Trial record 5 of 67 for:    hypercoagulation OR thrombophilia OR blood clotting | Open Studies | NIH, U.S. Fed

The Interaction of Two HIV Medications With Blood Clot Medications in Healthy Volunteers

This study is currently recruiting participants. (see Contacts and Locations)
Verified April 2014 by National Institutes of Health Clinical Center (CC)
Sponsor:
Collaborator:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:
NCT01896622
First received: July 6, 2013
Last updated: August 1, 2014
Last verified: April 2014
  Purpose

Background:

- People who have the human immunodeficiency virus (HIV) often take several medications to control their disease. They may also need to take medicine to prevent blood clots. Taking both kinds of medicine together can cause bleeding or other problems. But this might not happen if the medications are taken at different times. Researchers will study two particular HIV drugs (ritonavir and cobicistat) and how they interact with blood clot medications.

Objectives:

-To understand how HIV medicine and blood clot medicine interact, so doctors can choose what to prescribe for people who take both.

Eligibility:

- Healthy adults between 18 and 70 years old who are not on any medications.

Design:

  • Participants will be screened with a physical exam and medical history. Blood samples will be collected. Urine samples will be collected from participants who might become pregnant.
  • Participants will visit the National Institutes of Health 7 times after the screening visit. Three visits will last about 12 hours. The other 4 will last about 1 hour.
  • Participants will take a daily dose of either study medication for 22 days. They will keep a diary of medicine they take and any side effects.
  • Treatment will be monitored with blood tests over about 2 months.
  • When the study of one drug is completed, the next drug study will begin with a different group of participants.

Condition Intervention Phase
HIV
Drug: Ritonavir
Drug: Cobicistat
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Pharmacokinetics/Dynamics Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Influence of Cobicistat or Ritonavir on Dabigatran Pharmacokinetics and Pharmacodynamics in Healthy Volunteers

Resource links provided by NLM:


Further study details as provided by National Institutes of Health Clinical Center (CC):

Primary Outcome Measures:
  • To characterize dabigatran pharmacokinetics alone and in combination with ritonavir or cobicistat, respectively, using 2 different dosing strategies, in healthy volunteers. [ Time Frame: Days 0-1, Days 19-20, Days 26-27 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • To characterize dabigatran pharmacodynamics (as measured by ECT) alone and in combination with RTV or COBI, respectively, using 2 different dosing strategies in healthy volunteers [ Time Frame: Days 0-1, Days 19-20, Days 26-27 ] [ Designated as safety issue: No ]

Estimated Enrollment: 50
Study Start Date: June 2013
Estimated Study Completion Date: May 2015
Estimated Primary Completion Date: May 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A
Ritonavir
Drug: Ritonavir
Impact on dabigatran PK/PD
Experimental: B
Cobicistat
Drug: Cobicistat
Impact on dabigatran PK/PD

Detailed Description:

Advances in antiretroviral (ARV) pharmacotherapy have translated to increased longevity and improved quality of life in people living with HIV; hence, elderly individuals comprise an increasing proportion of today s HIV population. Moreover, HIV infection itself has become recognized as a condition characterized by a hypercoaguable state and premature immunologic aging. Potential interactions between ARVs and anticoagulant medications are of particular concern considering that many elderly, and even non-elderly HIV patients will require short-term or chronic anticoagulation to prevent and/or treat systemic embolism. Dabigatran, administered as dabigatran etexilate, is an oral irreversible, competitive direct thrombin inhibitor, which has been shown to be superior to warfarin, and non-inferior to enoxaparin, in preventing thromboembolism in patients with atrial fibrillation and undergoing orthopedic surgery, respectively.

While dabigatran itself is not a substrate of Permeability-glycoprotein (P-gp), its inactivepro-drug, dabigatran etexilate, is a substrate of P-gp. Co-administration of dabigatran etexilate with P-gp modulators has resulted in significant changes in dabigatran exposure. The pharmacokinetic enhancers, ritonavir and cobicistat, as inhibitors of P-gp, are expected to increase plasma concentrations of dabigatran; however, neither agent has been studied in combination with dabigatran etexilate, to date. Hence, the purpose of this study is to determine whether the separate co-administration of ritonavir or cobicistat with dabigatran etexilate increases the systemic exposure of dabigatran in healthy volunteers, and if so, whether adjusting the administration times of these medications can circumvent this interaction.

In this open-label study, 32 healthy volunteers will be assigned to 1 of 2 groups. Group A will consist of 16 subjects who will take 22 days of ritonavir; Group B will consist of 16 subjects who will take 22 days of cobicistat. All subjects will receive 3 separated single doses of dabigatran etexilate. Pharmacokinetic (PK) and pharmacodynamics (PD) sampling for dabigatran will occur on Days 0 1, Day 19 1 20, and Day 26 1 27.

The PD effects of dabigatran will be characterized via ecarin clotting time (ECT) measurements. Dabigatran PK/PD parameters will be determined using non-compartmental methods with the WinNonlin professional computer program (version 5.2; Pharsight Corporation, Mountain View, CA). The following PK/PD parameters will be compared between the groups: area under the curve from 0 to 24 hours (AUC0-24), maximum total dabigatran plasma concentration (Cmax), area under the curve from 0 to infinity hours (AUC0- ), time to maximum plasma concentration (tmax), terminal half-life (T (Omega)), apparent oral clearance (CL/F), area under the effect curve from 0 to 24 hours (AUEC0-24), and the maximum effect ratio over baseline (ERmax).

