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The Safety and Effectiveness of ISIS 2922 in Patients With AIDS Who Have Cytomegalovirus (CMV) of the Eyes

An Open-Label Study of the Safety and Efficacy of Intravitreal ISIS 2922 in Acquired Immune Deficiency Syndrome (AIDS) Patients With Cytomegalovirus Retinitis (NOTE: Restricted to Patients Who Rollover From Another Controlled ISIS 2922 Trial)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002356
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cytomegalovirus Retinitis, HIV Infections

Keywords

Acquired Immunodeficiency Syndrome, Antiviral Agents, Cytomegalovirus Retinitis

Brief summary

To evaluate the efficacy and safety of ISIS 2922 in AIDS patients with Cytomegalovirus ( CMV ) retinitis who are unresponsive or intolerant to ganciclovir and/or foscarnet but are otherwise ineligible for ISIS Pharmaceuticals' controlled trials OR who have failed ISIS 2922 therapy on another controlled clinical trial. PER 2/8/96 AMENDMENT: Patients must rollover from another ISIS 2922 controlled trial.

Detailed description

Patients receive intravitreal injections of ISIS 2922 at doses of either 150 or 300 mcg, depending on CMV retinitis location and extent of retinal involvement. There is a 3-week Induction period followed by at least 18 weeks of Maintenance. Induction is given on days 1, 8, and 15, and Maintenance doses are given every 14 days, beginning on day 29.

Interventions

Sponsors

Ionis Pharmaceuticals, Inc.
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have: * AIDS. * CMV retinitis in one or both eyes that was previously treated but is presently uncontrolled. * Intolerance or resistance to other therapies.

Exclusion criteria

Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Eligibility to participate in a controlled clinical trial of ISIS 2922. * External ocular infection in eye to be treated. * Other herpetic infections of the retina, toxoplasma retinochoroiditis, or other diseases of the fundus in eye to be treated. * Ocular condition that would obstruct visualization of the posterior ocular structures in eye to be treated. * Retinal detachment in eye to be treated. * Known or suspected allergy to phosphorothioate oligonucleotides. * Silicone oil in eye to be treated. * Syphilis. * Clinical evidence of retinal pigment epithelial stippling. * Pseudoretinitis pigmentosa. Concurrent Medication: Excluded: * Foscarnet. * Mellaril, Stelazine, Thorazine, and Clofazimine. * Ethambutol / fluconazole combination. * Other investigational drugs for CMV retinitis. Patients with the following prior conditions are excluded: * History of surgery to correct retinal detachment in eye to be treated. * History of ganciclovir implant for treatment of CMV retinitis. * History of intolerance to ISIS 2922. * History of syphilis. Required: * Prior CMV retinitis therapy with ganciclovir, foscarnet, or ISIS 2922.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026