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BioWorld - Friday, July 10, 2026
Home » Topics » Regulatory

Regulatory
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BARDA deal could provide T2 Biosystems up to $69M

Sep. 16, 2019
By Meg Bryant

Regulatory front

Sep. 16, 2019

FDA expands Nucala label to include younger children

Sep. 16, 2019
By Michael Fitzhugh
Glaxosmithkline plc has won FDA approval to market Nucala (mepolizumab) for use in children as young as 6 with severe eosinophilic asthma (EA). The therapy already had FDA approval as an add-on maintenance treatment for kids with the same condition ages 12 and older. Approval of the sBLA, submitted last November, catches the U.S. market up to the EU, where Nucala has been approved as an add-on treatment for children ages 6 to 17 since August 2018.
Read More

FDA approves Ibsrela for irritable bowel syndrome with constipation

Sep. 13, 2019

FDA retains 'well-defined' restriction in special 510(k) final

Sep. 13, 2019
By Mark McCarty

Health of U.S. patent system in the eye of the beholder

Sep. 13, 2019
By Mari Serebrov
Depending on who's talking, the U.S. patent system may, or may not, be in dire need of reform. In a Senate Judiciary subcommittee hearing Wednesday on the bipartisan STRONGER Patents Act, Sen. Chris Coons (D-Del.) stressed the need to undo the precedent set by the Supreme Court's 13-year-old eBay decision that weakened injunctive relief in infringement cases and to resolve some of the unintended consequences of the 2011 America Invents Act (AIA).
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Product regulatory actions for Sept. 12, 2019

Sep. 13, 2019

Health of U.S. patent system in the eye of the beholder

Sep. 13, 2019
By Mari Serebrov
Depending on who's talking, the U.S. patent system may, or may not, be in dire need of reform. In a Senate Judiciary subcommittee hearing Wednesday on the bipartisan STRONGER Patents Act, Sen. Chris Coons (D-Del.) stressed the need to undo the precedent set by the Supreme Court's 13-year-old eBay decision that weakened injunctive relief in infringement cases and to resolve some of the unintended consequences of the 2011 America Invents Act (AIA).
Read More

FDA approves Xeris' Gvoke, first ready-to-use stable liquid glucagon for severe hypoglycemia

Sep. 12, 2019

Product regulatory actions for Sept. 11, 2019

Sep. 12, 2019
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