A Study on BMS-986177 for the Prevention of a Stroke in Patients Receiving Aspirin and Clopidogrel (AXIOMATIC-SSP)
Acute Ischemic Stroke, Transient Ischemic Attack (TIA)
About this trial
This is an interventional prevention trial for Acute Ischemic Stroke
Eligibility Criteria
Inclusion Criteria:
- Male and Female ≥40 years of age
- Acute Ischemic Stroke or Transient Ischemic Attack
- Intracranial or Extracranial Atherosclerotic Plaque proximal to the affected brain area
Exclusion Criteria:
- Predicted inability to swallow study medication
- Any condition that, in the opinion of the Investigator, contraindicates anticoagulant therapy or would have an unacceptable risk of bleeding
- Use of thrombolytic therapy or mechanical thrombectomy for treatment of index stroke
Other protocol defined inclusion/exclusion criteria could apply
Sites / Locations
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- Kaiser Permanente Los Angeles Medical Center
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- University of Illinois Hospital & Health Sciences System
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- Advanced Neurology Specialists PLLC
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- Duke University Medical Center
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- Temple University Hospital
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- Neurology Consultants of Dallas, PA
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Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Placebo Comparator
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
BMS-986177 Placebo
Dose 1: BMS-986177 + Aspirin + Clopidogrel
Dose 2: BMS-986177 + Aspirin + Clopidogrel
Dose 3: BMS-986177 + Aspirin + Clopidogrel
Dose 4: BMS-986177 + Aspirin + Clopidogrel
Dose 5: BMS-986177 + Aspirin + Clopidogrel
Dose 6: BMS-986177 + Aspirin + Clopidogrel
Dose 7: BMS-986177 + Aspirin + Clopidogrel
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days
Specified Dose on Specified Days