A Phase III Trial in Subjects Suspected to Have Tuberculosis, Comparing the Diagnostic Performance of C-Tb to QuantiFERON®-TB Gold In-Tube, in Combination With a Double Blind Randomized Split Body Safety Assessment of C-Tb Versus 2 T.U. Tuberculin PPD RT23 SSI (PPD)
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 1,190
- 试验地点
- 9
- 主要终点
- To evaluate the diagnostic performance of C-Tb in relation to age, HIV and CD4 counts
研究概览
简要总结
Tuberculosis (TB) continues to be one of the most serious bacterial infections worldwide and therefore new improved diagnostic tests are needed to help doctors in diagnosing TB.
The new skin test is named C-Tb. Like the current tuberculin skin test, PPD, the C-Tb test is injected just under the skin and will, when positive, show redness and/or swelling at the injection site while a negative test will leave no reactions. The investigators hope that this new C-Tb skin test will be more precise (specific) than the PPD test, as the PPD test e.g. may show a reaction if the person tested is BCG vaccinated.
The aim of this trial is to test the C-Tb skin test in volunteers suspected of having TB disease.
With focus on age, HIV status and CD4 count the following analyses are done (in an overall perspective):
- To compare the C-Tb test to a blood test, the QuantiFERON test.
- To compare the C-Tb test to the PPD test that is currently being used.
- To assess the safety of the C-Tb test.
详细描述
The TESEC-05 trial is an open comparison of the diagnostics performance of C-Tb compared to the QuantiFERON®-TB Gold In-Tube, in combination with a double-blind randomized split-body safety assessment of C-Tb versus to 2 T.U. Tuberculin PPD RT23 SSI.
The trial is a multi-centre Phase III clinical trial designed specifically to address C-Tb in relation to the paediatric population and to HIV infection. The intention is to evaluate how the C-Tb test performs in the paediatric population with respect to safety, and to ensure that SSI will be able to extrapolate data obtained in an adult population to the paediatric population.
Furthermore, the intention is both to evaluate the diagnostic performance and safety of C-Tb in HIV infected individuals and to evaluate whether SSI will be able to extrapolate data obtained in a non-HIV population to a HIV population.
The trial population will consist of paediatric participants with suspected TB infection and adult participants suspected to have TB disease. Furthermore a control group of 100 children between 5 - 11 years of age with no symptoms or known exposure will be recruited from an area with a "low" prevalence of TB (an area with an incidence rate < 299/100,000 per year, the average rate of TB in South Africa in 2005 was 645/100,000 per year.
The trial will be conducted in South Africa where the prevalence of HIV infection is high and MTb infections are endemic.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 28 Days 至 65 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •HIV NEGATIVE PARTICIPANTS:
- •Participants between 5 and 65 years attending the TB clinic due to suspicion of TB disease
- •Infants, toddlers and children between 28 days and 4 years must either have symptoms or signs of TB or be in close contact to a smear positive pulmonary TB case (more than 6 hours/day for at least five days)
- •Is between 28 days and 65 years of age
- •Participant, parent or legal guardian has signed the informed consent
- •Is HIV negative confirmed by two rapid tests. However, children between 28 days and 4 years may have an unknown HIV status and may receive antiretroviral therapy (ART) or have breastfeeding mothers on ART
- •Is willing and likely to comply with the trial procedures
- •Is prepared to grant authorized persons access to their medical record
- •HIV POSITIVE PARTICIPANTS:
- •Participants between 5 and 65 years attending the TB clinic due to suspicion of TB disease
- •Infants, toddlers and children between 28 days and 4 years must either have symptoms* or signs** of TB or be in close contact to a smear positive pulmonary TB case (more than 6 hours/day for at least five days)
- •Is between 28 days and 65 years of age
- •Participant, parent or legal guardian has signed the informed consent
- •Is HIV positive confirmed by:
- •two positive rapid tests or
- •1 positive rapid test and an additional confirmatory ELISA test
- •A CD4 count has been done
- •Is willing and likely to comply with the trial procedures
- •Is prepared to grant authorized persons access to their medical record
- •HIV NEGATIVE CONTROL GROUP:
- •Participant with no known contact to people infected with MTb and no signs or symptoms of TB.
