This protocol will assess whether HIV infected patients who have received more than one year of hard capsule saquinivir will have an acute decrease in plasma HIV RNA following substitution of this therapy with Indinvir (IDV) or the soft gelatin saquinivir. Other objectives are to assess the nature and duration of plasma RNA over 48 weeks; ascertain whether there are baseline mutations in the protease gene and the extent to which resistance develops; describe CD4 and CD8 changes and to determine safety and tolerablity of these drugs.

Project Start
Project End
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
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