A Randomized Comparative Pharmacokinetic Study of Oral Ganciclovir After Treatment With Intravenous Ganciclovir for Cytomegalovirus Gastrointestinal Disease in AIDS Patients

• Status: Completed
• Trial end date: 1998-08-01
• Target enrollment: 0
• Participant gender: All

Summary

To determine the oral bioavailability of three dose levels of oral ganciclovir given with and without glutamic acid hydrochloride in patients with cytomegalovirus (CMV) GI disease, and to compare the bioavailability of these regimens to that of standard intravenous (IV) ganciclovir.

Long-term ganciclovir maintenance therapy has been recommended for CMV colitis or esophagitis following induction treatment. Oral ganciclovir is a likely candidate for maintenance because of its possible therapeutic value and ease of administration, but an optimum dose has not been determined. Since oral ganciclovir has a low bioavailability and is more soluble in an acid pH environment, the addition of glutamic acid hydrochloride may enhance gastrointestinal absorption of this drug.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
• Collaborator: Hoffmann-La Roche
• Treatments: Ganciclovir; Ganciclovir triphosphate

Criteria

Inclusion Criteria

Concurrent Medication:

Recommended:

• PCP prophylaxis.

Allowed:

• Antiretroviral therapy during induction and pharmacokinetic part of study, provided patient remains on the same antiretroviral therapy for the duration of the study.

• Chemotherapy for Kaposi's sarcoma, provided patient is hematologically stable for at least 30 days prior to study entry.

• Recombinant human erythropoietin.

• GM-CSF and G-CSF.

• Other medications necessary for patient's welfare, at the physician's discretion.

Patients must have:

• HIV infection.

• Biopsy-proven cytomegalovirus (CMV) colitis.

• Life expectancy of at least 3 months.

• No active AIDS-defining opportunistic infection requiring therapy that is known to cause nephrotoxicity or myelosuppression.

NOTE:

• Kaposi's sarcoma is permitted if patients are hematologically stable for at least 30 days prior to study entry.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

• Other etiologies for diarrhea identified at study entry.

PER AMENDMENT 3/14/95:

• For subjects who have diarrhea - no other etiologies for diarrhea identified within 6 weeks of enrollment.

• Known hypersensitivity to study drugs.

• CMV retinitis.

Concurrent Medication:

Excluded:

• Acyclovir or probenecid (PER AMENDMENT 3/14/95).

• Immunomodulators.

• Biologic response modifiers (other than GM-CSF or G-CSF).

• Investigational agents, with the exception of treatment IND drugs.

• Antacids.

• H2 blockers.

• Proton pump inhibitors.

• Foscarnet during induction and pharmacokinetic part of study.

• Intravenous CMV retinitis maintenance therapy (including ganciclovir) during pharmacokinetic part of study.

• Nephrotoxic agents.

Prior Medication:

Excluded within 14 days prior to study entry:

• Immunomodulators.

• Biologic response modifiers (other than GM-CSF or G-CSF).

• Investigational agents, with the exception of treatment IND drugs.