On Aug. 7, 2018, the U.S. District Court in Delaware ruled against Shire in its request for a preliminary injunction against Roche AG from creating, transporting and marketing its recently-approved drug Hemlibra in the U.S., which received FDA approval to treat people with hemophilia A with inhibitors in 2017. This ruling means there are no legal limitations on the ability of physicians to prescribe Hemlibra at this time.
For more information on the Roche/Genentech and Shire injunction filing, click here.
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