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临床试验/NCT01380119
NCT01380119已完成2 期

Phase 2 Study of Orally Formulated Heat-killed Mycobacterium Vaccae Study in TB Patients

Lisichansk Regional Tuberculosis Dispensary1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2011年8月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
sputum conversion

研究概览

简要总结

This is a phase II, randomized, placebo-controlled trial, aimed to seek the therapeutic benefit of V7 in combination with standard of care anti-Tuberculosis (TB) therapy (ATT) among Mycobacterium tuberculosis-infected sputum smear positive subjects. The results will be compared to placebo combined with standard ATT therapy. The trial will consist of one stage with sputum evaluation at months 1 and 2.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects who are at least 18 years old and are willing and capable of providing informed consent. Both men and non-pregnant women will be included.
  • TB infection documented prior to Study Entry by sputum smear positive for acid-fast bacilli (AFB) test.
  • TB score status at baseline.
  • Agreement to participate in the study and to give a sample of blood for lab testing.
  • Readily available home or other address where patient can be found.

排除标准

  • Subjects who might have already taken V5 in prior trial and have no baseline data. Pregnant or breast-feeding women are excluded.
  • Subjects who have taken study unrelated drugs or immunomodulatory therapies during study or prior to Entry.
  • Medical conditions such as active alcohol or substance abuse, or psychological issues that in the opinion of the local investigator would interfere with adherence to the requirements of this study.

结局指标

主要结局

sputum conversion

时间窗: 2 months

To compare the efficacy of combination of V7 with anti-TB treatment versus anti-TB treatment+placebo in adults with pulmonary tuberculosis including:

次要结局

  • safety(1 and 2 months)

研究者

发起方
Lisichansk Regional Tuberculosis Dispensary
申办方类型
Other
责任方
Sponsor

研究点 (1)

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