# Advances in intravenous thrombolysis with tenecteplase in the ultra-time window

**Authors:** Zhen Wang, Hong-jian Guan, Lin-zhuo Qu, Qi Han, Yong Wang, Chun-hua Quan

PMC · DOI: 10.3389/fneur.2026.1724311 · 2026-02-18

## TL;DR

This paper reviews how tenecteplase improves stroke treatment beyond the traditional 4.5-hour window when used with imaging to identify suitable patients.

## Contribution

The paper systematically reviews recent clinical findings on tenecteplase's effectiveness in ultra-time window thrombolysis.

## Key findings

- Tenecteplase shows noninferiority to alteplase within 4.5 hours and better reperfusion in large vessel occlusions.
- Ultra-time window studies show tenecteplase improves outcomes for patients with ischemic penumbra between 4.5–24 hours.
- Some studies suggest reperfusion benefits without improved prognosis, highlighting the need for combined therapies and imaging.

## Abstract

Worldwide, stroke has become a significant public health concern, with ischemic strokes accounting for over 70% among all stroke types. Intravenous thrombolysis (IVT), as a traditional treatment method, is limited by a narrow 4.5-h time window, which restricts its application. The conception of a “tissue window” for imaging evaluation has prompted a change in treatment strategy in recent years, and the time window has been gradually expanded to 24 h. Tenecteplase (TNK), a third-generation thrombolytic medication with a long half-life, good fibrin specificity, and minimal risk of bleeding, has garnered significant research interest in ultra-time window thrombolysis. TNK is noninferior to alteplase (rt-PA) at 4.5 h and has a superior reperfusion rate in patients with large vessel occlusion in the anterior circulation, according to several phase III randomized controlled studies (e.g., AcT, TRACE-2, ORIGINAL). Ultra-time window studies (e.g., TRACE-3 and TIMELESS) have demonstrated that TNK has a positive safety profile and substantially enhances functional outcomes in patients who possess an ischemic penumbra detected by imaging screening for 4.5–24 h. Nevertheless, certain research (such as the CHABLIS-T II study) demonstrated that the application of ultra-time window intravenous thrombolysis improves reperfusion but doesn't improve the prognosis. Therefore, multicenter trials, coupled with neuroprotective medications or anti-inflammatory therapy, and dynamic imaging stratification are required to optimize intravenous thrombolysis strategies. This article serves as a reference for clinical practice and research direction by conducting a systematic review of the recent findings on ultra-time window thrombolysis in TNK.

## Linked entities

- **Diseases:** stroke (MONDO:0005098), ischemic stroke (MONDO:1060198)

## Full-text entities

- **Genes:** SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}
- **Diseases:** death (MESH:D003643), Basilar Artery Occlusion (MESH:D001157), Middle Vessel Occlusion Stroke (MESH:D020244), brain damage (MESH:D001925), thrombosis (MESH:D013927), reperfusion injury (MESH:D015427), Ischemic Cerebrovascular Events (MESH:D002561), artery (MESH:D012078), Ischemic Stroke (MESH:D002544), COVID-19 (MESH:D000086382), inflammatory drugs (MESH:D000081015), infarct (MESH:D007238), large artery blockage (MESH:D015508), NIHSS (MESH:C538175), inflammatory (MESH:D007249), Large Vessel Occlusion (MESH:C536223), ischemic (MESH:D002545), Non-Large Vessel Occlusion Stroke (MESH:D020521), intracranial hemorrhage (MESH:D020300), bleeding (MESH:D006470), hypoxia (MESH:D000860), non-small vessel occlusion (MESH:D059345), ischemia (MESH:D007511), neurological deficits (MESH:D009461), stenosis (MESH:D003251), AIS (MESH:D000083242)
- **Chemicals:** L-zQ (-), C-hQ (MESH:C004357)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** asparagine by glutamine at site 117, threonine by asparagine at site 103

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Source: https://tomesphere.com/paper/PMC12961998