Cytomegalovirus Retinitis, HIV Infections
Conditions
Keywords
Retinitis, AIDS-Related Opportunistic Infections, Drug Therapy, Combination, Foscarnet, Cytomegalovirus Infections, Acquired Immunodeficiency Syndrome, Antiviral Agents, Zidovudine
Brief summary
To evaluate the safety and efficacy of foscarnet induction therapy for treatment of AIDS patients experiencing their first episode of cytomegalovirus (CMV) retinitis. To evaluate the safety and efficacy of three different foscarnet maintenance therapy regimens. To determine the pharmacokinetics of intermittent administration of foscarnet with or without concomitant administration of zidovudine (AZT).
Interventions
DRUGFoscarnet sodium
Sponsors
Astra USA
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Exclusion criteria
Co-existing Condition: Patients with the following are excluded: * Any clinically significant pulmonary or neurologic impairment (e.g., patients who are intubated or comatose). * Corneal, lens, or vitreous opacification which precludes examination of the fundi, or evidence of tuberculotic, diabetic and/or hypertensive retinopathy. * Known allergy to foscarnet. * Recurrent episode of cytomegalovirus (CMV) retinitis. Concurrent Medication: Excluded: * Nephrotoxic drugs. Patients with the following are excluded: * Recurrent episode of cytomegalovirus (CMV) retinitis. * Any clinically significant pulmonary or neurologic impairment (e.g., patients who are intubated or comatose). * Corneal, lens, or vitreous opacification which precludes examination of the fundi, or evidence of tuberculotic, diabetic, and/or hypertensive retinopathy. * Known allergy to foscarnet. Prior Medication: Excluded: * Ganciclovir for cytomegalovirus (CMV) retinitis. * Foscarnet for CMV retinitis. Patients with AIDS as defined by the CDC with manifest first episode cytomegalovirus (CMV) retinitis, as identified by its characteristic ophthalmoscopic appearance and verified by fundus photography. * Patients must be able to give informed consent.
Countries
United States
Outcome results
None listed