CIDP Interim AnalysisPlanned interim responder analysis from the open-label portion of the CAPTIVATE CIDP study may validate clinical activity for claseprubart and serve as a near-term catalyst for regulatory advancement.
GMG Clinical Proof-of-conceptPositive Phase II MaGic trial results in generalized myasthenia gravis demonstrated proof-of-concept for claseprubart and support its potential as a best-in-class complement inhibitor.
Pipeline DiversificationAcquisition and licensing of DNTH212 broaden the pipeline with a mechanistically de‑risked asset targeting both adaptive and innate immunity, enhancing long-term development potential.