NCT Number: NCT00002169
A Study of Viracept in AIDS Patients With Cytomegalovirus Retinitis
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.
Looking for future studies?
Notify MeKey information
Conditions
Age range
13 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Univ of Southern California / LA County USC Med Cntr, Los Angeles, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Agouron Pharmaceuticals
Industry
Registry information
Official study 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
Important dates
- First posted
- Aug 31, 2001
- Registry last updated
- Jun 24, 2005
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
A Study of Foscarnet Plus Ganciclovir in the Treatment of Cytomegalovirus of the Eye in Patients With AIDS Who Have Already Been Treated With Ganciclovir
NCT00000970
AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome
Los Angeles, California, United States
View Trial DetailsFoscarnet Treatment of Serious CMV Retinitis Infection in Patients With Acquired Immunodeficiency Syndrome
NCT00000726
AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome
Los Angeles, California, United States
View Trial DetailsA Phase II Dose-Ranging, Open-Labelled Trial of Foscarnet Salvage Therapy for AIDS Patients With Sight-Threatening CMV Retinitis Who Cannot Be Treated With Ganciclovir Due To Myelosuppression or Treatment Failure
NCT00000691
AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome
Los Angeles, California, United States
View Trial DetailsA Phase I Pharmacokinetic and Tolerance Study of 28-Day Regimens of Oral Ganciclovir
NCT00000668
AIDS-Related Opportunistic Infections, Acquired Immunodeficiency Syndrome
San Diego, California, United States
View Trial Details