This trial was developed to determine the safety and tolerance of three possible dosage levels of a human anti-cytomegalovirus antibody when administered once every two weeks during the maintenance phase of DHPG therapy to patients with AIDS and documented evidence of CMV retinitis. It is required the DHPG pharmacokinetics be performed at dose 1.

Project Start
Project End
Budget Start
Budget End
Support Year
31
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Type
DUNS #
041367053
City
Galveston
State
TX
Country
United States
Zip Code
77555
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