About this trial
This is a prospective, single-arm, open-label study to evaluate the efficacy of intra-arterial tenecteplase in improving microvascular reperfusion following successful large vessel recanalization. Acute ischemic stroke patients with large anterior circulation large vessel occlusion will receive a single weight-based dose of intra-arterial tenecteplase after achieving successful large vessel recanalization (defined as TICI ≥ 2b) via standard of care mechanical thrombectomy. Microvascular flow will be assessed by quantitative angiography before and after the intra-arterial drug administration in order to quantify the impact of targeted thrombolysis on microvascular reperfusion. Reperfusion will be secondarily assessed with 24-hour imaging, final infarct volume will be quantified 72 hours following treatment, and functional outcome will be assessed in the short-term by the NIHSS and in the long-term by the 90-day modified Rankin Scale.
Eligibility criteria
Qualifiers
Patient/legally authorized representative has signed the Informed Consent Form
At least 18 years of age
Ability to comply with the study protocol, in the investigator's judgment
Acute ischemic stroke attributed to anterior circulation large vessel occlusion (of the internal carotid artery or first segment of the middle cerebral artery based on CTA, MRA, or catheter angiogram) being treated with mechanical thrombectomy
Disqualifiers
Current participation in another investigational drug or device study
Known hypersensitivity or allergy to any ingredients of tenecteplase
Active internal bleeding
Known bleeding diathesis (Alzheimer's patients taking lecanemab)
Trial design
Treatments tested in this trial
- intra-arterial tenecteplase administration
Treatment groups
Sponsors and collaborators
University of Pennsylvania
Lead sponsor
Genentech, Inc.
Collaborator