NCT06612710RecruitingPhase 1
The Safety and Efficacy of NouvSoma001 in Ischemic Stroke
An Open-label Exploratory Clinical Trial to Assess the Safety and Efficacy of NouvSoma001 in the Treatment of Ischemic Stroke
Source: ClinicalTrials.gov · Last updated 21 Jan 2026
Brief summary (registry, in English)
This is a single-center, randomized, open-label, placebo-controlled, dose-escalation trial. The objective of this research is to evaluate the safety, tolerability, and preliminary efficacy of intravenous administration of human-induced neural stem cell-derived extracellular vesicles (NouvSoma001) in the treatment of ischemic stroke.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 69 (estimated)
- First submitted
- 22 Sept 2024
- Start date
- 30 Nov 2025
- Primary completion date
- 30 Dec 2026
- Lead sponsor
- Wei Wang
- Diseases
- Stroke
- NCT number
- NCT06612710
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 69
- From 30 Nov 2025 to the primary completion date, 30 Dec 2026
- 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
- Patients with alcohol addiction or those testing positive for drug abuse.
Other illness
- CT indicates intracranial hemorrhage, including hemorrhagic stroke, epidural hematoma, subdural hematoma, intraventricular hemorrhage, subarachnoid hemorrhage, or hemorrhagic transformation.
- Patients with Alzheimer's disease, Parkinson's syndrome, or other neurodegenerative disorders.
- Evidence of brain tumors, epilepsy, or a history of traumatic brain injury.
- Presence of non-vascular diseases causing white matter lesions, such as carbon monoxide poisoning, multiple sclerosis, or adrenoleukodystrophy.
- Persistent systemic infection, severe local infection, or ongoing use of immunosuppressants.
- Patients with malignant diseases or an expected survival of less than 5 years.
- Significant hearing or vision impairments, language disorders, or claustrophobia that would hinder cooperation with neuropsychological assessments and MRI examinations.
- Patients with a history of severe allergies or known allergy to human biological products.
Lab values
- Severe liver, renal, cardiac, or pulmonary insufficiency, hematologic disorders, or malignant tumors (Liver insufficiency is defined as ALT or AST levels greater than 1.5 times the upper normal limit; renal insufficiency is defined as serum creatinine levels greater than 1.5 times the upper normal limit).
Other
- Rapid spontaneous neurological improvement during the screening period, defined as a reduction of NIHSS score by ≥ 8 points from symptom onset to the first administration.
- Contraindications to MRI.
- Patients unable to comply with follow-up requirements during the study.
- Pregnant or breastfeeding women, and those planning to conceive during the trial period.
- Participation in other clinical trials within the past 3 months.
- Patients considered unsuitable for participation by the investigator.
Who the study is looking for
- The age of the recruiters ranged from 18 to 75 years.
- Clinical diagnosis of ischemic stroke, the time of stroke onset is known, and the onset occurred no more than 7 days before enrollment.
- Magnetic resonance imaging (MRI) or computed tomography (CT) findings consistent with ischemic stroke.
- At the time of enrollment, the NIHSS score is between 6 and 20; additionally, there is at least one limb with muscle strength ≤ Grade 3.
- Patients who have the mental capacity to understand and participate in the study.
- Informed consent was obtained from patients or their legal representatives.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Tongji Hospital affiliated to Tongji Medical College of Huazhong University ofScience and Technology Coordinator of this site? Confirm its status | Wuhan | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.