Pharmacokinetics of Total Phosphorylated Zidovudine in Mononuclear Cells From HIV-Infected Patients
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 20
- Locations
- 1
Study Overview
Brief Summary
To define the pharmacokinetic parameters (blood levels) of total phosphorylated zidovudine (AZT) in peripheral blood mononuclear cells (PBMC) from HIV-infected patients.
Despite an understanding of the serum (or plasma) pharmacokinetics (blood levels) of AZT, a therapeutic concentration range and optimal dosing interval have not yet been determined.
Detailed Description
Despite an understanding of the serum (or plasma) pharmacokinetics (blood levels) of AZT, a therapeutic concentration range and optimal dosing interval have not yet been determined.
Three studies are planned on two separate patient groups. Group (1) Patients who have never taken AZT start on a standard dose of AZT. Blood samples are taken hourly for an 8-hour period on days 1 and 14. Other blood samples are taken on days 2, 4, and 8. Group (2) Patients who have never taken AZT are given a standard dose for the first week, increasing each week until week 5. Blood samples are taken at the end of each weekly treatment. After 4 weeks of standard treatment, patients in groups 1 and 2 return and receive a single morning dose of oral AZT. Blood samples are taken immediately before dosing and at 1, 2, 4, 6, and 8 hours after dosing. After a 48-hour clearance period, patients return and resume dosing. Blood samples are again taken over an 8-hour period. After 24 weeks of standard treatment, the pharmacokinetic studies are repeated.
Study Design
- Study Type
- Interventional
- Primary Purpose
- Treatment
Eligibility Criteria
- Ages
- 13 Years to — (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Concurrent Medication:
- •FDA-approved anti-pneumocystis and antifungal prophylactic or suppressive regimens.
- •Acyclovir for up to 3 weeks intermittently.
- •Patients must:
- •Meet current guidelines for receiving prescription zidovudine.
- •Have written informed consent from both subject and parent or guardian if under
- •Be capable of understanding and giving informed consent. Women and minorities are actively encouraged to participate.
Exclusion Criteria
- •Co-existing Condition:
- •Patients with the following conditions or symptoms are excluded:
- •Malabsorption syndrome (3 or more loose stools/day for at least 4 weeks associated with unintentional weight loss of greater than 10 percent of body weight).
- •Concurrent Medication:
- •Probenecid or non-FDA approved investigational drugs.
- •Systemic chemotherapy.
- •Other antiviral agents, licensed or investigational, including ganciclovir, foscarnet, ribavirin, didanosine (ddI), dideoxycytidine (ddC), and dideoxydidehydrothymidine (D4T).
- •Chronic acyclovir.
- •Patients with the following are excluded:
- •Active bacterial, fungal, or viral infection requiring systemic therapy not specifically allowed.
- •Significant, chronic medical conditions that could impair compliance with study treatment.
- •Prior Medication:
- •Zidovudine (AZT).
- •Systemic chemotherapy within previous 6 months.
- •Acyclovir within 30 days of study entry.
- •Risk Behavior:
- •Unable to take oral medication reliably.
- •Alcohol or drug abuse that could impair compliance with study treatment.