Skip to main content

Research Repository

Advanced Search

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

Wang, Yongjun; Claiborne Johnston, S.; Bath, Philip M.; Meng, Xia; Jing, Jing; Xie, Xuewei; Wang, Anxin; Pan, Yuesong; Xu, Anding; Dong, Qiang; Wang, Yilong; Zhao, Xingquan; Li, Zixiao; Li, Hao

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


Authors

Yongjun Wang

S. Claiborne Johnston

Xia Meng

Jing Jing

Xuewei Xie

Anxin Wang

Yuesong Pan

Anding Xu

Qiang Dong

Yilong Wang

Xingquan Zhao

Zixiao Li

Hao Li



Abstract

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.

Citation

Wang, Y., Claiborne Johnston, S., Bath, P. M., Meng, X., Jing, J., Xie, X., Wang, A., Pan, Y., Xu, A., Dong, Q., Wang, Y., Zhao, X., Li, Z., & Li, H. (2021). Clopidogrel with aspirin in High-risk patients with Acute Non-disabling Cerebrovascular Events II (CHANCE-2): rationale and design of a multicenter randomised trial. Stroke and Vascular Neurology, 6(2), Article e000791. https://doi.org/10.1136/svn-2020-000791

Journal Article Type Article
Acceptance Date Apr 9, 2021
Online Publication Date May 5, 2021
Publication Date 2021-06
Deposit Date Apr 16, 2021
Publicly Available Date May 5, 2021
Journal Stroke and Vascular Neurology
Electronic ISSN 2059-8696
Publisher BMJ Publishing Group
Peer Reviewed Peer Reviewed
Volume 6
Issue 2
Article Number e000791
DOI https://doi.org/10.1136/svn-2020-000791
Public URL https://nottingham-repository.worktribe.com/output/5469316
Publisher URL https://svn.bmj.com/content/early/2021/05/05/svn-2020-000791
Additional Information Authors for the CHANCE-2 Investigators.

Files





You might also like



Downloadable Citations