Why the study?
Does intravenous tenecteplase 0.25 mg/kg improve angiographic recanalization compared to intravenous alteplase 0.6 mg/kg in adult patients with acute ischemic stroke due to large vessel occlusion?
Does intravenous tenecteplase 0.25 mg/kg improve angiographic recanalization compared to intravenous alteplase 0.6 mg/kg in adult patients with acute ischemic stroke due to large vessel occlusion?
The ongoing T-FLAVOR trial is the first to directly compare the international standard dose of tenecteplase (0.25 mg/kg) with the Japan-specific low dose of alteplase (0.6 mg/kg) for acute ischemic stroke.
May support tenecteplase in hypertensive Asian stroke patients; leaves open confirmation in larger trials.
Intravenous thrombolysis for acute ischemic stroke is strongly recommended based on high-level evidence. However, the efficacy of the currently approved drug, alteplase, is not necessarily sufficient. Thrombolysis can trigger intracranial hemorrhage, that is a critical issue that cannot be overlooked, especially for Asians, who are generally hypertensive and prone to bleeding, making strict blood pressure control essential. Based on clinical trial results of a new thrombolytic agent, tenecteplase, several guidelines now recommend its use, and the off-label use has become common in many countries. As of 2024, regulatory approval has been granted in Western countries. Approval is also expected in major Asian countries between 2025 and 2026. In Japan, approval requires clinical data specific to Japanese patients, but no domestic pharmaceutical company currently handles the drug. We are conducting an investigator-initiated, multicenter, prospective, randomized, open-label, masked-endpoint, superiority trial, T-FLAVOR, comparing tenecteplase at 0.25 mg/kg (international standard dose) with alteplase at 0.6 mg/kg (a unique low dose approved in Japan). The target population consists of patients with ischemic stroke due to large vessel occlusion within 4.5 h of onset, who are also eligible for mechanical thrombectomy within 6 h. The primary efficacy outcome is successful early reperfusion assessed via catheter angiography after drug administration. Enrollment of the planned 220 participants was complete, and results are expected to be published in 2025. This is the only clinical trial using tenecteplase in Japan and the world's first to directly compare tenecteplase and low-dose alteplase (0.6 mg/kg).
No takes yet. Share an insight, caveat, or question.
Ḱazunori Toyoda (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: