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Phase III Multicenter, Open-Label, Randomized Trial of Induction Versus Induction Plus Maintenance Foscarnet ( Foscavir ) Therapy for Gastrointestinal CMV Disease

Phase III Multicenter, Open-Label, Randomized Trial of Induction Versus Induction Plus Maintenance Foscarnet ( Foscavir ) Therapy for Gastrointestinal CMV Disease

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002145
Enrollment
145
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

Gastrointestinal Diseases, HIV Infections

Keywords

Foscarnet, Cytomegalovirus Infections, Acquired Immunodeficiency Syndrome

Brief summary

PRIMARY: To compare the frequency of and time to relapse of Cytomegalovirus (CMV) gastrointestinal disease following foscarnet induction therapy only versus induction plus maintenance therapy. SECONDARY: To determine frequency of and time to recurrence of gastrointestinal symptoms, response rate of pathological lesions, and incidence of nongastrointestinal CMV disease in this patient population.

Detailed description

Patients receive intravenous foscarnet either as induction only for 4 weeks or as induction for 4 weeks followed by maintenance for 22 weeks. All patients are followed for 26 weeks or until relapse.

Interventions

DRUGFoscarnet sodium

Sponsors

Astra USA
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

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

Inclusion criteria

Patients must have: * AIDS. * CMV GI disease.

Exclusion criteria

Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Non-GI CMV disease. * Ulcerative colitis, inflammatory bowel disease, or other condition that may interfere with study results. * Other GI pathogens. Concurrent Medication: Excluded: * Drugs that may interact with foscarnet. * Systemic acyclovir, ganciclovir, or acyclovir prodrug. * Drugs known to affect renal function. Prior Medication: Excluded: * Prior foscarnet in extremis. * Investigational agents other than 3TC or d4T within 7 days prior to study entry.

Countries

United States

Outcome results

None listed

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