The is a phase IV clinical trial evaluating two treatment regimens for AIDS-related CMV retinitis, both of which are administered without a central venous catheter: (1) ganciclonir intraocular device plus oral ganciclonir and (2) intravenous cidofovir. The primary objective of the trial is to compare the newest CMV retinitis drug, cidofovir, to a commonly used treatment regimen, the ganciclonir intraocular device plus oral ganciclonir, with respect to efficacy in preventing vision loss. A secondary objective is to compare a treatment regimen that incorporates highly active local therapy with treatments that do not. To accomplish this objective, patients who terminate cidofovir treatment because of toxicity will be recommended to continue with alterative systemic treatment and patients who progress will undergo a second course of induction with cidofovir and will start oral ganciclovir.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000040-40
Application #
6414368
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1974-10-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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