A Multicenter, Open-Label, Randomized, 24-Week Study to Compare the Safety and Activity of Indinavir Sulfate, 800 Mg q 8 h Versus 1,200 Mg q 12 h in Combination With Zidovudine and 3TC

PHASE3CompletedINTERVENTIONAL
Enrollment

400

Participants

Timeline

Start Date

Not specified

Conditions
HIV Infections
Interventions
DRUG

Indinavir sulfate

DRUG

Lamivudine

DRUG

Stavudine

DRUG

Zidovudine

Trial Locations (15)

15261

Pittsburgh Treatment Ctr / Univ of Pittsburgh, Pittsburgh

19129

Allegheny Univ Hosp, Philadelphia

19899

Wilmington Hosp / Med Ctr of Delaware, Wilmington

20007

Georgetown Univ Med Ctr, Washington D.C.

21287

Johns Hopkins Hosp, Baltimore

30308

AIDS Research Consortium of Atlanta, Atlanta

60612

Cook County Hosp, Chicago

63108

Washington Univ, St Louis

90033

LAC/USC Med Ctr, Los Angeles

94110

Kaiser Med Ctr, San Francisco

98104

Univ of Washington / AIDS Clinical Trial Unit, Seattle

117948153

Univ Hosp / SUNY at Stony Brook / AIDS TMT Unit, Stony Brook

352942050

Univ of Alabama at Birmingham, Birmingham

372321302

Vanderbilt Univ Med Ctr, Nashville

02906

Brown Univ / Miriam Hosp, Providence

All Listed Sponsors
lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00002208 - A Multicenter, Open-Label, Randomized, 24-Week Study to Compare the Safety and Activity of Indinavir Sulfate, 800 Mg q 8 h Versus 1,200 Mg q 12 h in Combination With Zidovudine and 3TC | Biotech Hunter | Biotech Hunter