argenx reports positive Phase 3 ADAPT OCULUS results for VYVGART in ocular myasthenia gravis

Reuters03-06 14:00
argenx reports positive Phase 3 ADAPT OCULUS results for VYVGART in ocular myasthenia gravis

argenx SE announced it will present new clinical data at the 2026 American Academy of Neurology Annual Meeting (April 18-22, Chicago) on VYVGART (efgartigimod) in myasthenia gravis and chronic inflammatory demyelinating polyneuropathy, as well as on pipeline candidates empasiprubart and adimanebart. The company said positive Phase 3 ADAPT OCULUS results indicate VYVGART’s potential in adults with ocular myasthenia gravis, and additional Phase 3 ADAPT SERON data support efficacy and safety in generalized myasthenia gravis patients without detectable AChR antibodies across MuSK+, LRP4+, and triple seronegative subtypes; these results will be presented at the meeting. argenx also plans to present CIDP analyses from the ADHERE program, including a post hoc assessment in treatment-naïve patients and biomarker and real-world evidence, and to share additional Phase 1b data for adimanebart (ARGX-119) in DOK7 congenital myasthenic syndromes.

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: 202603060100PRIMZONEFULLFEED1001168541) on March 06, 2026, and is solely responsible for the information contained therein.

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