A Phase III Placebo-controlled, Double-blind, Randomized Trial to Evaluate the Efficacy and Safety of TMC207 in Subjects With Sputum Smear-positive Pulmonary Infection With Multi-drug Resistant Mycobacterium Tuberculosis (MDR-TB)
试验速览
- 阶段
- 3 期
- 状态
- 撤回
- 发起方
- 试验地点
- 44
- 主要终点
- Number of patients with favorable treatment outcome at Week 60
研究概览
简要总结
The purpose of this study is to provide safety and efficacy data for TMC207 and to demonstrate that TMC207 added to a background regimen (BR) is superior to treatment with the BR plus placebo.
详细描述
This is a randomized (individuals will be assigned by chance to study treatments), double-blind (individual and investigator will not know the identity of study treatments), placebo (substance containing no active medication)-controlled, 2-arm study in patients with sputum smear-positive pulmonary infection with multi-drug resistant tuberculosis (MDR-TB) defined as tuberculosis (TB) due to infection with a strain of Mycobacterium tuberculosis (M. tuberculosis) that is resistant to both isoniazid and rifampin, or pre-extensively drug resistant (pre-XDR-TB) defined as TB due to infection with an MDR strain of M. tuberculosis that is resistant either to at least one of the injectable second-line drugs [amikacin, kanamycin, or capreomycin] or to any fluoroquinolone, but not both). Approximately 600 patients with sputum smear-positive pulmonary infection with MDR-TB or pre-XDR TB will receive a background regimen (BR) of MDR-TB therapy and will be randomly assigned in a 1:1 ratio to one of 2 treatment arms (Arms A [TMC207 + BR] and B [placebo + BR]). All patients will receive TMC207 or placebo in combination with a BR of MDR-TB therapy. TMC207 (or matching placebo) will be taken as oral tablets at a once daily dose of 400 mg for the first 2 weeks and 200 mg 3 times/week for the remaining period of TMC207 (or matching placebo) administration. The study will consist of a screening phase of a maximum of 3 weeks, a 36-week double-blind treatment phase, followed by a 48-week follow-up phase up to Week 84, also referred to as the treatment-free follow-up. After the treatment-free follow-up phase, there will be a safety follow-up phase of 48 weeks up to Week 132. Patients from Arms A or B who fail treatment according to prespecified criteria will be given the option to receive 24 weeks of TMC207 plus an individualized salvage regimen taken for a duration consistent with national TB guidelines. Efficacy and pharmacokinetic evaluations will be performed at time points as detailed in the protocol. Safety will be monitored throughout the study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with sputum smear-positive pulmonary Mycobacterium multi-drug resistant tuberculosis; including pre-extensively drug resistant TB, and positive for acid fast bacilli on direct smear examination of expectorated or induced sputum specimen (>=1+ smear positive within the preceding 3 weeks) at screening and also on Day -1
排除标准
- •Has known infection with extensively drug resistant tuberculosis isolate
- •Has a clinically significant active medical condition such as, but not limited to, hepatic, pancreatic, renal, cardiovascular, gastrointestinal, hematologic, neurologic, locomotor, immunologic, ophthalmologic (e.g., corneal opacification or ulcers, uveitis, chorioretinitis), metabolic (except stable diabetes based on the investigator's judgement), endocrine, oncological disease, muscular disease (e.g., myositis, rhabdomyolysis), or psychiatric, dermatological illness, or any other illness that the investigator considers should exclude the patient or that could interfere with the interpretation of the study results. Eligibility of patients with poorly controlled diabetes as indicated by hemoglobin A1c higher than the normal range at screening should be based on the investigators judgment
结局指标
主要结局
Number of patients with favorable treatment outcome at Week 60
时间窗: Week 60
次要结局
- Number of patients with confirmed culture conversion by geographic region(Up to Week 132)
- Number of patients with confirmed culture conversion by human immunodeficiency virus status(Up to Week 132)
- Number of patients with improvements in laboratory assessments at Week 36 and at the end of the treatment-free follow up(Up to Week 132)
- Number of patients with improvements in chest radiograph assessments at Week 36 and at the end of the treatment-free follow up(Up to Week 132)
- Number of patients that received salvage regimen with favorable treatment outcome 24 weeks after the end of the individualized salvage regimen(Up to Week 132)
- Number of tuberculosis-related deaths per investigator assessment(Up to Week 132)
- Number of patients with weight gain (greater than 5 percent) at Week 36 and at the end of the treatment-free follow up(Up to Week 132)
- Number of patients with confirmed culture conversion at Week 60 or at time of trial discontinuation(Up to Week 132)
- Number of patients with confirmed culture conversion at Week 84(Week 84)
- The number of patients with development of pre-extensively drug-resistant tuberculosis and extensively drug-resistant tuberculosis(Up to Week 132)
- Time to sputum culture conversion(Up to Week 132)
- Number of patients with negative culture and smear for tuberculosis(Up to Week 132)
- Time to positive signal in Mycobacteria Growth Indicator Tube (MGIT960)(Up to Week 132)
- Number of patients with confirmed culture conversion by lung cavity status(Up to Week 132)
- Number of patients with confirmed culture conversion by baseline resistance to anti-tuberculosis therapy(Up to Week 132)
- Number of patients with Tuberculosis Symptom Profile symptoms at Week 36 and at the end of the treatment-free follow up(Up to Week 132)
- Mean plasma concentrations of TMC207(Up to Week 36)
- Mean plasma concentrations of N-monodesmethyl metabolite of TMC207(Up to Week 36)
- Number of patients affected by an adverse event(Up to Week 132)
- Number of patients with confirmed culture conversion at Week 36(Up to Week 132)
- Number of patients who required lung surgeries (resection or pneumonectomy) during the study(Week 132)
- Number of patients with confirmed culture conversion by baseline albumin grade(Up to Week 132)
- Number of patients with confirmed culture conversion at Week 132(Week 132)
- Number of patients with confirmed culture conversion by baseline TMC207 minimal inhibitory concentration(Up to Week 132)
- Number of patients who experienced death(Up to Week 132)
- Number of patients will be qualified as cure based on the WHO outcome definition and the number of treatment failures, deaths, transfer out/defaults, and treatment completed(Up to Week 132)