Studies of Ocular Complications of AIDS (SOCA)--Ganciclovir-Cidofovir CMV Retinitis Trial (GCCRT)

HIV Infections Clinical Trial

— GCCRT  

Official title:

Studies of Ocular Complications of AIDS (SOCA)--Ganciclovir-Cidofovir CMV Retinitis Trial (GCCRT)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00000143
• Other study ID #: NEI-42
• Status: Completed
• Phase: Phase 3
• First received: September 23, 1999
• Last updated: February 18, 2016
• Start date: May 1997
• Est. completion date: June 2000

Study information

• Verified date: July 2015
• Source: Johns Hopkins Bloomberg School of Public Health
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

To compare the newest CMV retinitis drug, cidofovir, with a regimen of the ganciclovir intraocular device plus oral ganciclovir with respect to efficacy in preventing vision loss.

To compare a treatment regimen that incorporates highly active local therapy (ganciclovir device) with a treatment regimen that does not.

Description:

Cytomegalovirus (CMV) is among the most frequently encountered opportunistic infections in patients with AIDS. In the era of prophylaxis for pneumocystic pneumonia, CMV disease is estimated to affect 45 percent of patients with AIDS sometime between the diagnosis of AIDS and death. Retinitis has been estimated to account for up to 85 percent of CMV disease in these patients, making CMV retinitis the most common ocular infection encountered. CMV retinitis is a relatively late-stage manifestation, associated with cluster of differentiation 4 (CD4) + T-cell counts < 100 cells/µL and often < 50 cells/µL.

All currently available treatments for CMV suppress viral replication but do not eliminate the virus from the body. Discontinuation of therapy is associated with a prompt relapse of the retinitis. Despite the use of chronic suppressive therapy, relapse of the retinitis generally occurs, at least with systemically administered anti-CMV drugs.

The first two treatments approved for CMV retinitis were intravenous ganciclovir and intravenous foscarnet. Both are given by daily intravenous infusions and therefore require central venous catheters. The development of newer treatments has focused not only on efficacious treatments, but also on treatments that do not require central venous catheters. Available treatments now include oral ganciclovir, the ganciclovir intraocular device, and intravenous cidofovir.

In vitro data suggest that combination therapies are synergistic in inhibiting viral replication; these therapies include a foscarnet-ganciclovir combination and a cidofovir-ganciclovir combination. In the SOCA--CMV Retinitis Retreatment Trial, the combination of intravenous ganciclovir and foscarnet was more effective than either drug alone for the treatment of relapsed retinitis. Therefore, the combination of intermittent intravenous cidofovir and daily oral ganciclovir may be an attractive therapy for relapsed disease because it may provide synergy for controlling both ocular and visceral disease while not necessitating either a central venous catheter or an intraocular surgical procedure.

The Ganciclovir-Cidofovir CMV Retinitis Trial (GCCRT) is a randomized, multicenter clinical trial. Patients will be assigned to receive one of two regimens: (1) ganciclovir intraocular device plus oral ganciclovir or (2) intravenous cidofovir. The intraocular device will be surgically implanted at baseline and again every 6 to 8 months in eyes with CMV retinitis. Oral ganciclovir is taken at a dose of 1 gram three times daily. Cidofovir will be administered intravenously at 5 mg/kg once weekly for 2 consecutive weeks and once every 2 weeks thereafter. If disease progression occurs in patients receiving cidofovir, patients will be given reinduction therapy, and oral ganciclovir at a dose of 1 gram three times per day will be added to the treatment. If patients assigned to cidofovir are unable to tolerate that regimen, an alternative systemic regimen will be recommended.

Study outcome variables include a decrease of three or more lines from baseline in best corrected visual acuity and rate of visual field loss. The study will also assess other variables including mortality, blood CMV and HIV load, quality of life, and medical costs.

