Safety, Tolerability and Efficacy of Adjunctive TBO-309 in Reperfusion for Stroke With Tandem Occlusion

Recruiting Phase 2 Interventional Study
Ischemic Stroke Tandem Occlusion
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
78 (estimated)
Sponsor
ThromBio Pty. Ltd. · Industry
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About This Trial
Co-STAR is a multicenter, prospective, open-label, Bayesian Optimal Phase 2 (BOP2) trial that aims to assess the safety and efficacy of adjunctive intravenous TBO-309 in Acute Ischaemic Stroke (AIS) patients with tandem occlusion receiving intra-cranial endovascular thrombectomy (EVT) and acute extracranial carotid artery stenting. Co-STARS study will test the hypothesis that patients with tandem…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patient aged 18 years or more 2. Patient has an AIS due to tandem occlusion, including large vessel occlusion (LVO) within the intra-cranial anterior circulation and presumed atherosclerotic occlusion of the cervical internal carotid artery origin 3. CT perfusion indicates th…
Contacts

Ferdinand Miteff - Interventional Neurologist, RACP, CCINR

612 4921 3490

ferdi.miteff@health.nsw.gov.au

CONTACT

Candice Delcourt, MD, PhD and FRACP

61 2 8052 4601

cdelcourt@georgeinstitute.org.au

CONTACT