This prospectively randomized, controlled study will substantiate the efficacy of intravenous ganciclovir for the treatment of peripheral cytomegalovirus (CMV) retinitis in patients with AIDS, as measured by changes in retinal lesions/inflammation as the primary endpoint. It will also determine in this patient population the safety of and the overall clinical response to a 16-week course of intravenous ganciclovir therapy.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000096-30A1
Application #
3863976
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
30
Fiscal Year
1991
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
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