Phase 2 Stroke Trial, Recruiting NCT07084012 Sponsor: Shenzhen Wingor Biotechnology Co., Ltd. Condition: Stroke
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Phase 2 Stroke Trial, Recruiting

NCT07084012
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults between 18 and 75 years old, of any gender
  • People who have been diagnosed with an acute ischemic stroke (a stroke caused by a blocked blood vessel in the brain)
  • People whose stroke symptoms began no more than 72 hours ago
  • People whose stroke affects the front part of the brain's blood supply (called the anterior circulation)
  • People who had little to no disability before this stroke, based on a standard disability rating scale
  • People whose stroke is rated as moderate in severity on a standard medical stroke scale, and who are not deeply unconscious
  • People for whom the patient themselves, or their legal guardian, has signed a consent form to participate

Who may not be able to join:

  • People who have had, or are planned to have, clot-dissolving treatment or a procedure to remove a clot for this stroke
  • People with a history of epilepsy (unless it is a type that no longer requires medication), Parkinson's disease, Alzheimer's disease, severe depression, or other conditions the trial doctor considers would interfere with participation
  • People who have any type of bleeding in or around the brain (small spots of bleeding may be considered on a case-by-case basis by the trial doctor)
  • People whose brain scans show a very large area of stroke damage or a significant shift of brain structures, where the trial doctor considers surgery likely or the outlook poor
  • People who have a brain tumour or a history of any cancer
  • People whose liver or kidney function falls outside acceptable levels on blood tests taken during the screening period
  • People with a history of serious heart or blood vessel disease that the trial doctor considers unsuitable for participation
  • People with a serious active infection, such as blood poisoning, septic shock, or severe pneumonia
  • People who have received high-dose steroid medication or immune-suppressing drugs within the 14 days before starting the trial drug, or during the trial
  • People who have consumed more than an average of 2 standard units of alcohol per day over the past year (where 1 unit equals 200 mL of regular beer, 25 mL of spirits, or 85 mL of wine)
  • Women who are pregnant or breastfeeding, or anyone unwilling to use reliable contraception throughout the study, or anyone planning to donate sperm or eggs, or planning a pregnancy during the study
  • People who have taken part in another interventional clinical trial in the past 3 months, or who have previously received any cell-based therapy (other than a blood transfusion)
  • People the trial doctor considers unsuitable for any other reason, including concerns about cooperation with the study or abnormal test results

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 86-0755-66835786

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Shenzhen Wingor Biotechnology Co., Ltd.
Registry
ClinicalTrials.gov
Start date
27 August 2025
Est. completion
5 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The proportion of subjects with an mRS score of 0-2 at different follow-up visits after treatment.; The proportion of subjects with an NIHSS improvement of ≥4 points at different follow-up visits after treatment; Changes in NIHSS score from baseline at different follow-up visits after treatment; Trends in the distribution of mRS scores (0-6) at different follow-up visits after treatment; The proportion of subjects with a Barthel Index (BI) score of ≥95 at different follow-up visits after treatment; Changes in Fugl-Meyer Motor Function Assessment Scale score from baseline at different follow-up...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov