Tenecteplase (TNK) in the Treatment of Intracerebral Hemorrhage (ICH)

Launched by GAURAV GUPTA, MD · Nov 18, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a treatment called Tenecteplase (TNK) for patients who have experienced an intracerebral hemorrhage (ICH), which is a type of bleeding in the brain. The goal is to see if TNK is safe and effective when given directly into the area of bleeding, compared to the current standard treatment, which is another drug called rtPA. By breaking down blood clots, these treatments can help improve health outcomes for patients suffering from this serious condition.

To be eligible for the trial, patients need to be between 18 and 80 years old and must have had a brain bleed within the last 24 hours. They should have specific types of ICH and meet certain health criteria. If someone participates, they will undergo a surgical procedure similar to what would normally be done for their condition, but instead of receiving rtPA, they will receive TNK. The trial is not yet recruiting participants, but it aims to provide valuable information about a potentially better treatment for ICH.

Gender

ALL

Eligibility criteria

• • Inclusion Criteria
• • Patient/legally authorized representative has signed the Informed Consent Form.
• • Ability to comply with the study protocol, in the investigator's judgment.
• • Patients 18 to 80 years of age with an ICH had occurred within 24 hours before admission.
• • Spontaneous supratentorial (basal ganglia, thalamus, lobar) ICH ≥30 mL measured utilizing the ABC/2 method.
• • Subjects with a GCS score of 5-14.
• • NIHSS ≥6.
• • Stability CT scan done at least 6 hours after baseline CT showing clot stability (growth \<5 mL as measured by ABC/2 method). If the hematoma volume measured on the stability CT scan increases by 5 mL or more, a second stability CT scan will be performed 12 hours later.
• • Sustained systolic blood pressure (SBP) \<180 mm Hg for six hours recorded closest to the time of drug administration.
• • Symptoms must be present less than 24 hours prior to baseline CT scan.
• • Baseline Rankin score of 0 or 1.
• • Exclusion Criteria
• • Presence of infratentorial parenchymal bleeding.
• • Presence of a hemorrhage extending to the midbrain.
• • An unknown time of onset or the symptoms onset more than 24 hours prior to admission.
• • Pregnancy.
• • Inability to obtain written informed consent from subject or legal representative.
• • Sustained SBP \>180 mm Hg for six hours recorded closest to the time of drug administration.
• • Age \<18 and \>80 years.
• • Radiological evidence of arterio-venous malformation, aneurysm, amyloid angiopathy, Moyamoya disease, hemorrhagic conversion of an ischemic stroke, recurrent hemorrhage in the same location within the past 365 year or unstable mass as a source for the ICH.
• • Evidence of coagulopathy (international normalized ratio \>1.3; platelet count \<100 ,000 or platelet dysfunction P2Y-12 \>250) or known clotting disorder.
• • Bilateral fixed, dilated pupils indicating irreversible impaired brain stem function with GCS ≤4.
• • Patients with severe ICH and IVH who require an external ventricular drain (EVD) placement for cerebrospinal fluid (CSF) diversion or separate intraventricular thrombolysis.
• • Inability to maintain INR less than 1.3.
• • Use of anticoagulants prior to symptom onset and subjects requiring long-term anticoagulants (the reversal is permitted if the patient can tolerate the short-term risk of reversal).
• • Use of Dabigatran, Apixaban, and/or Rivaroxaban (or a similar medication from the similar medication class) prior to symptom onset.
• • Internal bleeding (GI, renal, respiratory etc).
• • Mechanical heart valve (Bioprosthetic heart valve is permitted).
• • Known risk for embolization, including history of left heart thrombus, mitral stenosis with atrial fibrillation, acute pericarditis, or subacute bacterial endocarditis (atrial fibrillation without mitral stenosis is permitted).
• • Allergy or sensitivity to TNKase.
• • Participation in a concurrent clinical trial.
• • Serious illness (advanced stage which can interfere with the outcome).
• • The patient is unstable and would not benefit from a surgical intervention.
• • GCS score of 3-4 and 15 (to ensure patient safety and study feasibility).
• • Historical mRS score of 2-6 (at admission).
• • Symptomatic tract hemorrhage or a tract hemorrhage more than 5 mm.