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Completed

NCT Number: NCT00684203

Trial to Assess the Safety and Effects of Vorapaxar in Japanese Subjects With Acute Coronary Syndrome (P04772; MK-5348-016)

The study is designed to assess safety and effects of vorapaxar, when added to standard of care (aspirin and clopidigrel), in Japanese subjects with acute coronary syndrome. The study may also provide information about the effect of vorapaxar on preventing heart attack and stroke in this subject population.

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Key information

Conditions

Atherosclerosis Arterial Occlusive Diseases Arteriosclerosis Cardiovascular Diseases Heart Diseases Infarction Ischemia Myocardial Infarction Myocardial Ischemia Necrosis Pathologic Processes Pathological Conditions, Signs and Symptoms Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

About this study

The study drug (loading dose) is administered at least 1 hour before catheterization for diagnostic imaging or percutaneous coronary interventions (PCI). The incidence of bleeding is thought to be an important index to assess the safety of this drug, therefore thrombolysis in myocardial infarction (TIMI) is evaluated.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women aged 18 years or more with history of cardiac ischemia related chest discomfort of > 10 minutes duration < 24 hours prior to randomization, and having at least 1 of the following A or B. Participants who are planned to undergo PCI will be the target participants.
  • A: Positive biomarkers [Elevated troponin I or creatinine kinase MB isozyme greater than the site's upper limit of normal (ULN)] at or before registration
  • B: Electrocardiogram (ECG) changes: ST segment depression >= 0.1 mV (>=1 mm), or transient (<30 minutes) ST segment elevation >= 0.1 mV (>=1 mm) in at least 2 contiguous leads
  • Willing to give appropriate informed consent and complete all study-related procedures, and able to adhere to dosing and all visit schedules.
  • Women of child-bearing potential (all postmenarchal women who are <1 years menopausal or who have not had surgical sterilization or a hysterectomy are considered to be women of child-bearing potential) must agree to use a medically accepted method of contraception while receiving protocol-specified medication, and for 60 days after stopping the medication.

Exclusion criteria

  • Pregnant and nursing mothers (premenopausal women should have a negative pregnancy test result confirmed before enrollment)
  • Any serious illness or any condition that the investigator feels would pose a significant hazard to the participant if investigational therapy were initiated
  • known hypersensitivity to any component of the current investigational product;
  • Participation in a study of experimental therapy or use of any investigational drug within 30 days before enrollment
  • Member of the staff personnel directly involved with this study;
  • Family member of the investigational study staff;
  • History of a bleeding diathesis, or evidence of active abnormal bleeding within 30 days before enrollment
  • History of a hemorrhagic stroke at any time
  • Severe hypertension (systolic blood pressure >200 mm Hg or diastolic blood pressure >110 mm Hg) while receiving therapy;
  • Major surgery within 2 weeks prior to enrollment
  • Known platelet count <100,000/mm^3
  • Uncontrolled cardiac arrhythmia;
  • Known impairment of renal function (serum creatinine >2.0 mg/dL [>176.8 umol/L]), dysproteinemia, nephrotic syndrome, or other renal disease;
  • Active or chronic hepatobiliary or hepatic disease, or aspartate aminotransferase (AST) or alanine aminotransferase (ALT) activity more than two times greater than the upper limit of the laboratory reference range
  • Anticipated staged PCI
  • Concurrent or anticipated treatment with warfarin, factor Xa inhibitor, direct thrombin inhibitor, or antiplatelet agents except aspirin and ticlopidine after enrollment
  • Anticipated intracoronary brachytherapy

Treatment and study plan

Vorapaxar

Drug

Oral tablets; single 20-mg or 40-mg loading dose on first day followed by daily 1-mg or 2.5-mg maintenance dose for 59 days

Placebo

Drug

Oral tablets; matching placebo for SCH 530348 loading and maintenance doses for 59 days

Aspirin

Drug

Loading dose of 75-325 mg on Day 1, then 75-100 mg once daily for 60 days.

Other names: ASA, acetylsalicylic acid

clopidogrel

Drug

100 mg two or three times daily for 60 days.

Primary outcomes

  1. Number of Participants Experiencing Adverse Events (AEs) Who Underwent Percutaneous Coronary Interventions (PCI)

    Time frame: Up to Day 60

    An AE is any unfavorable and unintended change in the structure, function or chemistry of the body temporally associated with study drug administration, whether or not considered related to the study drug.

Secondary outcomes

  1. Number of Participants Experiencing Non-Major Adverse Cardiac Events (MACE) Who Underwent PCI

    Time frame: Up to Day 121

    An AE is any unfavorable and unintended change in the structure, function or chemistry of the body temporally associated with study drug administration, whether or not considered related to the study drug. MACE events were defined as nonfatal myocardial infarction (MI), nonfatal stroke, hospitalization due to recurrent ischemia, or urgent coronary revascularization performed ≥ 30 days after administration of the loading dose (Day 1). All MACE events were excluded from this analysis. Analysis of data was by loading/maintenance dose group.

  2. Number of Participants With Major, Minor, and Non-Thrombolysis in Myocardial Infarction Cooperative Group (TIMI) Bleeding Events Among Participants Who Underwent PCI

    Time frame: Up to Day 60

    Major TIMI bleeding was defined as any intracranial bleeding (excluding microhemorrhages <10 mm evident only on gradient-echo magnetic resonance imaging [MRI]), clinically overt signs of hemorrhage associated with a drop in hemoglobin of ≥5 g/dL, or fatal bleeding (bleeding that directly results in death within 7 days). Minor TIMI bleeding was defined as any clinically overt bleeding resulting in hemoglobin drop of 3 to <5 g/dL. Non-TIMI bleeding included all bleeding events not covered under Major TIMI bleeding or Minor TIMI bleeding. Analysis of data was by maintenance dose group.

