The primary objective of this study is to examine the safety and immune responses elicited by combining MN rgp120 or bivalent AIDSVAX B/E vaccine with the adjuvant QS-21. The safety of the two expermental vaccines will be assessed when formulated with QS-21 or QS-21 plus alum. In particular, the study will address whether the new preparation of QS-21 in polysorbate 80 is less reactogenic than the QS-21 formulation used in AVEG Protocols.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000095-39S2
Application #
6264589
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
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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