by Mark Chiang

马克·蒋

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Takeda has announced positive results from a late-stage clinical trial for its experimental narcolepsy drug, Oveporexton. The findings pave the way for the company to seek regulatory approval for what could become the first treatment targeting orexin proteins, which play a key role in sleep regulation.

武田制药宣布其在研嗜睡症药物 Oveporexton 的后期临床试验取得了积极结果。这些发现为公司寻求监管批准铺平了道路，该药物有望成为首个靶向食欲素蛋白的治疗方法，而这种蛋白在睡眠调节中起着关键作用。

The study marks a significant milestone in narcolepsy research, as current therapies do not directly address orexin signaling deficiencies..

该研究标志着发作性睡病研究的一个重要里程碑，因为目前的治疗方法并未直接解决食欲素信号传导缺陷问题。

The Phase 3 trial evaluated Oveporexton’s efficacy and safety in patients with narcolepsy, a chronic neurological disorder characterized by excessive daytime sleepiness and sudden muscle weakness known as cataplexy. According to Takeda, the drug demonstrated favorable outcomes in managing these symptoms by targeting orexin proteins, which are involved in wakefulness and arousal.

第三阶段试验评估了Oveporexton在嗜睡症患者中的疗效和安全性，嗜睡症是一种慢性神经系统疾病，特征为白天过度嗜睡和被称为猝倒的突发性肌肉无力。根据武田制药的说法，该药物通过靶向与清醒和觉醒相关的食欲素蛋白，展示了在管理这些症状方面的良好效果。

This approach distinguishes Oveporexton from existing treatments that primarily focus on symptom management rather than addressing underlying biological mechanisms. Takeda plans to submit its findings to regulatory agencies as part of its application for market approval..

这种方法使Oveporexton不同于现有的主要专注于症状管理而非解决潜在生物学机制的治疗方法。武田计划将其研究结果提交给监管机构，作为其市场批准申请的一部分。

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Source: GO-AI-ne1

来源：GO-AI-ne1

Date: July 14, 2025

日期：2025年7月14日

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Mark Chiang

马克·江

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