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Dianthus Therapeutics' stock rose after its Phase 3 trial for Claseprubart in CIDP met key interim goals with no serious side effects.
Dianthus Therapeutics shares rose after its Phase 3 CAPTIVATE trial for Claseprubart in CIDP met interim GO criteria, with 20 confirmed responders in Part A.
The company will expand the trial to up to 256 patients in Part A and randomize 128 in Part B, with no serious treatment-related adverse events.
Top-line data from Part B are expected by end of 2026.
Dianthus plans a registrational trial in generalized myasthenia gravis by mid-2026 and expects Phase 2 results for multifocal motor neuropathy in late 2026.
The company ended 2025 with $514 million in cash, supporting operations through 2028.
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Las existencias de Dianthus Therapeutics aumentaron después de que su ensayo de Fase 3 para Claseprubart en CIDP cumplió los objetivos intermedios clave sin efectos secundarios graves.