The primary objective of this study is to compare the safety and efficacy of human anti-CMV monoclonal antibody plus active primary treatment vs. matched placebo plus active primary treatment, for both newly diagnosed and relapsed CMV retinitis in patients with AIDS. Study endpoints include change in CMV virologic load and time to progression of retinitis. Additiona outcome measures mortality, change in visual acuity and change in visual fields.

Project Start
1997-01-06
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
37
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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