Treatment assignment will not be masked to either patients or clinicians; however, reading of fundus photographs to determine both change in retinal involvement and progression will be masked.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: June 2000
• Est. primary completion date: June 2000
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 13 Years and older

Eligibility

Inclusion criteria:

• Age 13 years or older

• Diagnosis of AIDS according to current Centers for Disease Control and Prevention (CDC) definition

• Diagnosis of active CMV retinitis by a SOCA-certified ophthalmologist (involvement of any zone or amount of retina is allowed)

• Best corrected visual acuity of 20/100 or better in at least one eye

• At least one lesion 750 cells/µL or greater

• Platelet count 50,000 cells/µL or greater

• Willingness and ability, with the assistance of a caregiver if necessary to comply with treatment and follow up procedures

• Willingness of all men and women of childbearing potential to practice adequate birth control to prevent pregnancies during the study and for 3 months afterwards

• Collection of all baseline data within 5 days prior to randomization

• Signed consent statement

Exclusion criteria:

• Media opacities that preclude visualization of the fundus of all otherwise eligible eyes

• Treatment for CMV retinitis with the ganciclovir intraocular implant within 9 months of study entry

• Medical problems or drug or alcohol abuse sufficient to hinder adherence to treatment or follow up procedures

• Unwillingness to refrain from breast-feeding during the study and for 3 months afterwards

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cytomegalovirus Retinitis
• HIV Infections
• Retinitis

Intervention

Device:
• Ganciclovir implant and oral ganciclovir
oral ganciclovir, 1 gm three times daily

Drug:
• Cidofovir intravenous
intravenous, 5 mg/kg once weekly for two doses, followed by 5 mg/kg every other week

Locations

Country	Name	City	State
United States	The Emory Clinic, Emory University	Atlanta	Georgia
United States	The Wilmer Ophthalmological Institute, The Johns Hopkins University School of Medicine	Baltimore	Maryland
United States	Harvard/BCH AIDS Clinical Trials Unit, Massachusetts General Hospital	Boston	Massachusetts
United States	University of North Carolina at Chapel Hill	Chapel Hill	North Carolina
United States	Department of Ophthalmology, Northwestern University	Chicago	Illinois
United States	Cullen Eye Institute, Baylor College of Medicine	Houston	Texas
United States	Division of Infectious Diseases, Indiana University, Indianapolis	Indianapolis	Indiana
United States	Department of Ophthalmology, University of California, Irvine	Irvine	California
United States	Shiley Eye Center Center, 0946, University of California, San Diego	La Jolla	California
United States	Jules Stein Eye Institute, University of California, Los Angeles	Los Angeles	California
United States	LAC/USC Medical Center, 5P21 Rand Schrader Clinic	Los Angeles	California
United States	Bascom Palmer Eye Institute, University of Miami	Miami	Florida
United States	LSU Eye Center, Louisiana State University Medical Center	New Orleans	Louisiana
United States	Department of Ophthalmology, Mount Sinai School of Medicine	New York	New York
United States	Department of Ophthalmology, New York Hospital-Cornell Medical Center	New York	New York
United States	Department of Ophthalmology, New York University Medical Center	New York	New York
United States	UMDNJ-New Jersey Medical School	Newark	New Jersey
United States	Beckman Vision Center, University of California, San Francisco	San Francisco	California
United States	University of South Florida, MDC Box 21	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Johns Hopkins Bloomberg School of Public Health

Country where clinical trial is conducted

United States, 

References & Publications (2)

Dunn JP, Van Natta M, Foster G, Kuppermann BD, Martin DF, Zong A, Jabs DA; Studies of Ocular Complications of AIDS Research Group. Complications of ganciclovir implant surgery in patients with cytomegalovirus retinitis: the Ganciclovir Cidofovir Cytomegalovirus Retinitis Trial. Retina. 2004 Feb;24(1):41-50. — View Citation

Studies of Ocular Complications of AIDS Research Group. The AIDS Clinical Trials Group.. The ganciclovir implant plus oral ganciclovir versus parenteral cidofovir for the treatment of cytomegalovirus retinitis in patients with acquired immunodeficiency syndrome: The Ganciclovir Cidofovir Cytomegalovirus Retinitis Trial. Am J Ophthalmol. 2001 Apr;131(4):457-67. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Survival		3 years	Yes

External Links

•   Other Studies of the Ocular Complications of AIDS (SOCA)]