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Last Updated: October 20, 2019

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CLINICAL TRIALS PROFILE FOR CYTOVENE

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Clinical Trials for Cytovene

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed Baylor College of Medicine Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed Icahn School of Medicine at Mount Sinai Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed Johns Hopkins University Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed Memorial Sloan Kettering Cancer Center Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed National Eye Institute (NEI) Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
NCT00000134 Studies of the Ocular Complications of AIDS (SOCA)--Cytomegalovirus Retinitis Retreatment Trial (CRRT) Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 3 1992-12-01 To compare the relative merits of three therapeutic regimens in patients with AIDS and CMV retinitis who have been previously treated but whose retinitis either is nonresponsive or has relapsed. These three therapeutic regimens were (1) foscarnet, (2) high-dose ganciclovir, and (3) combination foscarnet and ganciclovir. To compare two treatment strategies in patients with relapsed or nonresponsive CMV retinitis: (1) continuing the same anti-CMV drug or (2) switching to the alternate drug.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Cytovene

Condition Name

Condition Name for Cytovene
Intervention Trials
HIV Infections 5
Cytomegalovirus Retinitis 4
Liver Transplantation 1
CMV Cytomegalovirus Retinitis 1
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Condition MeSH

Condition MeSH for Cytovene
Intervention Trials
Cytomegalovirus Retinitis 5
Retinitis 5
HIV Infections 5
Neoplasms 1
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Clinical Trial Locations for Cytovene

Trials by Country

Trials by Country for Cytovene
Location Trials
United States 10
Canada 1
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Trials by US State

Trials by US State for Cytovene
Location Trials
California 2
New York 1
Georgia 1
Florida 1
Alabama 1
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Clinical Trial Progress for Cytovene

Clinical Trial Phase

Clinical Trial Phase for Cytovene
Clinical Trial Phase Trials
Phase 3 2
Phase 2/Phase 3 2
Phase 1 2
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Clinical Trial Status

Clinical Trial Status for Cytovene
Clinical Trial Phase Trials
Completed 6
Recruiting 1
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Clinical Trial Sponsors for Cytovene

Sponsor Name

Sponsor Name for Cytovene
Sponsor Trials
Johns Hopkins Bloomberg School of Public Health 4
Icahn School of Medicine at Mount Sinai 3
University of Miami 3
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Sponsor Type

Sponsor Type for Cytovene
Sponsor Trials
Other 45
NIH 5
Industry 1
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