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Phase 4 N=50 Randomized Quadruple-blind Treatment

Platelet Inhibition With Cangrelor and Crushed Ticagrelor in STEMI

ST Segment Elevation Myocardial Infarction · Percutaneous Coronary Intervention

Enrolled (actual)
50
Serious AEs
2.0%
Results posted
Feb 2020
Primary outcome: Primary: Platelet Reactivity Measured by VerifyNow PRU — 63; 214 P2Y12 reaction units (PRU) — p=<0.001

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Cangrelor (Drug); Placebo (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Florida
Primary completion
Dec 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Platelet Reactivity Measured by VerifyNow PRU
63; 214 <0.001 sig
SECONDARY
Platelet Reactivity Measured by Vasodilator-stimulated Phosphoprotein (VASP)
29; 72

Summary

In STEMI patients undergoing PPCI there is a delayed onset of action of oral P2Y12 receptor inhibitors, including prasugrel and ticagrelor. Crushing prasugrel and ticagrelor improves their PK and PD profiles as it favors drug absorption and onset of antiplatelet effects and because of this, it is commonly used in STEMI patients undergoing PPCI. However, despite the use of crushed tablets, up to one-third of patients may still have high on-treatment platelet reactivity (HPR) within the first 2 hours after loading dose (LD) administration of these oral agents. Cangrelor is a potent intravenous P2Y12 receptor inhibitor with rapid onset and offset of action associated with a greater reduction in ischemic events compared with clopidogrel in P2Y12 receptor naïve patients undergoing PCI. To date most studies have explored cangrelor in the setting of PCI subjects treated with clopidogrel. The PD effects of cangrelor in STEMI patients undergoing PPCI treated with a newer generation P2Y12 receptor inhibitor and how this compares with a crushed formulation of the oral drug is unexplored. The aim of this prospective randomized study is to investigate the PD effects of cangrelor in STEMI patients undergoing PPCI treated with crushed ticagrelor.

Eligibility Criteria

Inclusion criteria

  • Patients with STEMI undergoing primary PPCI
  • Age > 18 years old

Exclusion criteria

  • Inability to provide written informed consent
  • Known history of prior intracranial bleeding
  • On treatment with a P2Y12 receptor antagonist (ticlopidine, clopidogrel, prasugrel, ticagrelor) in the prior 10 days
  • Known allergies to aspirin, ticagrelor or cangrelor
  • On treatment with oral anticoagulant
  • Treatment with glycoprotein IIb/IIIa inhibitors
  • Fibrinolytics within 24 hours
  • Active bleeding
  • High risk of bleeding
  • Known platelet count <80x106/mL
  • Known hemoglobin <10 g/dL
  • Intubated patients (prior to randomization)
  • Known creatinine clearance <30 mL/minute or on hemodialysis.
  • Known severe hepatic dysfunction
  • Patients with sick sinus syndrome (SSS) or high degree AV block without pacemaker protection
  • Current treatment with drugs interfering with CYP3A4 metabolism (to avoid interaction with ticagrelor): Ketoconazole, itraconazole, voriconazole, clarithromycin, nefazodone, ritonavir, saquinavir, nelfinavir, indinavir, atazanavir, and telithromizycin.
  • Pregnant or lactating females.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03247738). 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.

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