ACTG 370 - This is a study of Indinavir Sulfate (IDV, Crixivan) combination therapy. Its purpose is to determine the safety, tolerability, immunologic and virologic effects of three treatment regimens IDV will be used in combination with ZDV (zidovudine, AZT), d4T (stavudine, Zerit), DLV (delavirdine, Rescriptor), and/or 3TC (lamivudine, Epivir). The study was developed as a """"""""roll-over"""""""" study for subjects who participated in ACTG 306. The primary objectives of the study are to compare the proportion of subjects in the two ZDV-containing arms who have a plasma HIV RNA concentration below the limit of detection (defined as < 500 copies/ml) at both weeks 20 and 24, and to compare the safety and tolerability of the different treatment regimens.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000046-39S1
Application #
6297373
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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