A Study to Investigate Biomarkers After Single Doses of Anticoagulants in Healthy Young Male and Healthy Elderly Participants (MK-0000-216 AM1)
A Randomized Clinical Trial to Validate Novel Biomarker Approaches After Single Doses of Anticoagulants in Healthy Young Male Subjects and in Healthy Elderly Subjects
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria for non-hemophilia participants:
Panel A
- Male or female between 65 to 85 years of age
Panel B
- Male between 18 to 45 years of age
Both Panels
- Weight of ≥50 kg and ≤110 kg
- In good health
- No clinically significant abnormality on electrocardiogram (ECG)
- Nonsmoker and/or has not used nicotine or nicotine-containing products for at least approximately 6 months
Exclusion criteria for non-hemophilia participants:
- History of stroke, chronic seizures, or major neurological disorder
- History of clinically significant endocrine, gastrointestinal (including peptic ulcer disease), cardiovascular, hematological, hepatic, immunological, renal, respiratory, or genitourinary abnormalities or diseases
- History of malignant neoplastic disease, with the exception of adequately treated non-melanomatous skin carcinoma or other malignancies that have been successfully treated ≥10 years prior to the study
- History of a thrombotic or platelet-related disorder including prior deep venous thrombosis or pulmonary embolus
- Use of warfarin, coumadin, heparin, aspirin, dabigatran etexilate, rivaroxaban or dipyridamole within 2 weeks
- History of poor wound healing
- Unable to refrain from or anticipates the use of any medication, including aspirin and aspirin-containing products, all non-steroidal anti-inflammatory drug (NSAID)-containing products (including pain, cold and allergy products, etc.) and including prescription and non-prescription drugs or herbal remedies (such as St. John's Wort [Hypericum perforatum]) beginning approximately 2 weeks (or 5 half-lives) prior to initiation of the treatment periods, throughout the study until the post-study visit
- Consumption of excessive amounts of alcohol, defined as greater than 3 glasses of alcoholic beverages (1 glass is approximately equivalent to: beer [284 mL/10 ounces], wine [125 mL/4 ounces], or distilled spirits [25 mL/1 ounce]) per day
- Consumption of excessive amounts, defined as greater than 6 servings (1 serving is approximately equivalent to 120 mg of caffeine) of coffee, tea, cola, or other caffeinated beverages per day
- Major surgery, donation or loss of 1 unit of blood (approximately 500 mL) or participation in another investigational study within 4 weeks
- History of significant multiple and/or severe allergies (including latex allergy), or an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs or food, including dabigatran etexilate and rivaroxaban
- Current regular user (including illicit drugs or has a history of drug [including alcohol] abuse within approximately 6 months
- History (including family history if hereditary) or symptoms of clinically relevant bleeding disorder
- Organic lesion at risk of bleeding (e.g., aneurysm, cavernous hemangioma, arterio-venous malformation)
- History of frequent epistaxis or has recurrent or active gingivitis or hemorrhoids
Inclusion criteria for hemophilia participants:
- Male with diagnosis of hemophilia B between 18 to 64 years of age
- Weight of ≥110 lbs and ≤300 lbs
- Has not received clotting factor in the 7 days prior to blood sampling
- No active bleeding event
- No procedure or surgery in the past 8 weeks
- Judged to be in good health based on medical history
- Has not smoked more than 2 cigarettes per day for at least approximately 1 week prior; has not smoked a pipe or cigar or chewed tobacco for at least 3 days prior
- Can refrain from the use of all NSAIDs (e.g., Advil, Aleve, aspirin), all NSAID-containing products (including pain, cold, and allergy products, etc.), herbal meds or drugs for 7 days prior to the date of study procedure
Exclusion criteria for hemophilia participants:
- Clinically significant endocrine, gastrointestinal (including peptic ulcer disease), cardiovascular, hematological (except factor IX deficiency), immunological, renal, respiratory, neurological or genitourinary abnormalities or diseases
- History of malignant neoplastic disease, with the exception of adequately treated non-melanomatous skin carcinoma or other malignancies that have been successfully treated ≥10 years prior to the study
- Consumption of excessive amounts of alcohol, defined as greater than 3 glasses of alcoholic beverages (1 glass is approximately equivalent to: beer [284 mL/10 ounces], wine [125 mL/4 ounces], or distilled spirits [25 mL/1 ounce]) within 24 hours prior to study procedures
- Major surgery, donation or loss of 1 unit of blood (approximately 500 mL) or participation in another investigational study within 7 days prior to the date of study procedures
- Current regular user (including illicit drugs or has a history of drug [including alcohol] abuse within approximately 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Dabigatran
Single 150-mg dose of dabigatran etexilate
|
dabigatran etexilate, orally, as 2 x 75-mg capsules (150 mg), single administration
|
|
Experimental: Rivaroxaban
Single 20-mg dose of rivaroxaban
|
rivaroxaban, orally, as 2 x 10-mg tablets (20 mg), single administration
|
|
No Intervention: No intervention
No study drug will be administered
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Endogenous thrombin potential by Thrombin Generation Assay (TGA)-2a assay
Time Frame: From up to 2 hours pre-dose to up to 24 hours post-dose
|
From up to 2 hours pre-dose to up to 24 hours post-dose
|
|
Level of fibrin degradation product (D-dimer)
Time Frame: From up to 2 hours pre-dose to up to 24 hours post-dose
|
From up to 2 hours pre-dose to up to 24 hours post-dose
|
|
Level of fibrinopeptide A (FPA)
Time Frame: From up to 2 hours pre-dose to up to 24 hours post-dose
|
From up to 2 hours pre-dose to up to 24 hours post-dose
|
|
Level of prothrombin split products (F1+2)
Time Frame: From up to 2 hours pre-dose to up to 24 hours post-dose
|
From up to 2 hours pre-dose to up to 24 hours post-dose
|
|
Level of thrombin-antithrombin complex (TAT)
Time Frame: From up to 2 hours pre-dose to up to 24 hours post-dose
|
From up to 2 hours pre-dose to up to 24 hours post-dose
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 0000-216
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.