- Biogen disclosed positive Phase 2 results from AMETHYST Part A testing litifilimab in cutaneous lupus erythematosus, supporting its ongoing Phase 3 program.
- Data were presented at 2026 American Academy of Dermatology Annual Meeting.
- Trial met primary endpoint at Week 16, with 14.7% of litifilimab patients reaching clear or almost clear skin versus 2.9% on placebo.
- Biogen cited an FDA Breakthrough Therapy Designation for litifilimab, positioning it as a potential first targeted therapy for CLE.
- Safety profile remained broadly consistent with prior studies, with serious adverse events reported in 6.8% of litifilimab patients versus 2.9% on placebo through Week 24.
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. Biogen Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603281500PRIMZONEFULLFEED9680264) on March 28, 2026, and is solely responsible for the information contained therein.
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