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A Phase I Trial of Umbilical Cord Mesenchymal Stromal Cells for Acute Ischemic Stroke

1 de junio de 2026 actualizado por: BOE Technology Group Co., Ltd.

A Phase I Clinical Trial to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Human Umbilical Cord-derived Mesenchymal Stromal Cell Injection in Patients With Acute Ischemic Stroke (AIS)

Study Methods: The trial consists of two phases, both including a placebo control.

Phase Ia (single-dose, dose-escalation): Three dose groups (low, medium, high) are set. This is a multicenter, randomized, double-blind, placebo-controlled, single-dose, dose-escalation trial. Dose escalation to the next level is permitted only after safety assessment at 28 days post-dose in the previous group.

Phase Ib (multiple-dose): Based on Phase Ia results, two dose groups will be selected. The product is administered on Day 0, Day 7, and Day 14 (3 doses total). The trial remains randomized, double-blind, and placebo-controlled.

Descripción general del estudio

Descripción detallada

Objective of this study: To preliminarily evaluate the safety and efficacy of human umbilical cord-derived mesenchymal stromal cell injection in the treatment of AIS.

Study methods: This trial is divided into two phases, both including a placebo control.

Phase I (Ia): A multicenter, randomized, double-blind, placebo-controlled, single-dose, dose-escalation trial. Three dose groups are set: low dose (5.0×10⁷ cells), medium dose (1.0×10⁸ cells), and high dose (2.0×10⁸ cells). The low-dose group enrolls 3-6 participants (all receiving the investigational product, with the first of the first 3 participants as a sentinel). The medium- and high-dose groups each enroll 8 participants (2 sentinels receiving the investigational product, and the remaining 6 randomized in a 2:1 ratio to the investigational product or placebo group). Phase Ia plans to enroll 19-22 participants. Dose escalation to the next dose group is permitted only after all participants in the previous dose group have completed dosing and been observed for at least 28 days with a favorable safety assessment.

Phase Ib: A multicenter, randomized, double-blind, placebo-controlled, dose-escalation, multiple-dose trial. Based on the results of Phase Ia, two dose groups will be selected. The initial plan is to administer the product on Day 0, Day 7, and Day 14 (3 doses in total). Each dose group enrolls 8 participants (6 receiving the investigational product, 2 receiving placebo), for a total of 16 participants. Escalation to the next higher dose group is permitted only after all participants in the previous dose group have completed the three doses and been observed for at least 28 days with a favorable safety assessment.

Study duration: 720 days

Tipo de estudio

Intervencionista

Inscripción (Estimado)

35

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Yongjun Wang Chief Physician, Professor
  • Número de teléfono: 010-59978538
  • Correo electrónico: yongjunwang111@aliyun.com

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana
        • Beijing Tiantan Hospital, Capital Medical University
        • Contacto:
          • Shu ya Li Chief Physician
          • Número de teléfono: +86 13601367028
          • Correo electrónico: shuyali85@163.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Age ≥18 years, both genders included.
  • Clinical diagnosis of anterior circulation ischemic stroke, and able to receive the investigational product within 48 hours after the onset of stroke symptoms.
  • National Institutes of Health Stroke Scale (NIHSS) score of 6-20 (inclusive), with a score of <2 on item Ia of the NIHSS.
  • Pre-stroke modified Rankin Scale (mRS) score ≤1.
  • The participant voluntarily agrees to participate in this study, signs the informed consent form personally or via a legal guardian, and has good compliance.

Exclusion Criteria:

  • Planned or already performed thrombectomy for the current stroke.
  • Treatment with neuroprotective agents after the current stroke.
  • History of cerebral hemorrhage, subarachnoid hemorrhage, or hemorrhagic transformation after the current ischemic stroke, and judged by the investigator to be unsuitable for participation in the clinical trial.
  • Uncontrolled systemic diseases, including but not limited to: hypertension (systolic blood pressure >160 mmHg and/or diastolic blood pressure ≥100 mmHg), diabetes mellitus (acute diabetic complications such as ketoacidosis, hyperglycemic hyperosmolar state, lactic acidosis, or hypoglycemic coma within the past 3 months, or glycated hemoglobin >8.5%, or poorly controlled blood glucose [blood glucose >16.8 mmol/L or <2.8 mmol/L]), renal disease (eGFR <30 mL/min), liver failure (Child-Pugh Class C), severe heart failure (New York Heart Association [NYHA] Class IV), severe chronic respiratory disease.
  • Organ function meeting any one or more of the following criteria:

    1. Absolute neutrophil count (ANC) <1.5×10⁹/L, platelet count (PLT) <100×10⁹/L, hemoglobin (Hb) <90 g/L;
    2. Aspartate aminotransferase (AST) >2.5× upper limit of normal (ULN) and/or alanine aminotransferase (ALT) >2.5×ULN, serum total bilirubin (TBIL) >1.5×ULN;
    3. Creatinine (Cr) >1.5×ULN;
    4. For patients not receiving anticoagulant or antithrombotic therapy: international normalized ratio (INR) >1.7 or activated partial thromboplastin time (APTT) >1.25×ULN; for patients receiving anticoagulant or antithrombotic therapy: INR >3.0 or APTT >1.5×ULN.
  • Diagnosis of immunodeficiency disease, or long-term use of immunosuppressants or systemic corticosteroids at high doses within a short period before screening.
  • Epilepsy, Alzheimer's disease, Parkinson's disease, severe depression, or other neurological or psychiatric disorders that, in the investigator's opinion, could affect the participant's ability to participate in the trial or interfere with study assessments.
  • Presence of autoimmune diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus, etc.).
  • Inability to undergo cranial CT/MRI examination for any reason (e.g., metallic implants such as cardiac pacemakers, claustrophobia, etc.).
  • Participation in another clinical trial of an investigational drug within 3 months before screening.
  • Pregnancy, breastfeeding, planned pregnancy, or inability to use effective contraceptive measures.
  • Any other condition that, in the investigator's judgment, makes the participant unsuitable for inclusion in this study.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Human Umbilical Cord Mesenchymal Stromal Cells Injection(low-dose group)
5.0×10^7 cells,Single intravenous infusion
the first phase (Phase Ia) is a single-dose administration
the second phase (Phase Ib) is a multiple-dose administration.
Experimental: Human Umbilical Cord Mesenchymal Stromal Cells Injection(medium-dose group)
1.0×10^8 cells,Single intravenous infusion
the first phase (Phase Ia) is a single-dose administration
the second phase (Phase Ib) is a multiple-dose administration.
Experimental: Human Umbilical Cord Mesenchymal Stromal Cells Injection(high-dose group)
2.0×10^8 cells,Single intravenous infusion
the first phase (Phase Ia) is a single-dose administration
the second phase (Phase Ib) is a multiple-dose administration.
Comparador de placebos: Placebo of Human Umbilical Cord Mesenchymal Stromal Cells Injection(medium-dose group)
1.0×10^8 cells,Single intravenous infusion
Placebo refers to a cell-free product, whose packaging, storage conditions, expiration date, and method of administration remain consistent with those of the investigational drug.
Comparador de placebos: Placebo of Human Umbilical Cord Mesenchymal Stromal Cells Injection(high-dose group)
2.0×10^8 cells,Single intravenous infusion
Placebo refers to a cell-free product, whose packaging, storage conditions, expiration date, and method of administration remain consistent with those of the investigational drug.
Experimental: Human Umbilical Cord Mesenchymal Stromal Cells Injection 1
Based on the results from the Phase Ia trial, dose group 1 will be considered for the Phase Ib trial.For multiple dosing, it is initially planned to administer the injection once on Day 0, Day 7, and Day 14, for a total of 3 doses.
the first phase (Phase Ia) is a single-dose administration
the second phase (Phase Ib) is a multiple-dose administration.
Experimental: Human Umbilical Cord Mesenchymal Stromal Cells Injection 2
Based on the results from the Phase Ia trial, dose group 2 will be considered for the Phase Ib trial.For multiple dosing, it is initially planned to administer the injection once on Day 0, Day 7, and Day 14, for a total of 3 doses.
the first phase (Phase Ia) is a single-dose administration
the second phase (Phase Ib) is a multiple-dose administration.
Comparador de placebos: Placebo of Human Umbilical Cord Mesenchymal Stromal Cells Injection 1
Based on the results from the Phase Ia trial, dose group 1 will be considered for the Phase Ib trial.For multiple dosing, it is initially planned to administer the injection once on Day 0, Day 7, and Day 14, for a total of 3 doses.
Placebo refers to a cell-free product, whose packaging, storage conditions, expiration date, and method of administration remain consistent with those of the investigational drug.
Comparador de placebos: Placebo of Human Umbilical Cord Mesenchymal Stromal Cells Injection 2
Based on the results from the Phase Ia trial, dose group 2 will be considered for the Phase Ib trial.For multiple dosing, it is initially planned to administer the injection once on Day 0, Day 7, and Day 14, for a total of 3 doses.
Placebo refers to a cell-free product, whose packaging, storage conditions, expiration date, and method of administration remain consistent with those of the investigational drug.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Incidence of DLT (Dose-Limiting Toxicity) events;
Periodo de tiempo: Day28
Day28
All adverse events/serious adverse events during the trial;
Periodo de tiempo: 2year
2year
All-cause mortality
Periodo de tiempo: Day90、Day180、Day360
Day90、Day180、Day360

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of participants with an Modified Rankin Scale (mRS) score of 0-2
Periodo de tiempo: Day 30, Day90, Day180, Day360

The modified Rankin Scale (mRS) is a widely used clinical outcome measure that assesses the degree of disability or dependence in the daily activities of patients who have suffered a stroke or other neurological conditions. It is a simple, 7-level ordinal scale ranging from 0 to 6:

0 - No symptoms at all.