  3. Number of Participants Who Underwent PCI With Inhibition of Platelet Aggregation By Study Visit

    Time frame: Baseline, Day 30, Day 60, Day 74, Day 90, Day 121

    Blood samples were collected from participants at Baseline and Days 30, 60, 74, 90, and 121 to determine the extent of inhibition of platelet aggregation induced by thrombin-receptor agonist peptide (TRAP). Analysis of data was by maintenance dose group.

  4. Median High-Sensitivity C-Reactive Protein (Hs-CRP) Levels Among Participants Who Underwent PCI By Study Visit

    Time frame: Baseline, Day 30, Day 60

    Participant blood samples were collected at Baseline and on Days 30 and 60 to evaluate the median level of hs-CRP. hs-CRP is a protein marker in the blood associated with inflammation with higher values indicating a greater degree of inflammation. Analysis of data was by maintenance dose group.

  5. Mean CD40 Ligand Levels Among Participants Who Underwent PCI

    Time frame: Baseline, Day 30, Day 60

    Participant blood samples were collected at Baseline and Days 30 and 60 to evaluate the mean level of CD40 ligand present. CD40 ligand is a protein primarily found on activated T-cells, with higher levels indicating better immunological health. Analysis of data was by maintenance dose group.

  6. Mean Membrane-Bound P-Selectin Levels Among Participants Who Underwent PCI

    Time frame: Baseline, Day 30, Day 60

    Participant blood samples were collected at Baseline and Days 30 and 60 to evaluate the mean level of membrane-bound P-selectin. Membrane-bound P-selectin was measured using flow cytometry and a monoclonal antibody to P-selectin. Intensity levels are reported in arbitrary units 0 (dark) to 1023 (bright). Higher values correspond to greater membrane-bound P-Selectin levels. Analysis of data was by maintenance dose group.

  7. Number of Participants Who Underwent PCI With Clinically Important Bleeding Events During Treatment and After Hospital Discharge

    Time frame: Up to Day 121

    Clinically important bleeding events were defined as intracranial hemorrhage, bleeding requiring hospitalization, or TIMI major bleeding. Analysis of data was by loading/maintenance dose group.

  8. Number of Participants With Major, Minor, and Non-TIMI Bleeding Events Among Participants Who Did Not Undergo PCI

    Time frame: Up to Day 60

    Major TIMI bleeding was defined as any intracranial bleeding (excluding microhemorrhages <10 mm evident only on gradient-echo MRI), clinically overt signs of hemorrhage associated with a drop in hemoglobin of ≥5 g/dL, or fatal bleeding (bleeding that directly results in death within 7 days). Minor TIMI bleeding was defined as any clinically overt bleeding resulting in hemoglobin drop of 3 to <5 g/dL. Non-TIMI bleeding included all bleeding events not covered under Major TIMI bleeding or Minor TIMI bleeding. Analysis of data was by loading dose group.

  9. Number of Participants Experiencing Non-MACE AEs Among Participants Who Did Not Undergo PCI

    Time frame: Up to Day 121

    An AE is any unfavorable and unintended change in the structure, function or chemistry of the body temporally associated with study drug administration, whether or not considered related to the study drug. MACE events were defined as nonfatal MI, nonfatal stroke, hospitalization due to recurrent ischemia, or urgent coronary revascularization performed ≥ 30 days after administration of the loading dose (Day 1). All MACE events were excluded from this analysis. Analysis of data was by loading dose group.

  10. Number of Participants Who Did Not Undergo PCI But Had Coronary Artery Bypass Graft (CABG) Who Experienced Bleeding Events

    Time frame: Up to 10 Hours Post-CABG

    Bleeding events were evaluated up to 10 hours post-CABG among participants who did not undergo PCI.

  11. Number of Participants Who Did Not Undergo PCI But Had Bleeding Events That Required Transfusion

    Time frame: Up to Day 60

    Bleeding events were evaluated among participants that did not undergo PCI to determine the number of participants that required blood transfusion. Analysis of data was by loading dose group.

  12. Number of Participants Who Did Not Undergo PCI But Had Bleeding Events That Required Subsequent Hospitalization

    Time frame: Up to Day 30

    Bleeding events were evaluated among participants that did not undergo PCI to determine the number of participants who required a subsequent hospitalization. Analysis of data was by loading dose group.

  13. Median Hs-CRP Levels Among Participants Who Did Not Undergo PCI

    Time frame: Baseline Up To Day 60

    Participant blood samples were collected at baseline and at the time of hospital discharge to determine the median serum level of hs-CRP. Analysis of data was by loading dose group.

  14. Mean CD40 Ligand Levels Among Participants Who Did Not Undergo PCI

    Time frame: Baseline Up To Day 60

    Participant blood samples were collected at baseline and at the time of hospital discharge to determine the mean serum level of CD40 ligand. Analysis of data was by loading dose group.

  15. Number of Participants Who Did Not Undergo PCI That Had Clinically Important Bleeding Events

    Time frame: Baseline Up To Day 60

    Clinically important bleeding events were defined as intracranial hemorrhage, bleeding requiring blood transfusion, bleeding requiring hospitalization, and TIMI major bleeding. Analysis of data was by loading dose group.

Sponsors and collaborators

Lead sponsor

Merck Sharp & Dohme LLC

Industry

Registry information

Official study title

Phase II Study of SCH 530348 in Subjects With Acute Coronary Syndrome

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
May 26, 2008
Registry last updated
May 5, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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