- •Is between 5 and 11 years of age
- •Participant, parent or legal guardian has signed the informed consent
- •Is HIV negative confirmed by two rapid tests
- •Is willing and likely to comply with the trial procedures
- •Is prepared to grant authorized persons access to their medical record
排除标准
- •HIV NEGATIVE PARTICIPANTS:
- •Has a confirmed diagnosis of tuberculosis at Screening Visit
- •Has been vaccinated with a live vaccine within 6 weeks prior to the day of inclusion (e.g. MMR, yellow fever, oral typhoid vaccines) except BCG vaccine
- •Has been tuberculin (TST) tested less than 12 months prior to the day of inclusion
- •Is pregnant, breastfeeding or intending to get pregnant during the trial period
- •Is a female of child bearing potential (12 years of age or older) not willing to use effective barrier (including spermicidal gel), hormonal or intrauterine contraceptive measures during the trial period
- •Has an active disease affecting the lymphoid organs (e.g., Hodgkin's disease, lymphoma, leukaemia, sarcoidosis)
- •Has a current skin condition which interferes with the reading of the C-Tb and PPD e.g. tattoos, severe scarring, burns/sunburns, rash, eczema, psoriasis, or any other skin disease at or near the injection sites
- •Has a condition where blood drawings pose more than minimal risk for the participant, such as haemophilia, other coagulation disorders or significantly impaired venous access
- •Currently participating in another clinical trial with an investigational or non-investigational drug or device or has participated in another clinical trial within the 3 months prior to dosing
- •Has participated in previous clinical trials investigating the ESAT-6 and/or CFP-10 antigens
- •Has a condition which in the opinion of the investigator is not suitable for participation in the trial
- •HIV POSITIVE PARTICIPANTS:
- •Has a confirmed diagnosis of tuberculosis at Screening Visit
- •Has been vaccinated with a live vaccine within 6 weeks prior to the day of inclusion (e.g. MMR, yellow fever, oral typhoid vaccines)
- •Has been tuberculin (TST) tested less than 12 months prior to the day of inclusion
- •Is pregnant, breastfeeding or intending to get pregnant during the trial period
- •Is a female of child bearing potential (12 years of age or older) not willing to use effective barrier (including spermicidal gel), hormonal or intrauterine contraceptive measures during the trial period
- •Has an active disease affecting the lymphoid organs except for HIV (e.g., Hodgkin's disease, lymphoma, leukaemia, sarcoidosis)
- •Has a known diagnosis of AIDS or is receiving antiviral therapy at the time of Screening Visit
- •Has a current skin condition which interferes with the reading of the C-Tb and PPD e.g. tattoos, severe scarring, burns/sunburns, rash, eczema, psoriasis, or any other skin disease at or near the injection sites
- •Has a condition where blood drawings pose more than minimal risk for the participant, such as haemophilia, other coagulation disorders or significantly impaired venous access
- •Currently participating in another clinical trial with an investigational or non-investigational drug or device or has participated in another clinical trial within the 3 months prior to dosing
- •Has participated in previous clinical trials investigating the ESAT-6 and/or CFP-10 antigens
- •Has a condition which in the opinion of the investigator is not suitable for participation in the trial
- •HIV NEGATIVE CONTROL GROUP:
- •Has been vaccinated with a live vaccine within 6 weeks prior to the day of inclusion (e.g. MMR, yellow fever, oral typhoid vaccines) except BCG vaccine
- •Has been tuberculin (TST) tested less than 12 months prior to the day of inclusion
- •Has an active disease affecting the lymphoid organs (e.g., Hodgkin's disease, lymphoma, leukaemia, sarcoidosis)
- •Has a current skin condition which interferes with the reading of the C-Tb and PPD e.g. tattoos, severe scarring, burns/sunburns, rash, eczema, psoriasis, or any other skin disease at or near the injection sites
- •Has a condition where blood drawings pose more than minimal risk for the participant, such as haemophilia, other coagulation disorders, or significantly impaired venous access
- •Currently participating in another clinical trial with an investigational or non-investigational drug or device, or has participated in another clinical trial within the 3 months prior to dosing
- •Has participated in previous clinical trials investigating the ESAT-6 and/or CFP-10 antigens
- •Has a condition which in the opinion of the investigator is not suitable for participation in the trial
研究组 & 干预措施
0.1 µg/0.1 mL C-Tb
The C-Tb and 2 T.U. Tuberculin PPD RT 23 SSI agents are given concomitantly to each volunteer in the RIGHT and LEFT forearms according to a double blind randomisation scheme
干预措施: C-Tb (Biological)
2 T.U. Tuberculin PPD RT 23 SSI
The C-Tb and 2 T.U. Tuberculin PPD RT 23 SSI agents are given concomitantly to each volunteer in the RIGHT and LEFT forearms according to a double blind randomisation scheme
干预措施: 2 T.U. Tuberculin PPD RT 23 SSI (Biological)
结局指标
主要结局
To evaluate the diagnostic performance of C-Tb in relation to age, HIV and CD4 counts
时间窗: Onset between the injections and 28 days after the injections
To evaluate the clinical safety of C-Tb, with emphasis on children and HIV positive participants
时间窗: Onset between the injections and 28 days after the injections
次要结局
- To evaluate the difference in specificity between C-Tb and Tuberculin PPD RT23 SSI in the control group of 100 children aged 5 - 11 years with no TB symptoms and no known exposure to MTb overall, and according to age.(Onset between the injections and 28 days after the injections)
- To compare the diagnostic outcome of C-Tb to that of QuantiFERON®-TB Gold in-Tube using a latent class approach(From injections to 2-3 days after the injections)
- To evaluate the difference in sensitivity between C-Tb and QuantiFERON®-TB Gold in-Tube in trial participants with confirmed TB diagnosis, overall, and according to age and HIV status.(From injections to 2-3 days after the injections)
- To evaluate the difference in sensitivity between C-Tb and Tuberculin PPD RT23 SSI in trial participants with confirmed TB diagnosis overall, and according to age and HIV status.(Onset between the injections and 28 days after the injections)
- To evaluate the difference in specificity between C-Tb and QuantiFERON®-TB Gold in-Tube in the control group of 100 children aged 5 - 11 years with no TB symptoms and no known exposure to MTb overall, and according to age.(From injections to 2-3 days after the injections)
- To compare the diagnostic outcome of C-Tb to that of Tuberculin PPD RT23 SSI using a latent class approach(Onset between the injections and 28 days after the injections)
- To evaluate the diagnostic performance of Tuberculin PPD RT23 SSI in relation to age, HIV status and CD4 counts(Onset between the injections and 28 days after the injections)
- To evaluate the clinical safety of Tuberculin PPD RT23 SSI(Onset between the injections and 28 days after the injections)
- To evaluate the diagnostic performance of QuantiFERON®-TB Gold in-Tube in relation to age, HIV status and CD4 counts(On the day of the injections)