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BioWorld - Saturday, July 25, 2026
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Regulatory front for Nov. 18, 2019

Nov. 18, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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CHMP nods through five applications as EMA gets the keys to its new HQ

Nov. 18, 2019
By Cormac Sheridan
DUBLIN – Friday marked an important milestone for the EMA as its settles into its new home in Amsterdam. The Dutch authorities formally handed over to the agency the keys to its new building, which is located in the Zuidas district of the city.
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Novartis wins early FDA approval of P-selectin binder Adakveo in SCD

Nov. 18, 2019
By Randy Osborne
About two months ahead of the priority review action date, Novartis AG scored FDA clearance for Adakveo (crizanlizumab), previously known as SEG-101, to reduce the frequency of vaso-occlusive crises (VOCs), or pain crises, in adult and pediatric patients ages 16 and older with sickle cell disease (SCD).
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FDA approval of Shionogi antibacterial sets stage for move into new market

Nov. 18, 2019
By Michael Fitzhugh
Adults with complicated urinary tract infections (cUTIs) and limited or no alternative treatment options could soon receive Shionogi & Co. Ltd.'s cefiderocol following FDA approval for the antibacterial. The approved indication also included kidney infections caused by susceptible gram-negative microorganisms. The new therapy, to be marketed as Fetroja, is expected to be available in early 2020.
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Regulatory front for Nov. 15, 2019

Nov. 15, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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Gold capsules

Amarin gets adcom vote in favor of Vascepa to reduce CV events in adults with risk factors

Nov. 15, 2019
By Lee Landenberger
The FDA's Endocrinologic and Metabolic Drugs Advisory Committee (EMDAC) unanimously concluded Thursday that Amarin Corp. plc provided sufficient evidence of efficacy and safety to support approval of fish oil-based Vascepa (icosapent ethyl) for an indication to reduce the risk of cardiovascular (CV) events in adults with elevated triglyceride levels (≥135 mg/dL) and other risk factors for CV disease. The 16-0 vote followed a day's discussion about potential effects of mineral oil, about the proper age population and the value of labeling. EMDAC's conclusion is only an advisory, as the FDA makes the final decision. FDA representatives at the panel discussion noted the study provided convincing data and waived off most concerns about mineral oil's impact on LDL cholesterol levels and blood pressure.
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Regulatory front for Nov. 14, 2019

Nov. 14, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Nov. 13, 2019

Nov. 13, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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FDA clears first whole exome sequencing platform for overall tumor mutation burden

Nov. 13, 2019
By Meg Bryant
Nanthealth Inc. has received U.S. FDA clearance for a whole exome sequencing test to determine overall tumor mutational burden (TMB) in cancer tissue. Known as Omics Core, the first-of-its-kind in vitro diagnostic test is available now as part of Nanthealth's GPS Cancer molecular profiling suite.
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Regulatory front for Nov. 12, 2019

Nov. 12, 2019
The latest global regulatory news, changes and updates affecting biopharma.
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