DARDAR Health Project (Disseminated Tuberculosis and HIV Infection)
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Enrollment
- 1,975
- Locations
- 1
- Primary Endpoint
- safety and efficacy of a prime-boost immunization strategy for the prevention of HIV-associated dTB and pTB
Study Overview
Brief Summary
A significant number of HIV infected patients in Africa also have disseminated tuberculosis (infection throughout multiple organs). This type of tuberculosis is a significant cause of mortality in these patients. The purpose of this study is to evaluate the safety and effectiveness of a vaccine designed to prevent disseminated tuberculosis.
Detailed Description
Disseminated infection with Mycobacterium tuberculosis (dMTB) has been documented in 10% to 25% of patients with HIV infection in Africa. Unlike pulmonary tuberculosis (pMTB), most cases of dMTB are not recognized and death ensues rapidly. Therefore, dMTB may be a more important cause of HIV-associated mortality than pMTB in developing countries. Mycobacterium vaccae (MV) is an investigational vaccine prepared by heat inactivation of a nontuberculous mycobacteria. MV immunization may reduce the risk of HIV-associated dMTB. The purpose of this study is to define risk factors for HIV-associated dMTB and to assess the safety and effectiveness of an MV vaccine for the prevention of HIV-associated pulmonary and disseminated tuberculosis.
HIV positive patients with prior BCG immunization and HIV negative controls will be entered in a 5-year study in Tanzania. Participants will be randomized to receive a 5-dose series of MV or placebo over 12 months, with a repeat skin test at Month 14. Baseline evaluation will include medical history, chest x-ray, skin tests with purified protein derivative (PPD), and blood tests to evaluate interferon-gamma production. Participants with PPD reactions greater than or equal to 5 mm will receive 6 months of prophylaxis with isoniazid. Participants will be followed every 3 months for 3 to 5 years to assess new pMTB (microbiologic or clinical diagnosis) or dMTB (microbiologic diagnosis). Potential risk factors for dMTB will also be assessed.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •HIV infection
- •CD4 count more than 200 cells/mm3
Exclusion Criteria
- •Active tuberculosis. Patients will be deferred from study enrollment until they show no signs of active disease.
- •Serious underlying disease (e.g., congestive heart failure, advanced cancer)
- •Life expectancy of less than 2 years
- •Pregnancy. Women who are pregnant may be eligible for the study after they give birth.
Arms & Interventions
A
Intervention: SRL-172 (Biological)
B
Intervention: SRL-172 (Biological)
Outcomes
Primary Outcomes
safety and efficacy of a prime-boost immunization strategy for the prevention of HIV-associated dTB and pTB
Time Frame: every six months
Secondary Outcomes
- Risk factors for HIV-associated dTB and relative contributions of primary infection, reinfection, and reactivation in its pathogenesis(every six months)
Investigators
C. Fordham von Reyn
Professor of Medicine
Dartmouth-Hitchcock Medical Center