  1. - No significant disability: able to perform all usual activities despite some symptoms.
  2. - Slight disability: unable to carry out all previous activities but able to look after own affairs without assistance.
  3. - Moderate disability: requires some help but able to walk without assistance.
  4. - Moderately severe disability: unable to walk or attend to bodily needs without assistance.
  5. - Severe disability: bedridden, incontinent, requiring constant nursing care.
  6. - Dead.

A higher score indicates more severe disability. The mRS is the most common primary endpoint in acute stroke clinical trials, with a score of 0-2 at 90 days often defined as a "good outcome.

Day 30, Day90, Day180, Day360
Proportion of participants with a ≥4-point improvement in National Institutes of Health Stroke Scale (NIHSS) score from baseline
Periodo de tiempo: Day 7, Day 14, Day 30, Day 90, Day 180, Day 360
The National Institutes of Health Stroke Scale (NIHSS) is a standardized tool used to objectively quantify the severity of neurological deficits in patients with stroke. It consists of 15 items, including assessments of consciousness, eye movements, visual fields, facial palsy, motor and sensory function, language, speech, and neglect. Each item is scored, with a total score ranging from 0 to 42. Higher scores indicate more severe neurological impairment. The NIHSS is widely used in clinical practice and research to evaluate stroke severity, guide treatment decisions, and predict patient outcomes.
Day 7, Day 14, Day 30, Day 90, Day 180, Day 360
Change from baseline in National Institutes of Health Stroke Scale(NIHSS) score
Periodo de tiempo: Day 7, Day 14, Day 30, Day 90, Day 180, Day 360
Day 7, Day 14, Day 30, Day 90, Day 180, Day 360
Proportion of participants with a Barthel Index ≥95
Periodo de tiempo: Day 30, Day 90, Day180, Day360
The Barthel Index (BI) is a standardized ordinal scale used to measure a person's performance in activities of daily living (ADL). It assesses 10 basic functions, including feeding, bathing, grooming, dressing, bowel and bladder control, toilet use, transfers (e.g., bed to chair), mobility, and stair climbing. Each item is scored based on the amount of physical assistance required, with total scores typically ranging from 0 to 100 (or 0-20 in some versions). It is widely used in geriatrics, rehabilitation, and stroke research to evaluate functional independence and track changes over time.A higher Barthel Index score indicates greater functional independence (less need for assistance), while a lower score reflects greater disability and dependency. For example, a score of 100 means the patient is fully independent in basic ADL.
Day 30, Day 90, Day180, Day360
Change from baseline in the Fugl-Meyer Motor Function Assessment Scale score
Periodo de tiempo: Day 30, Day90, Day180, Day 360
The Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based impairment index widely recognized as a gold standard scale for evaluating sensorimotor recovery in patients with post-stroke hemiplegia. A higher FMA score indicates better motor function and less impairment, reflecting more positive outcomes in stroke recovery. For example, the motor domain score ranges from 0 (complete hemiplegia) to 100 (normal motor performance). The total FMA score is therefore a direct measure of functional recovery: the higher the score, the greater the improvement in sensorimotor function following stroke.
Day 30, Day90, Day180, Day 360
Change from baseline in objective imaging findings (CT/MRI)
Periodo de tiempo: Day 90
Day 90

Otras medidas de resultado

Medida de resultado
Periodo de tiempo
mmunogenicity: Human Leukocyte Antigen (HLA) antibodies.
Periodo de tiempo: Within 60 minutes before the first dose, and at 14 days, 30 days, and 90 days after the start of the first dose administration.
Within 60 minutes before the first dose, and at 14 days, 30 days, and 90 days after the start of the first dose administration.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

30 de junio de 2026

Finalización primaria (Estimado)

30 de marzo de 2028

Finalización del estudio (Estimado)

30 de noviembre de 2029

Fechas de registro del estudio

Enviado por primera vez

22 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

1 de junio de 2026

Publicado por primera vez (Actual)

5 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

1 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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