Key result
Tenecteplase provides a practical single-bolus alternative to alteplase for acute ischemic stroke.
Why the study?
Although tenecteplase has emerged as an alternative to alteplase for acute ischemic stroke, clinical adoption varies across regions due to regulatory approval, reimbursement, safety concerns, and limited real-world data from Asia. This review examines the evidence, workflow implications, and unresolved questions regarding tenecteplase, focusing on Asian stroke systems.
Does tenecteplase improve functional outcomes and recanalization compared to alteplase in patients with acute ischemic stroke?
Does tenecteplase improve functional outcomes and recanalization compared to alteplase in patients with acute ischemic stroke?
This review summarizes the clinical trial evidence supporting single-bolus tenecteplase (0.25 mg/kg) as an effective, workflow-friendly alternative to alteplase for acute ischemic stroke and details ongoing efforts, such as the T-FLAVOR trial, to overcome regulatory and dosing challenges in Japan and Asia.
May streamline workflows in eligible stroke patients; leaves open Asian dosing and real-world evidence needs pending T-FLAVOR.
Tenecteplase has emerged as a practical, evidence-supported thrombolytic alternative for acute ischemic stroke, challenging the long-standing predominance of alteplase. Greater fibrin specificity, resistance to plasminogen activator inhibitor-1, a longer half-life, and single-bolus administration provide a strong pharmacologic rationale for its use in time-sensitive stroke care. Accumulating evidence from randomized trials and meta-analyses suggests that tenecteplase 0.25 mg/kg is a reasonable alternative to alteplase for eligible patients treated within 4.5 hours, with particular practical advantages for those with large vessel occlusion who may require transfer for endovascular thrombectomy. Recent trials have broadened the discussion to include imaging-selected treatment beyond the conventional time window and adjunctive intra-arterial administration after thrombectomy. However, implementation varies across regions, and regulatory approval, reimbursement, safety concerns, and limited real-world data from Asia continue to shape clinical adoption. This review examines the pharmacologic rationale, clinical trial evidence, evolving guidelines, workflow implications, and unresolved questions surrounding tenecteplase for acute ischemic stroke, focusing on its potential role in Asian stroke systems.
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Kim et al. (2026) conducted a review in Acute ischemic stroke. Tenecteplase vs. Alteplase (0.9 mg/kg globally; 0.6 mg/kg in Japan) was evaluated. Tenecteplase 0.25 mg/kg is a practical, single-bolus alternative to alteplase for acute ischemic stroke within 4.5 hours, and the ongoing 220-patient T-FLAVOR trial in Japan compares it against 0.6 mg/kg alteplase.
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