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Teva提交ecopipam治疗儿童抽动秽语症的NDA

2026-06-19 05:20

  • Teva Pharmaceutical Industries (TEVA) has submitted an NDA to the US FDA seeking approval of ecopipam for pediatric Tourette syndrome.
  • The application is supported by phase 3 data that found ecopipam significantly delayed time to relapse compared to placebo during an open-label treatment period. For up to 24 weeks, Ecopipam led to and sustained a meaningful reduction in the severity of tics.
  • Ecopipam is considered a first-in-class drug that works to inhibit dopamine signaling at the D1 receptor.

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