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Completed Phase 2 Interventional

A Randomized Comparison of Intravitreal ISIS 2922 Plus Ganciclovir Versus Ganciclovir as Treatment for Patients With Cytomegalovirus Retinitis ( CMVR )

ClinicalTrials.gov ID: NCT00002156

Public ClinicalTrials.gov record NCT00002156. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 3:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To determine the clinically safe and effective dose of intravitreal ISIS 2922 alone and as an additive antiviral therapy to ganciclovir in AIDS patients with cytomegalovirus (CMV) retinitis.

Study identification

NCT ID
NCT00002156
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Enrollment
194 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 24, 2005

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Retina - Vitreous Associates Med Group Los Angeles California 90017 —
Community Eye Med Group Pasadena California 911052536 —
San Diego Naval Hosp San Diego California 92134 —
Univ of California San Francisco / SF Gen Hosp San Francisco California 94110 —
Santa Clara Valley Med Ctr San Jose California 95128 —
Univ of Colorado Health Sciences Ctr Denver Colorado 80262 —
Dr Julio Perez Fort Lauderdale Florida 33060 —
Georgia Retina Atlanta Georgia 30327 —
Univ of Illinois Chicago Illinois 60612 —
Indiana Univ Med Ctr Indianapolis Indiana 46202 —
Vitreo - Retinal Consultants New York New York 10028 —
Charlotte Eye Ear Nose and Throat Association Charlotte North Carolina 28204 —
Hahnemann Univ Hosp Philadelphia Pennsylvania 19102 —
Graduate Hosp Philadelphia Pennsylvania 191461192 —
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 752359057 —
Baylor College of Medicine Houston Texas 77030 —
Virginia Eye Consultants Norfolk Virginia 23507 —
Novum Inc Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00002156, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 24, 2005 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00002156 live on ClinicalTrials.gov.

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