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The FDA approved Neurizon’s NUZ-001 for a major ALS trial testing new treatments.
The FDA has approved Neurizon Therapeutics’ NUZ-001 to enter the HEALEY ALS Platform Trial, a multicenter, adaptive study testing potential ALS treatments.
The drug, which targets TDP-43 aggregation and impaired autophagy, showed promising safety and brain penetration in early data.
Site activations and patient enrollment are expected to begin in early 2026.
The trial, led by Mass General Brigham and NEALS, aims to speed up drug development by testing multiple therapies simultaneously.
NUZ-001 remains investigational and is not yet approved for sale.
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La FDA aprobó Neurizon® NUZ-001 para un importante ensayo de ELA para probar nuevos tratamientos.