Eagle Pharmaceuticals receives additional FDA questions regarding vasopressin; court date set for 7 July 2021 in vasopressin trial

2 February 2021 - Company expects it will have 180 days of exclusivity. ...

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Geistlich Pharma granted FDA breakthrough device designation for Chondro-Gide articular cartilage cover

2 February 2021 - Geistlich Pharma announced that the Chondro-Gide articular cartilage cover has been granted a breakthrough device designation from ...

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Chinook receives rare paediatric disease designation from U.S. FDA for CHK-336 for treatment of primary hyperoxaluria

2 February 2021 - CHK-336 on track for Phase 1 clinical trial initiation in the second half of 2021. ...

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Cerecor announces fast track designation for CERC-803 for the treatment of leukocyte adhesion deficiency type II

2 February 2021 - Cerecor today announced that the U.S. FDA has granted fast track designation to CERC-803 for the treatment ...

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VBI Vaccines announces U.S. FDA acceptance of BLA filing for VBI’s 3 antigen prophylactic hepatitis B vaccine

2 February 2021 - FDA sets a target action date of 30 November 2021. ...

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Mirum Pharmaceuticals announces completion of rolling NDA submission for maralixibat in Alagille syndrome

1 February 2021 - Maralixibat U.S. launch expected in second half of 2021, if approved. ...

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Bristol Myers Squibb application for Zeposia (ozanimod) for the treatment of ulcerative colitis accepted for filing with priority review by U.S. FDA

1 February 2021 - U.S. Food and Drug Administration assigned an action date of 30 May 2021. ...

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Vyne Therapeutics announces FDA approval of Amzeeq (minocycline) label ppdate

1 February 2021 -  Vyne Therapeutics today announced approval by the U.S. FDA to include new information in the product ...

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Adamas announces FDA approval for second indication for Gocovri as an adjunctive treatment to levodopa/carbidopa in Parkinson’s disease patients experiencing OFF episodes

1 February 2021 - Gocovri is now the first and only medication approved to treat OFF and dyskinesia motor complications. ...

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Biogen announces FDA approval of Plegridy (peginterferon beta-1a) intramuscular administration for multiple sclerosis

1 February 2021 - Intramuscular injection Plegridy (peginterferon beta-1a) is now approved in the U.S. and the European Union, offering individuals ...

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Phase 1 drug candidate GLR2007 developed by Gan & Lee has been granted fast track designation by the U.S. FDA

29 January 2021 - Gan & Lee Pharmaceuticals today announced that the U.S. FDA has granted fast track designation for GLR2007, ...

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Biogen and Eisai announce FDA's 3 month extension of review period for the biologics license application for aducanumab

29 January 2021 - The new Prescription Drug User Fee Act action date set by the FDA is 7 June ...

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M6P Therapeutics receives six rare paediatric disease designations from the U.S. FDA for company’s deep pipeline of programs for lysosomal storage disorders

28 January 2021 - U.S. FDA also grants two orphan drug designations for the company’s gene therapy programs for Gaucher disease ...

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Bio-Thera Solutions announces FDA accepts biologics license application for BAT1706, a proposed biosimilar to Avastin

28 January 2021 - Bio-Thera Solutions today announced that the U.S. FDA has accepted its biologics license application for BAT1706, a ...

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Advocacy groups urge Biden administration not to tap Woodcock as FDA commissioner

27 January 2021 - As the Biden White House attempts to fashion its health policies, a coalition of consumer and ...

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