Expired Study
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Baltimore, Maryland 21205


Purpose:

To characterize the pharmacokinetics of orally administered FLT (in a liquid formulation) after single doses in both the fed and fasting states; to assess the effect of food on the oral bioavailability of FLT


Criteria:

Inclusion Criteria Patients must have: - Positive ELISA test confirmed by Western blot analysis. - Asymptomatic. - Willing to sign an informed consent. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: - Oral candida infection documented by morphology or by a response to antifungal therapy within two months prior to study entry. - Oral hairy leukoplakia at any time prior to entry. - Temperature > 37.8 C. - Any malignancy other than cutaneous basal cell carcinoma or cervical carcinoma in situ. - Significant chronic underlying medical illness which would prevent continuous participation in this clinical trial. - Unwilling to sign an informed consent. - Zidovudine induced hematological toxicity. Prior Medication: Excluded: - Therapy with antiretroviral drugs or immunomodulators within seven days before entry. - Therapy with any investigational drug during the preceding 30 days. Patients may not have: - Oral candida infection documented by morphology or by a response to antifungal therapy within two months prior to study entry. - Oral hairy leukoplakia at any time prior to entry. - Temperature > 37.8 C. - Any malignancy other than cutaneous basal cell carcinoma or cervical carcinoma in situ. - Significant chronic underlying medical illness which would prevent continuous participation in this clinical trial. - Unwilling to sign an informed consent. - Zidovudine induced hematological toxicity.


NCT ID:

NCT00002260


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21205
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 19, 2017

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