Skip to main content
Clinical Trials/NCT00052195
NCT00052195CompletedPhase 2

DARDAR Health Project (Disseminated Tuberculosis and HIV Infection)

Dartmouth-Hitchcock Medical Center1 site in 1 country1,975 target enrollmentStarted: September 1, 2001Last updated:
Conditions
Interventions

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

Experimental

Intervention: SRL-172 (Biological)

B

Placebo Comparator

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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

C. Fordham von Reyn

Professor of Medicine

Dartmouth-Hitchcock Medical Center

Study Sites (1)

Loading locations...

Similar Trials

Investigational Vaccine for the Prevention... | Clinical Trial