The primary objectives of ACTG 365 are to evaluate the safety and tolerability of simultaneous administration of indinavir and rifabutin for 14 days, to evaluate the effects of 1) the simultaneous administration of rifabutin with indinavir for 14 days on the plasma pharmacokinetic profile of refabutin, 2) staggered versus simultaneous administration of indinavir on the PK profile of rifabutin, and 3) simultaneous administration of rifabutin 150 mg and indinavir 1000 mg on the pharmacokinetics of indinavir.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000052-39
Application #
6412321
Study Section
Special Emphasis Panel (ZRR1)
Project Start
1975-10-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
39
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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