Cytomegalovirus Retinitis, HIV Infections
Conditions
Keywords
Infusions, Intravenous, Ganciclovir, Administration, Oral, Acquired Immunodeficiency Syndrome, Antiviral Agents, Cytomegalovirus Retinitis
Brief summary
To determine whether alternating oral ganciclovir with intravenous ( IV ) ganciclovir can prevent relapse of Cytomegalovirus ( CMV ) retinitis and improve quality of life in AIDS patients. A systemic treatment strategy for CMV retinitis is needed that will be effective yet convenient to administer, without the need for a permanent indwelling IV catheter. Although oral ganciclovir has been used as maintenance following induction with IV ganciclovir, patients with reactivation of disease must be reinduced IV. A fixed-schedule regimen in which oral and IV ganciclovir are alternated may prevent reactivation and progression of disease, as opposed to the current therapeutic strategy in which changes in therapy are event-driven. Also, the duration of intermittent IV therapy required to control disease may be short enough to eliminate the need for an indwelling catheter.
Detailed description
A systemic treatment strategy for CMV retinitis is needed that will be effective yet convenient to administer, without the need for a permanent indwelling IV catheter. Although oral ganciclovir has been used as maintenance following induction with IV ganciclovir, patients with reactivation of disease must be reinduced IV. A fixed-schedule regimen in which oral and IV ganciclovir are alternated may prevent reactivation and progression of disease, as opposed to the current therapeutic strategy in which changes in therapy are event-driven. Also, the duration of intermittent IV therapy required to control disease may be short enough to eliminate the need for an indwelling catheter. Patients receive IV induction with ganciclovir for 2 weeks followed by an alternating course of 3 weeks of oral ganciclovir and 1 week of IV drug for four cycles (16 weeks). If CMV retinitis fails to arrest after initial induction, IV ganciclovir is administered for an additional 2 weeks.
Interventions
DRUGGanciclovir
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Concurrent Medication: Allowed: * Erythropoietin, G-CSF, or GM-CSF. * Antiretrovirals. Patients must have: * HIV infection. * Evaluable CMV retinitis with photographable lesions. * Life expectancy of at least 6 months. * No active AIDS-defining opportunistic infections or malignancies that require nephrotoxic or myelosuppressive therapy.
Exclusion criteria
Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Evidence of retinal vascular or related infectious disease or other retinal lesions that would interfere with the ability to detect responses to therapy or progression. * Corneal, lens, or vitreous opacification precluding funduscopic exam. * Clinically significant pulmonary or neurologic impairment other than seizure disorder or CNS mass lesion. * Inability to obtain temporary IV access. * Requirement for permanent catheters for IV ganciclovir administration. * Uncontrolled diarrhea or nausea preventing ingestion of medicine. * Known hypersensitivity to IV or oral ganciclovir. Concurrent Medication: Excluded: * Immunomodulators. * Biologic response modifiers. * Interferon. * Related investigational agents. * CMV prophylaxis. * Systemic acyclovir. * Any nephrotoxic agent. * Any concomitant therapy that would prohibit use of ganciclovir. Prior Medication: Excluded: * Prior treatment for CMV retinitis. * More than 4 months of prior ganciclovir or foscarnet, or within 4 weeks prior to study entry.
Countries
United States
Outcome results
None listed