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Influence of Probenecid and Quinine on the Pharmacokinetics of Azidothymidine

Influence of Probenecid and Quinine on the Pharmacokinetics of Azidothymidine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000706
Enrollment
12
Registered
2001-08-31
Start date
Unknown
Completion date
1988-12-31
Last updated
2021-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Quinine, Probenecid, Drug Therapy, Combination, Acquired Immunodeficiency Syndrome, AIDS-Related Complex, Zidovudine

Brief summary

Part I studies the effect of quinine on how zidovudine (AZT) is used by the body and eliminated through the kidneys in HIV infected patients. Part II studies the effect of probenecid and quinine on the same aspects. Because AZT leaves the bloodstream quickly, patients must take the drug frequently to keep adequate amounts in their bodies. Probenecid and quinine may slow down the rate at which AZT leaves the body. Therefore, taking these drugs along with AZT may reduce the amount of AZT needed for treatment.

Detailed description

Because AZT leaves the bloodstream quickly, patients must take the drug frequently to keep adequate amounts in their bodies. Probenecid and quinine may slow down the rate at which AZT leaves the body. Therefore, taking these drugs along with AZT may reduce the amount of AZT needed for treatment. In part I, four patients who are now receiving AZT at the usual dose take part in pharmacokinetic studies (how much of the drug enters the blood stream, what happens to the drug in the body, and how it leaves the body) of AZT defined after a dose while at steady state and then again after a new steady state has been reached following the addition of quinine sulfate. Part II studies the pharmacokinetics of AZT in eight patients receiving AZT at 1 of 2 doses and then at the lower dose of AZT plus probenecid with or without quinine.

Interventions

DRUGProbenecid
DRUGZidovudine

Sponsors

National Institute of Allergy and Infectious Diseases (NIAID)
Lead SponsorNIH

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

Patients must: * Have symptomatic HIV infection. * Be taking zidovudine (AZT), 100 or 200 mg, 5 or 6 x/day. Allowed: * History of Pneumocystis carinii pneumonia (PCP). * Advanced AIDS related complex (ARC). * HIV antibody positive with an absolute CD4 lymphocyte count of \< 200 cells/mm3 before study entry.

Exclusion criteria

Co-existing Condition: Patients with any of the following conditions are excluded: * Glucose-6-phosphate dehydrogenase deficiency. * Allergy to sulfa drugs, probenecid, or quinine. Concurrent Medication: Excluded: \- Other drugs that might influence the metabolism or renal excretion of zidovudine (AZT).

Countries

United States

Outcome results

None listed

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