Verrica Pharmaceuticals完成Ycanth®治疗寻常疣的首个关键性III期试验（Cove-2）入组，顶线数据预计2027年第一季度公布

美股速递08-27

Verrica Pharmaceuticals宣布，其评估Ycanth®用于治疗寻常疣的首个关键性III期临床试验（Cove-2）已圆满完成患者入组。公司预计，该试验的顶线数据将在2027年第一季度对外公布。

这一里程碑标志着Verrica Pharmaceuticals在推进Ycanth®治疗常见皮肤疾病方面迈出了关键一步。Cove-2试验作为验证Ycanth®疗效与安全性的重要临床项目，其顺利入组为后续数据读出奠定了坚实基础。

随着入组工作的收官，研究团队正全力推进后续随访与数据收集流程。业界普遍关注这项试验的最终结果，因为它不仅关系到Ycanth®的监管审批前景，更可能为寻常疣患者带来新的治疗选择。Verrica Pharmaceuticals对这一进展表示乐观，并将持续致力于为患者提供创新疗法。

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