The multiarm optimization of stroke thrombolysis phase 3 acute stroke randomized clinical trial: Rationale and methods
- PMID: 33297893
- PMCID: PMC8926066
- DOI: 10.1177/1747493020978345
The multiarm optimization of stroke thrombolysis phase 3 acute stroke randomized clinical trial: Rationale and methods
Abstract
Background: Intravenous recombinant tissue plasminogen activator is the only proven effective medication for the treatment of acute ischemic stroke. Two approaches that may augment recombinant tissue plasminogen activator thrombolysis and prevent arterial reocclusion are direct thrombin inhibition with argatroban and inhibition of the glycoprotein 2b/3a receptor with eptifibatide.
Aim: The multi-arm optimization of stroke thrombolysis trial aims to determine the safety and efficacy of intravenous therapy with argatroban or eptifibatide as compared with placebo in acute ischemic stroke patients treated with intravenous recombinant tissue plasminogen activator within 3 h of symptom onset.
Sample size estimate: A maximum of 1200 randomized subjects to test the superiority of argatroban or eptifibatide to placebo in improving 90-day modified Rankin scores.
Methods and design: Multiarm optimization of stroke thrombolysis is a multicenter, multiarm, adaptive, single blind, randomized controlled phase 3 clinical trial conducted within the National Institutes of Health StrokeNet clinical trial network. Patients treated with 0.9 mg/kg intravenous recombinant tissue plasminogen activator within 3 h of stroke symptom onset are randomized to receive intravenous argatroban (100 µg/kg bolus followed by 3 µg/kg/min for 12 h), intravenous eptifibatide (135 µg/kg bolus followed by 0.75 µg/kg/min infusion for 2 h) or IV placebo. Patients may receive endovascular thrombectomy per usual care.
Study outcomes: The primary efficacy outcome is improved modified Rankin score assessed at 90 days post-randomization.
Discussion: Multiarm optimization of stroke thrombolysis is an innovative and collaborative project that is the culmination of many years of dedicated efforts to improve outcomes for stroke patients.
Trial registration: ClinicalTrials.gov NCT03735979.
Keywords: Acute ischemic stroke; alteplase recombinant tissue plasminogen activator; argatroban; clinical trial; eptifibatide; recanalization; recombinant tissue plasminogen activator.
Conflict of interest statement
Declaration of conflicting interests
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Colin P Derdeyn: Consultant – Penumbra (DSMB, MIND trial); Nono (DSMB, ESCAPE NA1 trial); Genae (DSMB Tigertriever trial); Equity – Pulse Therapeutics (Scientific Advisory Board, Stock Options). Joseph Broderick: Department of Neurology and Rehabilitation Medicine receives monies from Genentech Inc. for his role on Executive Committee of TIMELESS Trial. Opeolu Adeoye: Founder and Equity Holder, Sense Diagnostics, Inc.
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References
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- Rha JH and Saver JL. The impact of recanalization on ischemic stroke outcome: a meta-analysis. Stroke 2007; 38: 967–973. - PubMed
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