---
title: "Celon Pharma Says FDA Deems Phase III Study Concept For CPL'36 Treatment Reasonable"
type: "News"
locale: "zh-HK"
url: "https://longbridge.com/zh-HK/news/275925527.md"
datetime: "2026-02-13T16:18:43.000Z"
locales:
  - [zh-CN](https://longbridge.com/zh-CN/news/275925527.md)
  - [en](https://longbridge.com/en/news/275925527.md)
  - [zh-HK](https://longbridge.com/zh-HK/news/275925527.md)
---

> 支持的語言: [简体中文](https://longbridge.com/zh-CN/news/275925527.md) | [English](https://longbridge.com/en/news/275925527.md)


# Celon Pharma Says FDA Deems Phase III Study Concept For CPL'36 Treatment Reasonable

Feb 13 (Reuters) - Celon Pharma SA (CLNP.WA) : \* ANNOUNCES COMPLETION OF ANALYSIS OF WRITTEN RESPONSES FROM FDA REGARDING CPL'36 FOR PARKINSON'S DISEASE-INDUCED DYSKINESIA (PD-LID) \* FDA DEEMS PROPOSED PHASE III STUDY CONCEPT FOR CPL'36, INCLUDING DESIGN, DURATION, AND PRIMARY ENDPOINT, AS REASONABLE \* BELIEVES FDA STANCE SUPPORTS CONTINUING PHASE III PROGRAM AND WILL INCORPORATE RECOMMENDATIONS INTO PROTOCOLS Source text: Further company coverage: (CLNP.WA)

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