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Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00054743
Recruitment Status : Completed
First Posted : February 10, 2003
Last Update Posted : July 2, 2017
Information provided by:
National Institutes of Health Clinical Center (CC)

Brief Summary:

This study will determine whether blood levels of the anti-HIV medicine nevirapine are different in HIV-infected patients in the United States from patients in Uganda. People from all over the world take medications to treat HIV infection. These medicines work well in some people but not in others, and they cause harmful side effects in some people and not in others. These differences may be related to variations in how much of the drug reaches the blood. Differences in drug blood levels among people in various areas of the world may be attributed to differences in diet, state of health, ability to absorb the medicines from the stomach, ability to eliminate the drugs from the body, and the brand of medicine taken. This study will help scientists learn whether differences in blood levels of HIV medicines are important in determining how well the drugs work in different patient populations.

HIV-infected patients 18 years of age and older in the United States and in Kampala, Uganda who have been on an antiretroviral treatment regimen that includes at least 28 consecutive days of nevirapine may be eligible for this study. Candidates will be screened with a medical history, physical examination, and blood tests.

Participants will have a total of approximately about 5 ounces of blood drawn during this 6- to 8-hour study. They will come to the NIH clinic in the morning, and a catheter (plastic tube) will be inserted into an arm vein for collecting blood. (Alternatively, blood can be collected by a needle inserted into an arm vein.) Blood will be withdrawn according to the following schedule:

  • About 5 tablespoons will be collected upon arrival at the clinic after an overnight fast. Within 30 minutes of this blood draw, the patient will have breakfast and take his or her morning dose of nevirapine, along with any other medications that need to be taken at that time.
  • 1 tablespoon of blood will be drawn 2 hours after the nevirapine dose.
  • 1 tablespoon of blood will be drawn 4 hours later (6 hours after the nevirapine dose).

The blood will be analyzed for levels of nevirapine and possibly other HIV medicines. Some of the blood will be stored for later analysis of genes (cytochrome P450 and MDR1) that are involved in eliminating medicines from the body.


Condition or disease Intervention/treatment Phase
HIV Infection Procedure: Blood draw Phase 4

Detailed Description:
The overwhelming majority of HIV-infected persons reside in the developing world. As such, recent efforts have focused on providing antiretroviral pharmacotherapy to this population. However, there are a number of factors indigenous to non-Western HIV-infected patients that may alter their virologic, immunologic, and/or toxicologic response to antiretroviral therapy. Absorption, distribution, and clearance of antiretroviral medications may differ among patients residing in non-Western countries secondary to dietary influences, parasitic infection, and malabsorption. Genetic polymorphisms of drug metabolizing enzymes (cytochrome P450; CYP) and drug transporters (i.e. P-glycoprotein) may also contribute to altered pharmacokinetics among these patients. The purpose of this pilot, hypothesis-generating study is (1) to characterize the pharmacokinetics of the non-nucleoside reverse transcriptase inhibitor nevirapine in a non-Western HIV-infected population (Kampala, Uganda) and in a similar cohort of HIV-infected individuals in the United States and (2) to compare pharmacokinetic parameter values between the groups. Twenty-five subjects from each site will participate. Subjects from the Ugandan site may participate regardless of their CD4+ lymphocyte count and viral load; they will be studied prior to the U.S. cohort. The U.S. group will be selected to include subjects that are matched by gender to their Ugandan counterparts. Subjects will have one pre-dose and two post-dose blood samples collected for the determination of nevirapine plasma concentrations. Samples will be analyzed using LC/MS-MS. Population pharmacokinetics parameter values (Cmax, Cmin, AUC, CL/F, Vd) will be determined using NONMEM(Trademark) and compared between groups. Blood samples collected during the study will also be used to determine CYP and MDR1 genotypes of study subjects in an effort to explain any observed differences in pharmacokinetics parameter values between the study populations.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 24 participants
Primary Purpose: Treatment
Official Title: Global Initiative to Characterize Differences in Antiretroviral Pharmacokinetics in HIV-Infected Populations
Study Start Date : February 6, 2003
Actual Study Completion Date : April 28, 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

    1. Documentation in the patient's medical record of HIV-1 infection using double ELISA or a second confirmatory test (e.g., Western Blot) or any one of the following: detectable p24 antigen, quantifiable plasma HIV RNA, or detectable proviral DNA.
    2. Males and females greater than or equal to 18 years of age
    3. Laboratory values within acceptable limits

      AST/SGOT less than or equal to 5 times the upper limit of normal (ULN)

      Serum creatinine less than or equal to 2 times the ULN

      Hemoglobin greater than or equal to 9.0 g/dL

    4. Receipt of a stable nevirapine-containing antiretroviral regimen for at least 28 days.
    5. Informed consent signed and subject declares that they have been adherent to their nevirapine-containing antiretroviral regimen.


  1. Presence of life-threatening or unstable renal, hepatic, cardiovascular, hematologic, neurologic, psychiatric, or respiratory disease, as determined by medical records, or any other condition that may interfere with the interpretation of the study results or not be in the best interest of the subject in the opinion of the investigator.
  2. Laboratory values outside acceptable limits

    AST/SGOT less than 5 times the upper limit of normal (ULN)

    Serum creatinine greater than 2 times the ULN

    Hemoglobin less than 9.0 g/dL

  3. Positive pregnancy test.
  4. Receipt of IL-2 within 3 months of study participation.
  5. Drug or alcohol use that may impair safety or adherence.
  6. Poor venous access.
  7. Documented or reported fever (greater than 38.5 degrees C) within 7 days of screening.
  8. Active opportunistic infection requiring therapy.
  9. Refusal to agree to allow for specimens to be stored for future research.
  10. Greater than 4 loose/soft stools per day.
  11. Subject is non-adherent with their nevirapine-containing antiretroviral regimen and/or they have not provided informed consent.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00054743

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United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892
Joint Clinical Research Center (JCRC)
Kampala, Uganda
Sponsors and Collaborators
National Institutes of Health Clinical Center (CC)

Layout table for additonal information Identifier: NCT00054743    
Other Study ID Numbers: 030091
First Posted: February 10, 2003    Key Record Dates
Last Update Posted: July 2, 2017
Last Verified: April 28, 2011
Keywords provided by National Institutes of Health Clinical Center (CC):
Cytochrome P450
Population Pharmacokinetics
Additional relevant MeSH terms:
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HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases