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A Study of ISIS 2922 in the Treatment of Advanced Cytomegalovirus Retinitis

Not Applicable
Completed
Conditions
Cytomegalovirus Retinitis
HIV Infections
Registration Number
NCT00002187
Lead Sponsor
Ionis Pharmaceuticals, Inc.
Brief Summary

The purpose of this study is to compare the safety and effectiveness of two dosage schedules for ISIS 2922 in the treatment of advanced cytomegalovirus (CMV) retinitis

Detailed Description

This is a multicenter, prospective, randomized, open-label study comparing 2 dosage schedules of ISIS 2922.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (17)

Retina - Vitreous Associates Med Group

🇺🇸

Los Angeles, California, United States

Novum Inc

🇺🇸

Seattle, Washington, United States

Dr Julio Perez

🇺🇸

Fort Lauderdale, Florida, United States

Univ of Illinois

🇺🇸

Chicago, Illinois, United States

Hahnemann Univ Hosp

🇺🇸

Philadelphia, Pennsylvania, United States

Baylor College of Medicine

🇺🇸

Houston, Texas, United States

Vitreo - Retinal Consultants

🇺🇸

New York, New York, United States

New York Univ Med Ctr

🇺🇸

New York, New York, United States

Indiana Univ Med Ctr

🇺🇸

Indianapolis, Indiana, United States

Duke Univ

🇺🇸

Durham, North Carolina, United States

Univ of California San Francisco / SF Gen Hosp

🇺🇸

San Francisco, California, United States

Dr Jacob Lalezari

🇺🇸

San Francisco, California, United States

Community Eye Med Group

🇺🇸

Pasadena, California, United States

Charlotte Eye Ear Nose & Throat Association

🇺🇸

Charlotte, North Carolina, United States

Georgia Retina

🇺🇸

Atlanta, Georgia, United States

Chicago Ctr for Clinical Research

🇺🇸

Chicago, Illinois, United States

Dr Alan Palestine

🇺🇸

Washington, District of Columbia, United States

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