Trial record 9 of 30 for:    " July 23, 2008":" August 22, 2008"[FIRST-RECEIVED-DATE]AND HIV[CONDITION]

Genetic Predictors of Raltegravir Penetration Into Cerebrospinal Fluid

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
David Haas, Vanderbilt University
ClinicalTrials.gov Identifier:
NCT00729924
First received: August 4, 2008
Last updated: February 12, 2013
Last verified: February 2013
  Purpose

This study is being done to find out how much of the drug raltegravir (RGV) gets into cerebrospinal fluid (CSF), compared to how much get into the blood and to find out if normal changes in a certain gene in your body affects how much RGV gets into the CSF.


Condition Intervention Phase
HIV Infections
Drug: Raltegravir
Phase 2
Phase 3

Study Type: Interventional
Study Design: Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Official Title: Genetic Predictors of Raltegravir Penetration Into Cerebrospinal Fluid

Resource links provided by NLM:


Further study details as provided by Vanderbilt University:

Primary Outcome Measures:
  • This study will determine if there are associations between a frequent C>T single nucleotide polymorphism (SNP) in the drug transporter gene ABCB1 (also known as MDR1) and penetration of raltegravir (RGV) into cerebrospinal fluid (CSF). [ Time Frame: Day 7 ] [ Designated as safety issue: No ]

Enrollment: 40
Study Start Date: August 2008
Study Completion Date: August 2011
Primary Completion Date: February 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1 Drug: Raltegravir
400mg orally every 12 hours for 7 days
Other Name: MK-0518

Detailed Description:

The multidrug efflux transporter P-glycoprotein (P-gp) is expressed in the blood-brain barrier where it limits entry of substrate drugs into the central nervous system. Raltegravir (MK-0158), a new HIV-1 integrase inhibitor and potentially major addition to the therapeutic armamentarium against HIV, is a substrate for P-gp. Studies are warranted to elucidate the relevance of P-gp transport for raltegravir in the central nervous system.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Able and willing to give written informed consent.
  2. Negative HIV-1 serology documented by any licensed ELISA test kit within 30 days prior to initiating study drug.
  3. Men and women at least 18 but no more than 55 years of age at study entry.
  4. Body mass index less than 30.

    Body mass index = (weight in kilograms)/(height in meters)2 OR Body mass index = [(weight in pounds)/(height in inches)2] X 703

  5. Estimated creatinine clearance ≥ 50 mL/minute within 30 days prior to study entry, calculated by the Cockcroft-Gault method as follows:

    Men: creatinine clearance = [(140 - age) x (weight in kg)]/(72 x serum creatinine)

    Women: creatinine clearance = 0.85 x [(140 - age) x (weight in kg)]/(72 x serum creatinine)

  6. Laboratory values obtained within 30 days prior to study entry:

    • Absolute neutrophil count (ANC) ≥ 1,000/mm3.
    • Hemoglobin ≥ 12.5 g/dL for males and ≥ 11.5 g/dL for females.
    • Platelet count ≥ 100,000/mm3.
    • AST (SGOT), ALT (SGPT), and total bilirubin within normal range.
    • Alkaline phosphatase less than or equal to 1.5 x upper limit of normal (ULN).
  7. Female study volunteers of reproductive potential (defined as women who have not been post-menopausal for at least 24 consecutive months, i.e., who have had menses within the preceding 24 months, or have not undergone surgical sterilization [e.g., hysterectomy, bilateral oophorectomy, or salpingotomy]) must have a negative serum or urine pregnancy test performed within 30 days before study entry.
  8. All study volunteers must agree not to participate in a conception process (e.g., active attempt to become pregnant or to impregnate, sperm donation, in vitro fertilization).

    If participating in sexual activity that could lead to pregnancy, all study volunteers must agree that AT LEAST ONE of the following reliable methods of contraception will be used while they are receiving protocol-specified medications and for 6 weeks after stopping the medications:

    • Condoms1 (male or female) with or without a spermicidal agent
    • Diaphragm or cervical cap with spermicide
    • IUD

      1. Condoms are recommended because their appropriate use is the only contraception method effective for preventing HIV transmission.

    NOTE: Use of hormonal contraceptives is prohibited during this study because of the potential for drug interactions.

    All study volunteers who are not of reproductive potential (e.g., women who have been post-menopausal for at least 24 consecutive months, or women who have undergone surgical sterilization [e.g., hysterectomy and/or bilateral oophorectomy or salpingotomy], or men who have documented azoospermia) are eligible without requiring the use of contraception. Acceptable documentation of sterilization or menopause consists of written or oral documentation communicated by a clinician or a clinician's staff of one of the following:

    • Physician report/letter
    • Operative report or other source documentation in the patient record (a laboratory report of azoospermia is required to document successful vasectomy)
    • Discharge summary
    • Laboratory report of azoospermia
    • FSH measurement elevated into the menopausal range as established by the reporting laboratory.
  9. Drug transporter gene ABCB1 position 3435 genotype either homozygous C/C or homozygous T/T.

Exclusion Criteria:

  1. Within 14 days prior to entry, use of any medication that is metabolized by CYP3A or UGT1A1 (refer to manufacturers' package inserts for individual drugs).
  2. Anticipated need to take any medication that is metabolized by CYP3A or UGT1A1 during the study.
  3. Active drug use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements.
  4. Inability to abstain from alcohol-containing beverages, grapefruit, and grapefruit juice for the duration of the study.
  5. Serious illness that, in the opinion of the investigator, would interfere with study participation.
  6. Hospitalization for any reason or therapy for serious illness within 14 days prior to study entry.
  7. History of hypersensitivity to study drug or its formulation.
  8. As determined by the investigator, a significant active or previous history of cardiovascular, renal, liver, hematologic, neurologic, gastrointestinal, psychiatric, endocrine, or immunologic disease(s). This is inclusive of chronic illnesses such as hypertension, coronary artery disease, arthritis, diabetes, any chronic gastrointestinal conditions that may affect drug absorption, etc.
  9. Breast-feeding.
  10. Evidence of CNS infection or space occupying lesion by history or physical examination.
  11. History of significant CNS disorder such as trauma, congenital malformations or genetic disorders.
  12. Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g., infectious disease) illness must not be enrolled into this study.
  13. ABCB1 position 3435 C/T heterozygosity during screening evaluation.
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00729924

Locations
United States, Tennessee
Vanderbilt Therapeutics Clinical Research Site
Nashville, Tennessee, United States, 37204
Sponsors and Collaborators
Vanderbilt University
Investigators
Principal Investigator: David W Haas, MD Vanderbilt University
  More Information

No publications provided by Vanderbilt University

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: David Haas, Professor of Medicine, Vanderbilt University
ClinicalTrials.gov Identifier: NCT00729924     History of Changes
Other Study ID Numbers: 080536
Study First Received: August 4, 2008
Last Updated: February 12, 2013
Health Authority: United States: Food and Drug Administration
United States: Institutional Review Board

Keywords provided by Vanderbilt University:
Raltegravir
CSF
ABCB1 SNP
HIV/AIDS

Additional relevant MeSH terms:
HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases

ClinicalTrials.gov processed this record on August 19, 2014