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NCT00002169 Clinical Trial

A Study of Viracept in AIDS Patients With Cytomegalovirus Retinitis

HIV Infections Clinical Trial

Official title:
A Phase II, Randomized, Placebo-Controlled Study to Determine the Effects of Viracept on the Clinical Outcome of Cytomegalovirus (CMV) Retinitis in AIDS Patients Who Are Receiving Standard Induction and Maintenance Therapy for This Infection

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00002169
Other study ID # 259A
Secondary ID Study 517AG1343-
Status Completed
Phase Phase 2
First received November 2, 1999
Last updated June 23, 2005

Study information
Verified date May 1999
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

The purpose of this study is to see if it is safe and effective to give Viracept to AIDS patients who are already being treated for cytomegalovirus (CMV) retinitis.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years and older
Eligibility Inclusion Criteria

Patients must have:

- HIV infection.

- Newly diagnosed or first progression of CMV retinitis.

Exclusion Criteria

Prior Medication:

Excluded:

Prior therapy (or less than 2 weeks) with protease inhibitor other than saquinavir.

Study Design

Endpoint Classification: Safety Study, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Nelfinavir mesylate

Locations
Country Name City State
United States Northwestern Univ / SOCA Chicago Illinois
United States Univ of Texas Med Branch Galveston Texas
United States Baylor Univ Houston Texas
United States Univ of Southern California / LA County USC Med Cntr Los Angeles California
United States Univ of California / UCI Med Ctr Orange California
United States Univ of California / San Diego Treatment Ctr San Diego California
United States Harbor UCLA Med Ctr Torrance California
United States George Washington Univ Washington District of Columbia

Sponsors (1)
Lead Sponsor Collaborator
Agouron Pharmaceuticals

Country where clinical trial is conducted

United States, 

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