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NCT00002384 Clinical Trial

A Study of Cidofovir in the Treatment of Cytomegalovirus (CMV) of the Eyes in Patients With AIDS

HIV Infections Clinical Trial

Official title:
Vistide (Cidofovir Intravenous) Treatment IND Protocol for Relapsing Cytomegalovirus Retinitis in Patients With AIDS

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00002384
Other study ID # 276A
Secondary ID GS-95-12096ACR-G
Status Active, not recruiting
Phase N/A
First received November 2, 1999
Last updated June 23, 2005

Study information
Verified date August 1997
Source NIH AIDS Clinical Trials Information Service
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Incomplete Closed Protocol

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years and older
Eligibility Information not available

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Cidofovir

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Gilead Sciences Anderson Clinical Research

References & Publications (1)

Stagg RJ, Gathe J, Lieberman RM, Nuessle SJ, Davis JL, Ruane P, Bellman PC, Horgan M, Jaffe HS. The Vistide (cidofovir injection) treatment IND for relapsing CMV retinitis (CMV-R). Conf Retroviruses Opportunistic Infect. 1997 Jan 22-26;4th:120 (abstract no 306)

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