Evaluate the Pharmacokinetics and Safety of MK-4448 in Participants With Nonvalvular Atrial Fibrillation or Atrial Flutter

NCT ID: NCT01229254

Last Updated: 2023-08-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 189 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-09-30
• Study Completion Date: 2011-04-30

Brief Summary

The primary purpose of this study is to optimize drug exposure in the target population.

Conditions

Atrial Fibrillation; Atrial Flutter

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Amiodarone

Participants on betrixaban 30 mg and concomitant baseline amiodarone

Group Type: EXPERIMENTAL

Amiodarone

Intervention Type: DRUG

Patients on Amiodarone

Betrixaban 30 mg

Intervention Type: DRUG

Betrixaban 30 mg once a day with food on Day 0 through Day 25 with concomitant amiodarone treatment.

Betrixaban 60 mg

Participants with lower weights

Group Type: EXPERIMENTAL

Betrixaban 60 mg

Intervention Type: DRUG

Betrixaban 60 mg once a day with food on Day 0 through Day 25

Betrixaban 90 mg

Participants with higher weights

Group Type: EXPERIMENTAL

Betrixaban 90 mg

Intervention Type: DRUG

Betrixaban 90 mg once a day with food on Day 0 through Day 25

Interventions

Amiodarone

Patients on Amiodarone

Intervention Type: DRUG

Betrixaban 60 mg

Betrixaban 60 mg once a day with food on Day 0 through Day 25

Intervention Type: DRUG

Betrixaban 90 mg

Betrixaban 90 mg once a day with food on Day 0 through Day 25

Intervention Type: DRUG

Betrixaban 30 mg

Betrixaban 30 mg once a day with food on Day 0 through Day 25 with concomitant amiodarone treatment.

Intervention Type: DRUG

Other Intervention Names

MK-4448; MK-4448; MK-4448

Eligibility Criteria

Inclusion Criteria

• In the opinion of the investigator, participant requires long term anticoagulation for stroke prevention in atrial flutter (AF).
• Men and women ≥18 years of age.
• Participant has current non-valvular atrial fibrillation (NVAF) or AF or electrocardiogram (ECG) or Holter documentation within past 12 months.
• Participant has an international normalized ratio (INR) ≤ 2.2 at allocation (Visit 2).
• A participant who is of reproductive potential agrees to remain abstinent or use (or have their partner use) 2 acceptable methods of birth control for the duration of the study. Acceptable methods of birth control are: intrauterine device (IUD), diaphragm with spermicide, condom, vasectomy, and hormonal contraception.
• Participant understands the study procedures and risks involved with the study, and voluntarily agree to participate by giving written informed consent.

Exclusion Criteria

General

• Participant is currently participating in another drug study or has received an investigational drug within 30 days prior to enrollment.
• Participant is a woman who is pregnant, lactating or of child-bearing potential who refuses to use a medically acceptable form of contraception throughout the study.
• Participant has a body weight less than 40 kg (88 lbs) or greater than 200 kg (440 lbs).
• Participant routinely consumes more than 2 alcoholic drinks per day (average >14 alcoholic drinks per week) or greater than 5 drinks within 2 hours on occasion.

Prohibited Medical Conditions

• Participant has any condition or situation which, in the opinion of the investigator, might pose a risk to the participant or interfere with participation in the study.
• Conditions associated with an increased risk of bleeding Active bleeding.
• Conditions other than AF that require chronic anticoagulation.
• Severe aortic and mitral valvular disease requiring surgical intervention.
• Previous known history of coagulopathy (e.g.: Factor V Leiden, Protein C Deficiency, Protein S Deficiency, Antiphospholipid Syndrome, etc.).
• Active infective endocarditis.
• Participant has history of familial long QT interval (the QT interval is the portion of an electrocardiogram (ECG) between the onset of the Q wave and the end of the T wave, representing the total time for ventricular depolarization and repolarization) syndrome or prolonged Bazett-corrected QT interval (QTcB) (males > 470 msec; females >480 msec) at baseline as measured on a 12-lead ECG.
• Participant has serious pulmonary, hepatic, metabolic, gastrointestinal, central nervous system (CNS) or psychiatric disease, end-stage disease states, or any other disease that could interfere with the conduct or validity of the study or compromise participant safety.
• Participant has a history of malignancy ≤ 5 years prior to signing informed consent, except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer (melanoma, leukemia, lymphoma and myeloproliferative disorders of any duration are excluded).
• Participant has a history of mental instability, drug/alcohol abuse within the past 5 years, or major psychiatric illness not adequately controlled and stable on pharmacotherapy.
• Participant has reversible causes of atrial fibrillation (i.e.: cardiac surgery, pulmonary embolism, untreated hyperthyroidism).
• Participant is to undergo pulmonary vein isolation or surgery for treatment of AF.
• Participant had a severe, disabling stroke within the previous 6 months, any stroke within the previous 14 days, thromboembolism within previous 30 days or a transient ischemic attack (TIA) within 3 days prior to Visit 1.
• Participant requires renal replacement therapies (hemo- or peritoneal dialysis).
• Participant has any of a list of defined laboratory abnormalities.

Prohibited Medications

• Anti-platelet agents other than aspirin within 10 days prior to Visit 1 (excluding maintenance dose clopidogrel, prasugrel or ticlopidine) or fibrinolytic agents within 30 days prior to Visit 1.
• Aspirin greater than 162 mg/day.
• Daily non-steroidal anti-inflammatory drug (NSAID) use.
• Dronedarone, verapamil or ketoconazole.
• Vitamin K antagonists (VKA) or other anticoagulants.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Portola Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

006-00

Identifier Type: -

Identifier Source: org_study_id