Efficacy and Safety of Interleukin-6 Receptor Inhibitor Combined With Endovascular Treatment in Patients With Acute Posterior Circulation Large Vessel Occlusion Stroke

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorCapital Medical University

About this trial

This is an investigator-initiated phase III clinical trial employing a randomized, double-blind, placebo-controlled design. The primary objective of this study is to investigate the efficacy and safety of an interleukin-6 inhibitor (tocilizumab) combined with endovascular therapy in patients with acute posterior circulation large-vessel occlusion stroke.

Eligibility criteria

Qualifiers

Age 18 years or older, of either sex;

Acute ischemic stroke caused by occlusion of the basilar artery;

Decide to undergo emergency endovascular treatment;

Time from stroke onset to groin puncture within 24 hours;

Disqualifiers

Intracerebral hemorrhage, epidural hematoma, subdural hematoma, intraventricular hemorrhage, or subarachnoid hemorrhage;

Pre-stroke modified Rankin scale (mRS) score >1;

Known allergy to tocilizumab or excipients;

Known allergy to iodinated contrast agents;

Trial design

Treatments tested in this trial

  • Tocilizumab
  • Placebo

Treatment groups

348 Participants
are divided into 2 treatment groups

Sponsors and collaborators