Tenecteplase
Tenecteplase has been studied in 3 papers since 2022: 1 trial and 2 observational studies in people. The newest paper, Sep 2, 2025: “Brain Frailty and Functional Outcomes After Thrombolysis for Acute Ischemic Stroke”.
“Type of thrombolytic agent (TNK versus alteplase) did not modify the association between age and primary clinical outcome (Pinteraction=0.22).”
None of its findings points the other way.
- 2 independent labs in 1 country
- 4 trials, none about aging
- 1 of 3 findings with company ties
- Human trial1
- Humans2
Studies in people
1 study gave tenecteplase to people and measured what changed.
up: Improves functional outcomemedian 3 vs 4, acOR 2.70, 95% CI 1.23-5.94
down: Decreases mortalityacOR 0.34, 95% CI 0.13-0.91
Review of trials137 people pooled>80 years90 days
Older adults; The oldest old; Patient cohorts
Neurology, Jan 11, 2022
What did studies of Tenecteplase find?
3Studies of Tenecteplase measured 3 outcomes; the most studied are age-associated primary clinical outcome (1 study), mortality (1) and functional outcome (1).
Age-associated primary clinical outcome
no changein humans1
1 study
Age-associated primary clinical outcome
no changein humans1
Tenecteplase has no effect on age-associated primary clinical outcome in humans (Pinteraction=0.22).
“Type of thrombolytic agent (TNK versus alteplase) did not modify the association between age and primary clinical outcome (Pinteraction=0.22).”
Human trialacute ischemic stroke across age groupsn = 1,577
Stroke
Mortality
downin humans1
1 study
Mortality
downin humans1
Tenecteplase decreases mortality in humans (acOR 0.34, 95% CI 0.13-0.91).
“reduced mortality (acOR 0.34, 95% CI 0.13-0.91) vs 0.40 mg/kg.”
Human trialvs 0.40 mg/kg0.25 mg/kg90 daysn = 137
Neurology
Functional outcome
upin humans1
1 study
Functional outcome
upin humans1
Tenecteplase improves functional outcome in humans (median 3 vs 4, acOR 2.70, 95% CI 1.23-5.94).
“TNK 0.25 mg/kg was associated with improved 90-day mRS (median 3 vs 4, adjusted common odds ratio (acOR) 2.70, 95% CI 1.23-5.94) and reduced mortality (acOR 0.34, 95% CI 0.13-0.91) vs 0.40 mg/kg.”
Human trialvs 0.40 mg/kg0.25 mg/kg90 daysn = 137
Neurology
Trial sponsors
1 trialPhase 31,600 people
2 trialsPhase 2502 people