AG 1343 is a well-absorbed inhibitor of HIV-1 protease that has demonstrated potent antiviral activity in vitro and in vivo. This study is designed to continue to test three different dosage schedules of AG 1343 for both activity and safety in those patients who experienced a 90% reduction in viral load during the first 28 days of therapy. Participants will be monitored monthly for evidence of drug efficacy and toxicity. Patients who demonstrate an increase in their viral load while on AG 1343 monotherapy will be allowed to initiate therapy with additional FDA- approved nucleoside analogues.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000102-35S1
Application #
6115863
Study Section
Project Start
Project End
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
35
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Rockefeller University
Department
Type
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
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