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FDA grants breakthrough status to Praxis' drug for essential tremor, showing strong results in trials.
Praxis Precision Medicines has received FDA Breakthrough Therapy Designation for ulixacaltamide, a drug candidate treating essential tremor, a condition affecting millions of Americans.
The designation, based on positive Phase 3 trial results, highlights the drug’s potential to significantly improve tremor symptoms and daily functioning, with better sustained effects than placebo.
The FDA’s recognition underscores the need for more effective treatments, as current options often fall short.
Praxis plans to submit a regulatory approval application in early 2026 and expects continued development progress.
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La FDA otorga estatus de avance al medicamento de Praxis para el temblor esencial, mostrando fuertes resultados en ensayos.