Mode
Text Size
Log in / Sign up
N/A N=110 Randomized Single-blind Treatment

Pharmacodynamic Effects of Prasugrel Compared With Ticagrelor in Patients With Coronary Artery Disease

Coronary Artery Disease

Enrolled (actual)
110
Serious AEs
0.0%
Results posted
Jun 2015
Primary outcome: Primary: Platelet Reactivity by Vasodilator-stimulated Phosphoprotein (VASP) — 32.1; 32.6 PRI%

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Prasugrel (Drug); Ticagrelor (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Florida
Primary completion
Jun 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Platelet Reactivity by Vasodilator-stimulated Phosphoprotein (VASP)
32.1; 32.6
SECONDARY
Platelet Reactivity Measured by Vasodilator-stimulated Phosphoprotein (VASP)
14.2; 26.4
SECONDARY
Platelet Reactivity Measured by Vasodilator-stimulated Phosphoprotein (VASP)
14.2; 26.4

Summary

Recently, two P2Y12 receptor inhibitors have been approved for clinical use: prasugrel and ticagrelor. Both prasugrel and ticagrelor have shown to be associated with more potent antiplatelet effects compared with clopidogrel and are associated with an improved net clinical benefit. However, to date there are limited head-to-head comparisons of these two new agents.

Eligibility Criteria

Inclusion Criteria

  • Patients with known coronary artery disease
  • On maintenance treatment with aspirin (81 mg per day) and clopidogrel (75 mg per day) for at least 1-month as per standard of care.
  • Age between 18 and 74 years old.

Exclusion Criteria

  • History of stroke, transient ischemic attack or intracranial bleeding.
  • Known allergies to aspirin, prasugrel, ticagrelor, or clopidogrel.
  • Weight 2.5 times the upper limit of normal.
  • Patients with sick sinus syndrome (SSS) or high degree AV block without pacemaker protection.
  • Drugs interfering with 2C19 metabolism (to avoid interaction with clopidogrel): , fluconazole (Diflucan), ketoconazole (Nizoral), voriconazole (VFEND), etravirine (Intelence), felbamate (Felbatol), fluoxetine (Prozac, Serafem, Symbyax), fluvoxamine (Luvox), and ticlopidine (Ticlid).
  • Drugs interfering CYP3A4 metabolism (to avoid interaction with Ticagrelor): Ketoconazole, itraconazole, voriconazole, clarithromycin, nefazodone, ritonavir, saquinavir, nelfinavir, indinavir, atazanavir, and telithromizycin.
  • Pregnant females*. *Women of childbearing age must use reliable birth control (i.e. oral contraceptives) while participating in the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01852175). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search