4.2 Article

Clopidogrel with aspirin in High-risk patients with Acute Non-disabling Cerebrovascular Events II (CHANCE-2): rationale and design of a multicentre randomised trial

Journal

STROKE AND VASCULAR NEUROLOGY
Volume 6, Issue 2, Pages 280-285

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/svn-2020-000791

Keywords

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Funding

  1. National Science and Technology Major Project [2017ZX09304018]
  2. Beijing Municipal Science and Technology Commission [D171100003017002]
  3. Ministry of Science and Technology of the People's Republic of China (MOST)
  4. Beijing Municipal Science and Technology Commission
  5. Chinese Stroke Association (CSA) fund CHANCE-2

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The CHANCE-2 trial aims to compare the efficacy and safety of different dual antiplatelet strategies (ticagrelor-aspirin and clopidogrel-aspirin) for CYP2C19 LOF allele carriers with minor stroke or TIA.
Background In patients with a minor ischaemic stroke or transient ischaemic attack (TIA), separate trials have shown that dual antiplatelet therapy with clopidogrel plus aspirin (clopidogrel-aspirin) or ticagrelor plus aspirin (ticagrelor-aspirin) are more effective than aspirin alone in stroke secondary prevention. However, these two sets of combination have not been directly compared. Since clopidogrel was less effective in stroke patients who were CYP2C19 loss-of-function (LOF) allele carriers, whether ticagrelor-aspirin is clinically superior to clopidogrel-aspirin in this subgroup of patients with stroke is unclear. Aim To describe the rationale and design considerations of the Clopidogrel in High-risk patients with Acute Non-disabling Cerebrovascular Events (CHANCE-2) trial. Design CHANCE-2 is a randomised, double-blind, double-dummy, placebo-controlled, multicentre trial that compares two dual antiplatelet strategies for minor stroke or TIA patients who are CYP2C19 LOF allele carriers: ticagrelor (180 mg loading dose on day 1 followed by 90 mg twice daily on days 2-90) or clopidogrel (300 mg loading dose on day 1 followed by 75 mg daily on days 2-90), plus open-label aspirin with a dose of 75-300 mg on day 1 followed by 75 mg daily on day 2-21. All will be followed for 1 year. Study outcomes The primary efficacy outcome is any stroke (ischaemic or haemorrhagic) within 3 months and the primary safety outcome is any severe or moderate bleeding event within 3 months. Discussion The CHANCE-2 trial will evaluate whether ticagrelor-aspirin is superior to clopidogrel-aspirin for minor stroke or TIA patients who are CYP2C19 LOF allele carriers.

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