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FDA grants breakthrough status to Biogen’s litifilimab for severe skin lupus, speeding its development.
The FDA has granted Breakthrough Therapy Designation to litifilimab, a Biogen-developed monoclonal antibody, for treating cutaneous lupus erythematosus, a chronic autoimmune skin condition without approved targeted therapies.
The designation, based on Phase 2 LILAC study results, aims to speed development and review.
The drug, which targets BDCA2 on dendritic cells, is being studied in a Phase 3 trial with results expected in 2027.
Biogen’s stock rose slightly following the announcement.
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La FDA otorga estatus de avance al litifilimab de Biogen para el lupus cutáneo grave, acelerando su desarrollo.