Expired Study
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Wallingford, Connecticut 06492


Purpose:

To provide oral sorivudine ( BV-araU ) to pediatric HIV-infected patients with varicella-zoster viral disease who have failed or are intolerant of alternative therapy.


Study summary:

Any physician qualified to treat pediatric AIDS patients may enroll patients in this study.


Criteria:

Inclusion Criteria Patients must have: - HIV infection. - Cutaneous, visceral, or ocular varicella-zoster viral infection. - Refractory or intolerant to acyclovir or foscarnet therapy. - Consent of parent or guardian. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: - Inability to take oral capsules or tolerate liquids. Concurrent Medication: Excluded: - 5-flucytosine, 5-fluorouracil, high-dose prednisone, or probenecid. Patients with the following prior condition are excluded: History of immediate hypersensitivity to nucleoside analogues. Prior Medication: Excluded: - 5-flucytosine, 5-fluorouracil, high-dose prednisone, or probenecid within 4 weeks prior to study entry. Required: - Prior acyclovir or foscarnet.


NCT ID:

NCT00002358


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Wallingford, Connecticut 06492
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 20, 2017

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