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NCT07449910Not yet recruitingPhase 2/3

Safety and Efficacy of Baricitinib After Endovascular Treatment in Acute Anterior Circulation Large Vessel Occlusion: A Multicenter, Randomized Controlled Clinical Trial

Safety and Efficacy of Baricitinib Combined With Acute Large Vessel Occlusion Recanalization : A Multicenter, Randomized Controlled Clinical Trial

Source: ClinicalTrials.gov · Last updated 4 Mar 2026

Brief summary (registry, in English)

The primary purpose of this study is to evaluate the efficacy and safety of Baricitinib combined with endovascular therapy in patients with acute anterior circulation large vessel occlusion, to address futile recanalization with priority, and to elucidating the mechanism of JAK/STAT pathway inhibition on neuroprotection and inflammatory regulation.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
750 (estimated)
First submitted
27 Feb 2026
Start date
Mar 2026
Primary completion date
Aug 2027
Lead sponsor
The First Affiliated Hospital of University of Science and Technology of China
Diseases
Stroke
NCT number
NCT07449910

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 750
  • From Mar 2026 to the primary completion date, Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Systolic blood pressure \>185 mmHg or diastolic blood pressure \>110 mmHg, and unable to be controlled by oral antihypertensive drugs.
  • Previous history of diagnosed viral hepatitis and tuberculosis.

Other illness

  • Intracranial hemorrhage confirmed by CT or MRI.
  • Allergic to contrast agents.
  • Allergic to baricitinib or having contraindications for using baricitinib.
  • Recent history of using other JAK inhibitors or potent immunosuppressants, including but not limited to the combined use with potent immunosuppressive drugs such as azathioprine, tacrolimus, tofacitinib and fedratinib, etc. Tortuous arteries make the thrombectomy device unable to reach the target blood vessel.

Lab values

  • Genetic or acquired bleeding diathesis, lack of anticoagulant factors or having taken oral anticoagulants and INR \>1.7.
  • Hemoglobin value \<8g/L.

Age

  • mRS score\>2 for patients \<80 years, or mRS score\>1 for those ≥80 years before onset.

Other

  • Pregnant or lactating women.
  • Participating in other clinical studies.

Who the study is looking for

  • Age is 18 years old or above.
  • Diagnosed as anterior circulation large vessel occlusion stroke by CTA, MRA or DSA.
  • Randomized within 24h after the onset.
  • The NIHSS score is above 5 and the ASPECT score is above 3 points while receiving imaging examination;
  • The mTICI score after endovascular treatment (EVT) is above 2b.
  • informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital of University of Science and Technology of China, Hefei, Recruiting
Coordinator of this site? Confirm its status
HefeiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.