A phase III clinical trial of PXT3003 in Chinese patients with Charcot-Marie-Tooth disease type 1A

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Authors: Xiaoxuan Liu, Wanqian Cao, Hongli Li, Chen Sun, Jingzheng Hao, Yuwei Da, Baoyu Yuan, Ning Wang, Shan Wu, Jun Liu, Zuneng Lu, Qi Fang
+18 more Zhi‐Ying Wu, Liying Yuan, Jiaoting Jin, Haishan Jiang, Yaling Liu, Mingming Ma, Wei Ling, Jianglong Tu, Xiaoli Yao, Yuan Sun, Xuefan Yu, Yiming Liu, Di Zhong, Yun Xu, Yuming Xu, Runxiu Zhu, Dongsheng Fan, Ruxu Zhang
Cited by: 1
References: 20

Abstract

Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited peripheral neuropathy and currently lacks disease-modifying therapy. PXT3003, a low-dose oral combination targeting PMP22 overexpression, has shown efficacy in two trials, while one recent confirmatory trial failed to meet its primary efficacy endpoints. In this trial, eligible participants aged 16 to 65 years with genetically confirmed mild-to-moderate CMT1A were randomly assigned to receive oral PXT3003 or placebo twice daily for 15 months. The primary endpoint was the change in the overall neuropathy limitations scale (ONLS) total score from baseline to month 15. At month 15, mean ONLS change from baseline was −0.268 (SD: 0.82) in the PXT3003 group versus 0.013 (SD: 0.65) in the placebo group, with a between-group difference of −0.249 (95% confidence interval [CI]: −0.467 to −0.030; p = 0.0257). Significant improvements were observed in the ONLS leg subscore and ankle-dorsiflexion strength. These findings support PXT3003 as a promising therapeutic option for alleviating limb symptoms in patients with CMT1A.

Fields of Study & Subjects

Hereditary Neurological Disorders Peripheral Neuropathies and Disorders Nuclear Structure and Function

Publication details

Journal / source
iScience
Publisher
Elsevier BV
Volume
29
Issue
9
Pages
117284–117284
Publication date
27 August 2026
Language
EN