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria
  • INCLUSION CRITERIA:

A subject will be considered eligible for this study only if all of the following criteria are met:

  1. Between the ages 18 70 years.
  2. Judged to be healthy based on medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory tests (liver function tests [LFTs] less than or equal to 2 times upper limit of normal [ULN], serum creatinine [sCr] less than or equal to ULN.
  3. Subject agrees to storage of specimens for future research.
  4. Negative serum or urine pregnancy test for females of child-bearing potential.
  5. For female subjects, willing to prevent pregnancy by (a) practicing abstinence or (b) using effective non-hormonal and/or barrier methods of birth control, during the study period.

EXCLUSION CRITERIA:

A subject will be ineligible for this study if 1, or more, of the following criteria are met:

  1. History of HIV exposure/infection, as determined by positive ELISA/ Western Blot.
  2. History or presence of any of the following:

    • gastrointestinal disease, that is uncontrolled or requires daily treatment with medication (pancreatitis, peptic ulcer disease, etc.)
    • hepatitis (as assessed by patient interview) or hepatic impairment
    • renal impairment (chronic or acute renal failure or insufficiency)
    • respiratory disease, that is uncontrolled or requires daily treatment with medication (asthma, chronic obstructive pulmonary disease, etc.)
    • cardiovascular disease (hypertension [systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg], heart failure,arrhythmia, etc.)
    • metabolic disorders (diabetes mellitus, etc.)
    • immunologic disorders
    • hormonal disorders
    • psychiatric illness, that would interfere with his or her ability to comply with study procedures or that requires daily treatment with medication
    • seizure disorder, with the exception of childhood febrile seizures
    • malignancy, or P-3 Pharmacoenhancers & Pradaxa, a P-gp Substrate 26
    • 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.
  3. History or presence of the following:

    • bleeding/hematologic disorders (hemophilia, etc.)
    • serious/major bleeding event (intracranial, gastrointestinal, as assessed by patient interview)

      c. current increased risk of bleeding (as indicated by aPTT > 1.5 times ULN], platelets, PLT, < 150,000/mm3, or Hgb < 11 g/dL)

      d. for female subjects, menorrhagia

  4. Planned invasive or surgical procedure within (prior to, or following) 28 days of study participation.
  5. Fasting total cholesterol > 270 mg/dL or fasting triglycerides > 270 mg/dL.
  6. Fasting glucose > 125 mg/dL.
  7. Concomitant routine therapy with any prescription, over-the-counter, herbal, or holistic medications, including hormonal contraceptives by any route, or any investigational drugs for 30 days prior to receipt of any study medications (Day 0).

    1. Concomitant therapy (chronic or intermittent) with any prescription, over-the-counter, herbal, or holistic medications will not be allowed during the study duration
    2. Intermittent use of acetaminophen and loperamide will be allowed to have been taken, according to each manufacturer s recommendations, within 30 days prior to study participation
    3. Intermittent use of acetaminophen, loperamide, and/or an antiemetic (as approved by the Principal Investigator) will be allowed to be taken according to each manufacturer s recommendations during the study. As P-gp substrates, loperamide and certain anti-emetics (i.e. ondansetron), should not be taken on the days of pharmacokinetic blood sampling
    4. A daily multivitamin with minerals will be allowed during the study
    5. Receipt of influenza vaccination will be allowed prior, during,

      and/or after the study

    6. Use of topical medications that are not significantly absorbed systemically will be allowed if approved by the Principal Investigator
  8. Inability to obtain venous access for sample collection.
  9. Inability to swallow whole capsules and/or tablets.
  10. Positive serum or urine pregnancy test or breastfeeding female.
  11. The presence of persistent diarrhea or malabsorption that could interferewith the subject s ability to absorb drugs.
  12. Drug or alcohol use that may impair safety or adherence.
  13. Use of nicotine-containing tobacco products, including cigarettes and chewing tobacco.
  14. History of intolerance or allergic reaction (rash; hives; swollen lips;difficulty breathing) to DE, RTV, or COBI.
  15. Organ transplant recipient.
  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: NCT01896622

Contacts
Contact: Parag Kumar, Pharm.D. (301) 496-0967 parag.kumar@nih.gov
Contact: Colleen M Hadigan, M.D. (301) 594-5754 hadiganc@mail.nih.gov

Locations
United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike Recruiting
Bethesda, Maryland, United States, 20892
Contact: For more information at the NIH Clinical Center contact Patient Recruitment and Public Liaison Office (PRPL)    800-411-1222 ext TTY8664111010    prpl@mail.cc.nih.gov   
Sponsors and Collaborators
Investigators
Principal Investigator: Colleen M Hadigan, M.D. National Institute of Allergy and Infectious Diseases (NIAID)
  More Information

Additional Information:
Publications:
Responsible Party: National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier: NCT01896622     History of Changes
Other Study ID Numbers: 130160, 13-CC-0160
Study First Received: July 6, 2013
Last Updated: August 1, 2014
Health Authority: United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):
Dabigatran Etexilate
Ritonavir
Cobicistat
P-Glycoprotein

Additional relevant MeSH terms:
Ritonavir
Dabigatran
HIV Protease Inhibitors
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Anti-HIV Agents
Anti-Retroviral Agents
Antiviral Agents
Anti-Infective Agents
Therapeutic Uses
Antithrombins
Serine Proteinase Inhibitors
Anticoagulants
Hematologic Agents

ClinicalTrials.gov processed this record on October 01, 2014