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Neurizon seeks FDA approval for ALS drug NUZ-001, targeting TDP-43 protein aggregation.
Neurizon, a biotech firm, has submitted an IND application to the FDA for its ALS treatment candidate NUZ-001, aiming to start a Phase 2/3 clinical trial in the HEALEY ALS Platform Trial.
NUZ-001 targets TDP-43 protein aggregation.
If cleared, Massachusetts General Hospital will file a protocol amendment in Q1 2025, with patient enrollment expected in the first half of 2025.
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Neurizon busca la aprobación de la FDA para el fármaco ALS NUZ-001, dirigido a la agregación de proteínas TDP-43.