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Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States Clinical Trials Info presented on Clinical Trials Search is not intended to be a substitute for certified medical advice, visits or professional assistance using a real physician. We are not physicians. Always consult your dr. about Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States conditions. Clinical Trials Search.org is a site dedicated to listing clinical research studies in human subjects. Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States Clinical research trials and Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States health trials happen in many of localities throughout the U.S.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically measure the effectualness of new drugs. The function of the studies / projects is to resolve particular human medical questions. Clinical trials are a popular manner for mDs, government agencies, and private sector corporations to discover remedies for all varieties of circumstances, like Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States. Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States Clinical Trials and other clinical trials allow volunteers to obtain healthcare treatment options before they are available to the masses. Some times the participants undergo professional assistance for free of charge, and occasionally they are paid for their time. Sometimes there is a cost for a Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States clinical trial. Human subjects often get the best healthcare available for their Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States condition. Dangers are a reality, however, and may include additional or frequent mD visits, healthcare dangers (potentially life-jeopardising), and/or the treatment being ineffectual. Trials are federally governed with rigorous guidelines to protect clinical trials patients.
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Home > "D" Clinical Trials Conditions > Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States  Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States
Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States
For Condition: HIV Infection
Status: Recruiting
Sponsor(s): Warren G Magnuson Clinical Center (CC) ,
Synopsis: 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.
Details: 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.
Eligibility:
Study Type: Interventional, Treatment
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: INCLUSION CRITERIA: 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 X upper limit of normal (ULN) Serum creatinine less than or equal to 2 X 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. EXCLUSION CRITERIA: 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 or equal to 5 X upper limit of normal (ULN) Serum creatinine less than or equal to 2 X ULN Hemoglobin greater than or equal to 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 (less 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.
Total Enrollment: 65
Location and Contact Information:
Warren G. Magnuson Clinical Center (CC) *Recruiting*
Bethesda, Maryland, 20892
United States
Recruiting Patient and Public Liaison Office 1-800-411-1222
Additional Information:
Study ID Numbers: 030091; 03-CC-0091
Study Start Date: February 6, 2003
Record last reviewed: October 3, 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00054743
Other Hiv Infection Studies:
1. Immune Responses to HIV in Blood Cells in HIV-Infected and HIV-Uninfected Volunteers
2. Phase I Study to Evaluate the Safety and Immunogenicity of HIV-1 Immunogen in Children with HIV-1 Infection
3. Safety and Efficacy of Ampligen in the Treatment of HIV Patients Failing HAART
4. Combination Therapy with IL-2 Plus Antiretroviral Drugs to Treat HIV Infection
5. Magnetic Resonance Imaging of the Face and Bones
Related Studies:
Other HIV Infection Clinical Trials
Other Maryland Clinical Trials
Other Bethesda Clinical Trials
Differences in Blood Levels of Nevirapine in HIV-infected Patients in Uganda and the United States
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