closer to FDA authorisation decision

6 March 2022 - Company says it has resolved manufacturing problems that led to earlier delays; FDA is reviewing shot’s authorisation ...

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Horizon Therapeutics announces FDA has granted priority review of the supplemental biologics license application for the concomitant use of Krystexxa (pegloticase injection) plus methotrexate for people living with uncontrolled gout

7 March 2022 - Application based on recent MIRROR randomised controlled trial results, which showed 71% of patients randomised to ...

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Servier announces FDA filing acceptance and priority review for Tibsovo (ivosidenib tablets) in combination with azacitidine for patients with previously untreated IDH1 mutated acute myeloid leukaemia

7 March 2022 - sNDA based on data from the global, Phase 3, AGILE trial evaluating Tibsovo in combination with ...

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U.S. Food and Drug Administration approves Opdivo (nivolumab) with chemotherapy as neo-adjuvant treatment for certain adult patients with resectable non-small cell lung cancer

4 March 2022 - Approval marks the first and only immunotherapy-based treatment for use before surgery for non-small cell lung cancer. ...

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Nymox announces submission of new drug application to the FDA for fexapotide triflutate

3 March 2022 - Nymox Pharmaceutical Corporation is pleased to announce today that it has submitted the Company’s new drug application ...

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Science hasn’t shown these medications work. They’re being sold anyway.

3 March 2022 - Federal regulators are increasingly approving medicines before studies have shown they work, leaving patients at risk ...

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Approved first generic for Apokyn injection cartridges requires separately packaged pen

24 February 2022 - The U.S. FDA has approved the first generic of Apokyn (apomorphine hydrochloride injection) drug cartridges to ...

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