RecruitingPhase 2NCT07283159

Tenecteplase Plus Urinary Kallidinogenase for Acute Ischemic Stroke (TUKIS)

Tenecteplase Plus Urinary Kallidinogenase for Acute Ischemic Stroke (TUKIS): a Prospective, Randomized, Double Blinded and Multi-center Study

Sponsor

General Hospital of Shenyang Military Region

Enrollment

200 participants

Start Date

Jan 20, 2026

Study Type

INTERVENTIONAL

Conditions

Ischemic Stroke

Summary

Human urinary kallidinogenase (HUK) is a tissue kallikrein extracted from human urine. Under certain conditions, tissue kallikrein can convert kininogen into kallidin and kinins, thereby promoting vascular endothelial function, and exerting anti-inflammatory and antioxidant effects. Preclinical and clinical studies have demonstrated that HUK can salvage the ischemic penumbra and significantly promote the establishment of collateral circulation. Existing research suggests that the combination of HUK with intravenous alteplase significantly improves neurological function in patients with acute ischemic stroke (AIS) without increasing the risk of hemorrhage. However, whether its combination with tenecteplase can further enhance neurological recovery in patients remains unreported. Based on the above discussion, this study aims to investigate the efficacy and safety of combining tenecteplase with HUK in the treatment of AIS.

Eligibility

Min Age: 18 Years

Inclusion Criteria7

Age ≥ 18 year;
Acute ischemic stroke confirmed by neuroimaging;
The time from last known well to treatment is within 4.5 hours;
NIHSS ≥ 6 at randomization;
Received intravenous tenecteplase (0.25mg/kg);
First stroke onset or past stroke without obvious neurological deficit (mRS≤1);
Signed informed consent.

Exclusion Criteria8

Planed for endovascular treatment;
Use of Edaravone Injection, Edaravone Dexborneol Injection, Butylphthalide Injection or Capsules after the onset of the current episode；
Prior use of ACE inhibitors within a period less than 5 half-lives before the intended administration of Urinary Kallidinogenase for Injection；
Pregnancy；
Allergy to the investigational drug(s)；
Comorbidity with other serious diseases;
Participating in other clinical trials within 3 months;
Patients not suitable for the study considered by researcher.