Jazz Pharmaceuticals Completes FDA sBLA for Rylaze Dosing Schedule
Recently, Jazz Pharmaceuticals announced that the company completed the submission of a Supplemental Biologics License Application (sBLA) to the FDA seeking approval for a Monday/Wednesday/Friday IM dosing schedule for Rylaze. Learn more about its approval for use in patients with acute lymphoblastic leukemia and lymphoblastic lymphoma who have developed hypersensitivity to E coli–derived asparaginase.
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Long-Acting HIV Injectable Therapy Approved for Adolescents
The manufacturer, ViiV Healthcare, announced that the FDA approved Cabenuva for the treatment of HIV-1 in virologically suppressed adolescents who are aged 12 years or older and weigh at least 35 kg on a stable antiretroviral regimen, with no history of treatment failure, and with no known or suspected resistance to either cabotegravir or rilpivirine. Read more.
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