Tukvadze Nestani, Mashatole Sehlomola, Jacobs Anne, Ngwanto Tlhago, Heinrich Norbert, Van Rie Annelies, Crudu Valeriu, Tudor Elena, Goginashvili Leila, Ibraim Elmira, Khosa Celso, Howell Pauline, Rajaram Shakira, Naidoo Kinita, Niemann Stefan, Reither Klaus, Wallis Robert S
Swiss Tropical and Public Health Institute, Kreuzstrasse 2, 4123, Allschwil, Switzerland.
University of Basel, Petersplatz 1, 4001, Basel, Switzerland.
BMC Infect Dis. 2025 May 28;25(1):768. doi: 10.1186/s12879-025-11072-5.
Tuberculosis (TB) is a leading cause of morbidity and mortality worldwide. Current TB treatments are inadequate, requiring participants closely adhere to multi-drug regimens that are long, complex, and often poorly tolerated. In addition to these well-recognized shortcomings, current TB treatments, particularly those for rifampicin-resistant tuberculosis, leave a majority of cured participants with permanent, clinically significant lung impairment and radiographic evidence of bronchiectasis and fibrosis. This project will determine if two adjunctive host-directed therapies (HDTs) can prevent these poor outcomes.
Three hundred thirty participants with RIF-R TB and baseline risk factors for poor outcome will be enrolled in a randomized, controlled, 3-armed multi-centre trial, with clinical sites in Romania, Moldova, Georgia, Mozambique, and South Africa. All participants will receive standard multidrug therapy according to national guidelines. Those participants randomized to the experimental arms will in addition receive either CC-11050 (dovramilast) or metformin. Co-primary efficacy endpoints will examine effects on lung function (measured by spirometry) and infection (measured as time to stable sputum culture conversion). A sub-study will examine quantitative change in lung radiodensity by CT scan.
These selected host-directed therapies candidates represent two complementary strategies: reducing inflammation vs inducing host cell anti-microbial activity, respectively. Both candidates are supported by data from preclinical and clinical studies. If successful, this ground-breaking project will increase Europe's capacity to control drug resistant tuberculosis by developing new treatments that increase the likelihood of cure and reduce the risk of life-long disability.
EudraCT Number: 2020-004295-18. South African National Clinical Trial Registration (SANCTR) Number: DOH-27-042021-8345.
结核病是全球发病和死亡的主要原因。目前的结核病治疗方法并不充分,要求参与者严格遵守冗长、复杂且耐受性通常较差的多药治疗方案。除了这些广为人知的缺点外,目前的结核病治疗方法,尤其是针对耐利福平结核病的治疗方法,会使大多数治愈的参与者留下永久性的、具有临床意义的肺部损伤以及支气管扩张和纤维化的影像学证据。该项目将确定两种辅助宿主导向疗法(HDTs)是否可以预防这些不良后果。
330名患有耐利福平结核病且有不良预后基线风险因素的参与者将被纳入一项随机、对照、三臂多中心试验,临床地点位于罗马尼亚、摩尔多瓦、格鲁吉亚、莫桑比克和南非。所有参与者将根据国家指南接受标准的多药治疗。随机分配到试验组的参与者还将额外接受CC-11050(多夫拉司特)或二甲双胍。共同主要疗效终点将检查对肺功能(通过肺活量测定法测量)和感染(以痰培养稳定转阴时间测量)的影响。一项子研究将通过CT扫描检查肺放射性密度的定量变化。
这些选定的宿主导向疗法候选药物代表了两种互补策略:分别是减轻炎症和诱导宿主细胞抗菌活性。两种候选药物均得到临床前和临床研究数据的支持。如果成功,这个开创性的项目将通过开发新的治疗方法来提高欧洲控制耐药结核病的能力,这些新治疗方法可提高治愈的可能性并降低终身残疾的风险。
欧盟临床试验注册号:2020-004295-18。南非国家临床试验注册号(SANCTR):DOH-27-042021-8345。