While intravenous alteplase remains the standard thrombolytic for acute ischemic stroke, several trials now support alternative agents and delivery strategies. This review highlights key studies investigating tenecteplase (TNK), reteplase, and intra-arterial (IA) thrombolysis following thrombectomy.
Tenecteplase is a genetically engineered alteplase variant with higher fibrin specificity and longer half-life, allowing single bolus administration. It has shown promise in multiple RCTs:
The RAISE trial compared IV reteplase (18 mg + 18 mg) to standard alteplase within 4.5 hours of stroke onset:
Clinical Pearl: Reteplase is promising but not yet FDA-approved for stroke.
Several recent trials evaluated IA thrombolytics as adjunct therapy following successful mechanical thrombectomy, targeting residual microthrombi or no-reflow phenomena.
| Trial | Agent / Route | Time Window | mRS 0–1 | Safety |
|---|---|---|---|---|
| EXTEND-IA TNK | TNK IV (0.25 mg/kg) | <4.5 h | Improved vs tPA | No safety concerns |
| RAISE | Reteplase IV (18+18 mg) | <4.5 h | 79.5% vs 70.4% (tPA) | Similar ICH / death |
| CHOICE | IA tPA (0.225 mg/kg) | Post-MT | 59% vs 40% | No ↑ in sICH |
| ANGEL-TNK | IA TNK (0.125 mg/kg) | 4.5–24 h | 40.5% vs 26.4% | Safe |
| PEARL | IA tPA (0.225 mg/kg) | <24 h | 44.8% vs 30.2% | Safe |
With increasing evidence from multiple RCTs, both tenecteplase and reteplase show promise as alternatives to alteplase for acute ischemic stroke. Intra-arterial thrombolytics after thrombectomy also appear to enhance outcomes without added bleeding risk. As protocols evolve, these agents may become more integrated into personalized stroke reperfusion strategies.