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P2Y12 Receptor Inhibitor

Cangrelor for Heart Attack (CANTIC Trial)

Phase 4
Waitlist Available
Led By Dominick Angiolillo, MD, PhD
Research Sponsored by University of Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 minutes
Awards & highlights

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.

Eligible Conditions
  • Heart Attack
  • Percutaneous Coronary Intervention

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 minutes
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 minutes for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Platelet Reactivity Measured by VerifyNow PRU
Secondary outcome measures
Platelet Reactivity Measured by Vasodilator-stimulated Phosphoprotein (VASP)

Side effects data

From 2018 Phase 4 trial • 50 Patients • NCT03247738
12%
minor bleeding
100%
80%
60%
40%
20%
0%
Study treatment Arm
Cangrelor
Placebo

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: CangrelorExperimental Treatment1 Intervention
Cangrelor will be administered as 30 μg/kg bolus followed by 4 μg/kg/min infusion for 2 hours
Group II: PlaceboPlacebo Group1 Intervention
Normal saline bolus and infusion for 2 hours
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cangrelor
FDA approved

Find a Location

Who is running the clinical trial?

Chiesi Farmaceutici S.p.A.Industry Sponsor
200 Previous Clinical Trials
312,490 Total Patients Enrolled
University of FloridaLead Sponsor
1,354 Previous Clinical Trials
713,296 Total Patients Enrolled
Dominick Angiolillo, MD, PhDPrincipal InvestigatorUniversity of Florida College of Medicine-Jacksonville
8 Previous Clinical Trials
670 Total Patients Enrolled
~6 spots leftby Aug 2025