Tuberculosis and Human Immunodeficiency Virus (HIV) Immune Reconstitution Syndrome Trial (THIRST)

PHASE4CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

June 30, 2004

Primary Completion Date

September 30, 2007

Study Completion Date

September 30, 2007

Conditions
HIVTuberculosis
Interventions
DRUG

Fixed dose combination zidovudine/lamivudine/abacavir

All subjects will receive fixed dose combination zidovudine(300 mg) / lamivudine (150 mg) / abacavir (300 mg) by mouth twice daily. Medications will be provided as long as deemed beneficial by the site investigator and study subject for up to two years. Toxicity substitutions are allowed per protocol.

Trial Locations (1)

Unknown

Kilimanjaro Christian Medical Centre, Moshi

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Kilimanjaro Christian Medical Centre, Tanzania

OTHER

collaborator

Kibongoto National Tuberculosis Hospital, Tanzania

UNKNOWN

collaborator

GlaxoSmithKline

INDUSTRY

lead

Duke University

OTHER