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BioWorld - Thursday, May 7, 2026
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SK Biopharma partner wins European approval for drug-resistant focal-onset seizure treatment

April 6, 2021
By Gina Lee
HONG KONG – SK Biopharmaceuticals Co. Ltd. partner Arvelle Therapeutics GmbH, now part of Angelini Pharma, has received European Commission (EC) approval for Ontozry (cenobamate), a treatment for drug-resistant focal-onset seizures. The approval was granted for focal-onset seizures with or without secondary generalization in adults who have not been adequately controlled despite a history of treatment with at least two anti-epileptic medicines.
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Regulatory front for April 6, 2021

April 6, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA adds fingerstick sample to roster of COVID EUAs; NICE: Sonata system not backed by head-to-head studies.
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Regulatory actions for April 6, 2021

April 6, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Philips, Roche.
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Patent law book and gavel

Proposed NIST rule escalates debate over Bayh-Dole march-in

April 6, 2021
By Mari Serebrov
Nearly 16,500 groups and individuals put in their two cents on a proposed National Institute of Standards and Technology (NIST) rule clarifying that the U.S. government, under the Bayh-Dole Act, can’t march in on patents derived from federally funded research just because it doesn’t consider the price of the resulting product “reasonable.”
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European Commission headquarters

Europe gears up for MCMs of the future

April 6, 2021
By Mari Serebrov
The European Commission opened a public consultation to help it develop the Health Emergency Preparedness and Response Authority, a new initiative to better prepare Europe for cross-border health threats.
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Architectural pillars

Regulatory front for April 6, 2021

April 6, 2021
The latest global regulatory news, changes and updates affecting biopharma in Asia, including: Global Health Innovative Technology Fund, Health Canada, Therapeutic Goods Administration.
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Regulatory actions for April 6, 2021

April 6, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Antengene, Bioniz, Gan & Lee, Huyabio, Landos, Mitoimmune, Ortho Regenerative, Tarus.
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FDA approves Qelbree for the treatment of ADHD in pediatric patients

April 6, 2021
Device image

Orthofix gets approval for Construx 3D cervical spacer

April 5, 2021
By Greg Goth
The FDA has granted 510(k) clearance to Orthofix Medical Inc.’s Construx Mini Ti spacer system for anterior cervical discectomy and fusion (ACDF) procedures. Company documents claim the implant has an optimized porosity and pore size, which creates a 3D porous surface with the potential for bone ingrowth.
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Regulatory front for April 5, 2021

April 5, 2021
By Holland Johnson
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: COVID-19 inventions included in USPTO awards program; First thrombosis incident reported in Australia; FDA revises Moderna EUA; GAO refuses to reconsider VA challenge.
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