70
Participants
Start Date
June 30, 2004
Primary Completion Date
September 30, 2007
Study Completion Date
September 30, 2007
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.
Kilimanjaro Christian Medical Centre, Moshi
Lead Sponsor
Collaborators (1)
Kilimanjaro Christian Medical Centre, Tanzania
OTHER
Kibongoto National Tuberculosis Hospital, Tanzania
UNKNOWN
GlaxoSmithKline
INDUSTRY
Duke University
OTHER