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Clinical Trials/NCT05779059
NCT05779059
Not yet recruiting
Phase 3

Prasugrel Or Ticagrelor De-escalation in Non-ST-elevation Acute Coronary Syndrome

Collegium Medicum w Bydgoszczy1 site in 1 country50 target enrollmentStarted: April 1, 2023Last updated:

Overview

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Collegium Medicum w Bydgoszczy
Enrollment
50
Locations
1
Primary Endpoint
Platelet Reactivity Assessed with Multiple Electrode Aggregometry

Overview

Brief Summary

The PROTEUS study is a randomized, cross-over, open-label, pharmacodynamic trial designed to compare the antiplatelet effect of reduced maintenance doses of prasugrel and ticagrelor in stable patients who recently had non-ST-elevation acute coronary syndrome (non-ST-elevation myocardial infarction or unstable angina).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • provision of informed consent prior to any study specific procedures
  • diagnosis of non-ST-segment elevation acute coronary syndrome (non-ST-segment elevation myocardial treatment or unstable angina)
  • male or non-pregnant female, aged 18-75 years old

Exclusion Criteria

  • known hypersensitivity to ticagrelor or prasugrel
  • presence of contraindications for ticagrelor or prasugrel
  • current treatment with oral anticoagulant or chronic therapy with low-molecular-weight heparin
  • history of ischemic stroke or transient ischemic attack
  • history of intracranial hemorrhage
  • recent gastrointestinal bleeding (within 30 days)
  • history of moderate or severe hepatic impairment
  • history of major surgery or severe trauma (within 3 months)
  • patient required dialysis
  • concomitant therapy with strong CYP3A inhibitors (ketoconazole, itraconazole, voriconazole, telithromycin, clarithromycin, nefazadone, ritonavir, saquinavir, nelfinavir, indinavir, atazanavir) or strong CYP3A inducers (rifampicin, phenytoin, carbamazepine, dexamethasone, phenobarbital) within 14 days and during study treatment

Arms & Interventions

Initial ticagrelor

Experimental

All patients will receive standard 180 mg loading dose of ticagrelor, followed by a standard maintenance dose of 90 mg bid for 30 days, after which de-escalation to 60 mg bid will take place and this dosing will be maintained for 15 days. At day 45 all patients will be loaded with standard 60 mg dose of prasugrel followed by reduced maintenance dose of 5 mg qd for 15 days. At day 60 all patients will be switched back to guideline recommended antiplatelet therapy.

Intervention: De-escalation to ticagrelor 60 mg at day 30 (Drug)

Initial ticagrelor

Experimental

All patients will receive standard 180 mg loading dose of ticagrelor, followed by a standard maintenance dose of 90 mg bid for 30 days, after which de-escalation to 60 mg bid will take place and this dosing will be maintained for 15 days. At day 45 all patients will be loaded with standard 60 mg dose of prasugrel followed by reduced maintenance dose of 5 mg qd for 15 days. At day 60 all patients will be switched back to guideline recommended antiplatelet therapy.

Intervention: Switch to prasugrel 5 mg at day 45 (Drug)

Initial prasugrel

Experimental

All patients will receive standard 60 mg loading dose of prasugrel, followed by a standard maintenance dose 10 mg qd for 30 days, after which de-escalation to 5 mg qd will take place and this dosing will be maintained for 15 days. At day 45 patients will be loaded with standard 180 mg dose of ticagrelor followed by reduced maintenance dose of 60 mg bid for 15 days. At day 60 all patients will be switched back to guideline recommended antiplatelet therapy.

Intervention: De-escalation to prasugrel 5 mg at day 30 (Drug)

Initial prasugrel

Experimental

All patients will receive standard 60 mg loading dose of prasugrel, followed by a standard maintenance dose 10 mg qd for 30 days, after which de-escalation to 5 mg qd will take place and this dosing will be maintained for 15 days. At day 45 patients will be loaded with standard 180 mg dose of ticagrelor followed by reduced maintenance dose of 60 mg bid for 15 days. At day 60 all patients will be switched back to guideline recommended antiplatelet therapy.

Intervention: Switch to ticagrelor 60 mg at day 45 (Drug)

Outcomes

Primary Outcomes

Platelet Reactivity Assessed with Multiple Electrode Aggregometry

Time Frame: day 15 of using reduced maintenance dose of prasugrel or ticagrelor

Platelet Reactivity Assessed with Multiple Electrode Aggregometry will be evaluated after 15 days of using reduced maintenance dose of prasugrel or ticagrelor.

Secondary Outcomes

  • High Platelet Reactivity according to Multiple Electrode Aggregometry(day 15 of using reduced maintenance dose of prasugrel or ticagrelor)
  • High Platelet Reactivity according to the VerifyNow assay(day 15 of using reduced maintenance dose of prasugrel or ticagrelor)
  • Platelet Reactivity Assessed with the VerifyNow assay(day 15 of using reduced maintenance dose of prasugrel or ticagrelor)

Investigators

Sponsor
Collegium Medicum w Bydgoszczy
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Piotr Adamski

MD, PhD, Associate Professor

Collegium Medicum w Bydgoszczy

Study Sites (1)

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