结核与肺部疾病杂志  2026, Vol. 7 Issue (5): 574-580    DOI: 10.19983/j.issn.2096-8493.20260098

• 研究方案 • 上一篇    下一篇

口服舒达吡啶(WX-081)片对初治药物敏感肺结核和耐药肺结核早期杀菌活性、安全性和耐受性的Ⅱ期临床研究

曾春梅1, 卢青霞1, 聂文娟2, 朱庆东1(), 初乃惠2(), 朱凤梅1()   

  1. 1 南宁市第四人民医院结核科, 南宁 530023
    2 首都医科大学附属北京胸科医院结核一科, 北京 101149
  • 收稿日期:2026-05-12 出版日期:2026-10-20 发布日期:2026-10-19
  • 通信作者: 朱庆东,初乃惠,朱凤梅 E-mail:zhuqingdong2003@163.com;dongchu1994@sina.com;59611427@qq.com
  • 基金资助:
    广西重点研发计划(桂科 AB25069097);北京市卫生健康委员会登峰项目(G202511062);北京市卫健委研究型病房卓越临床研究计划(BRWEP2024W042160109);北京市通州区科技计划项目(WS2025017)

A phase Ⅱ clinical study on the early bactericidal activity, safety, and tolerability of oral sudapyridine (WX-081) tablets in patients with newly diagnosed drug-susceptible and drug-resistant pulmonary tuberculosis

Zeng Chunmei1, Lu Qingxia1, Nie Wenjuan2, Zhu Qingdong1(), Chu Naihui2(), Zhu Fengmei1()   

  1. 1 Department of Tuberculosis, Nanning Fourth People’s Hospital, Nanning 530023, China
    2 Department Ⅰ of Tuberculosis, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China
  • Received:2026-05-12 Online:2026-10-20 Published:2026-10-19
  • Contact: Zhu Qingdong,Chu Naihui,Zhu Fengmei E-mail:zhuqingdong2003@163.com;dongchu1994@sina.com;59611427@qq.com
  • Supported by:
    Key Research and Development Program of Guangxi Zhuang Autonomous Region (Gui Ke AB25069097);Beijing Municipal Health Commission Dengfeng Program(G202511062);Beijing Municipal Health Commission Excellent Clinical Research Program for Research-oriented Wards(BRWEP2024W042160109);Beijing Tongzhou District Science and Technology Program Project(WS2025017)

摘要:

背景: 耐药结核病是全球重大公共卫生挑战,治疗方案存在疗程长、不良反应多等问题。舒达吡啶(WX-081)是我国首个Ⅰ类抗结核新药,具有较好抗结核活性和相较贝达喹啉更好的安全性。方法: 本研究为一项全国随机、对照、多中心Ⅱ期临床试验,旨在评估口服舒达吡啶片对初治药物敏感肺结核和利福平耐药/耐多药肺结核患者的早期杀菌活性、安全性和耐受性,并初步评价其对耐药肺结核患者的有效性。研究通过收集单药治疗过程中,以及包含新药方案早期治疗后的痰菌菌落形成单位和痰培养报阳时间,观察变化趋势,并与经典治疗方案做比较,从而评价药物抗结核活性,并在治疗过程中收集安全性和耐受性数据用于评价用药安全。讨论: 本研究期望验证抗结核新药、优化耐药肺结核治疗方案,从而在保证抗结核活性的情况下提高用药安全性,进而为提高耐药肺结核治愈率提供理论依据和临床数据。

关键词: 抗结核药, 结核,抗多种药物性, 随机对照试验, 舒达吡啶

Abstract:

Background: Drug-resistant tuberculosis (TB) is a significant global public health challenge, with treatment regimens often characterized by long durations and numerous adverse effects. Sudapyridine (WX-081) is China’s first Class Ⅰ novel anti-tuberculosis drug, demonstrating good anti-tuberculosis activity and better safety compared to bedaquiline. Methods: This study is a national, randomized, controlled, multicenter Phase Ⅱ clinical trial, aiming to evaluate the early bactericidal activity, safety, and tolerability of oral sudapyridine tablets in patients with newly diagnosed drug-susceptible and drug-resistant pulmonary tuberculosis, and to preliminarily assess its effectiveness in patients with drug-resistant tuberculosis. The study collects data on sputum colony-forming units and time to positivity during monotherapy and early treatment with the new drug regimen, observing trends and comparing them with classic treatment regimens to evaluate anti-tuberculosis activity. Safety and tolerability data are also collected during treatment to assess the safety of the drug. Discussion: This study aims to validate the new anti-tuberculosis drug and optimize treatment regimens for drug-resistant pulmonary tuberculosis. By ensuring anti-tuberculosis activity while improving drug safety, it provides theoretical basis and clinical data to increase the cure rate of drug-resistant pulmonary tuberculosis.

Key words: Antitubercular agents, Tuberculosis, multidrug-resistant, Randomized controlled trial, Sudapyridine

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