This is a 48 week, open-label, randomized, multicenter, efficacy, and safety study. A total of 300 patients will be randomly allocated to one of two treatment regimens ( 100 in Treat A and 200 in Treatment B,1:2 ratio): :Continued therapy with current PI(s)+ two NRTIs or two PIs + two NTRI regimen (treatment A) :Efavirenz (600 mg orally QD)+continued therapy with two NRTIs (Treatment B)-see glossary for abbreviation The PI(s) and NTRI medication will not be supplied by sponsor for Treatment A, the NTRI and PI(s) will remain the same as those administered prior to study entry and will be the patient's first effective HIV protease Inhibitor-containing regimen. For Treatment B, patients randomized to efavirenz.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000750-28
Application #
6411919
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1976-12-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
28
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
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