argenx SE announced positive topline results from the Phase 3 ADAPT OCULUS randomized, double-blind, placebo-controlled trial evaluating VYVGART (efgartigimod alfa and hyaluronidase-qvfc) administered subcutaneously in adults with ocular myasthenia gravis. The study met its primary endpoint, showing a statistically significant improvement versus placebo in the Myasthenia Impairment Index patient-reported ocular score at Week 4 (p=0.012). The company said the data will be presented at an upcoming medical meeting and plans to submit a supplemental Biologics License Application to the U.S. FDA to expand the product label to ocular myasthenia gravis.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. arGEN-X SE published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202602260030PRIMZONEFULLFEED1001166814) on February 26, 2026, and is solely responsible for the information contained therein.
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