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Human Placenta-derived 3D Mesenchymal Stem Cells(Guojianqingke) (3D MSC - QK01)

3 de junio de 2026 actualizado por: Zhao Dong, MD, Chinese PLA General Hospital

A Phase I/IIa Clinical Trial on the Safety, Tolerability, and Preliminary Efficacy of Human Placental-Derived 3D Mesenchymal Stem Cell Injection Administered Via the Intravenous Route in Patients With Acute Ischemic Stroke (AIS): A Randomized, Double-Blind, Placebo-Controlled Study

This is a Phase I/IIa clinical trial evaluating human placental-derived 3D mesenchymal stem cell (MSC) injection in patients with acute ischemic stroke (AIS). Phase I is a single-dose escalation study to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D). Phase IIa explores preliminary efficacy. Each participant undergoes screening (up to 72 hours before treatment), a single-day treatment period, and follow-up for up to 720 days (24 months).

Descripción general del estudio

Descripción detallada

This study consists of two sequential phases:

Phase I (Dose Escalation): A single ascending dose design to evaluate safety and tolerability of intravenous human placental-derived 3D MSC injection in AIS patients, and to establish the MTD and RP2D.

Phase IIa (Expansion): A randomized, double-blind, placebo-controlled evaluation of preliminary efficacy at the RP2D.

Study Duration: Screening within 72 hours of stroke onset; single-day treatment; follow-up visits through Day 720.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

24

Fase

  • Fase 2
  • 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

Ubicaciones de estudio

      • Beijing, Porcelana
        • Reclutamiento
        • Chinese People's Liberation Army General Hospital, First Medical Center
        • Contacto:

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:

  1. Age ≥18 years and ≤80 years; any gender
  2. Body weight 45-90 kg
  3. Diagnosed with acute ischemic stroke, with onset between 6 and 72 hours (inclusive) prior to enrollment; received thrombolysis or not planned for thrombolysis and no planned thrombectomy
  4. NIHSS score 6-20, with NIHSS item 1a (Level of Consciousness) <2
  5. Participant or legally authorized representative able to understand and provide written informed consent

Exclusion Criteria:

  1. Significant pre-stroke disability (pre-stroke modified Rankin Scale [mRS] score ≥2);
  2. History of intracerebral hemorrhage, subarachnoid hemorrhage, or hemorrhagic transformation after this ischemic stroke (imaging re-evaluation before planned dosing shows new bleeding within the infarct area accompanied by neurological deterioration [e.g., NIHSS total score increased ≥4 points from admission], judged by the investigator as unsuitable for clinical trial participation); or presence of cerebrovascular malformation, multiple sclerosis, severe traumatic brain injury history, encephalitis, or other conditions causing stroke-like symptoms
  3. Uncontrolled systemic diseases, including but not limited to: hypertension (systolic BP >180 mmHg and/or diastolic BP ≥120 mmHg), diabetes (diabetic acute complications such as ketoacidosis, hyperosmolar hyperglycemic state, lactic acidosis, or hypoglycemic coma within 3 months, or difficult-to-control diabetes [blood glucose >16.8 mmol/L or <2.8 mmol/L]), renal disease (eGFR <30 mL/min/1.73m²), hepatic failure (Child-Pugh Class C), severe heart failure (NYHA Class IV), severe chronic respiratory disease
  4. History of seizure (except secondary epilepsy not currently requiring drug treatment)
  5. History of brain tumor or malignancy within the past 5 years, including concurrent second primary malignancy, except: a) radically excised non-melanoma skin cancer; b) radically treated cervical carcinoma in situ; c) radically treated papillary thyroid carcinoma; d) radically treated localized prostate cancer; e) radically treated ductal carcinoma in situ of the breast
  6. History of any of the following:

    1. Active or uncontrolled autoimmune disease (e.g., antiphospholipid antibody syndrome)
    2. Protein C or protein S deficiency
    3. Sickle cell anemia
    4. Deep vein thrombosis
    5. Pulmonary embolism
    6. Cerebrovascular malformation (e.g., moyamoya disease)
  7. Any concomitant disease or physical condition (e.g., severe arthritis, amputation, blindness, severe disability from prior stroke) that, in the investigator's judgment, would significantly interfere with accurate assessment of mRS, NIHSS, or BI scores
  8. Major surgery within the past 30 days (e.g., thoracotomy, cardiac surgery, abdominal surgery, intracranial surgery)
  9. Currently severe illness, including:

    1. Severe heart failure (NYHA Class III-IV)
    2. Severe febrile illness (any fever within 14 days before dosing requiring systemic anti-infective treatment)
    3. Primary or secondary immunodeficiency disease, or long-term or recent high-dose immunosuppressant or systemic corticosteroid therapy before screening
    4. Hemorrhagic disorder or bone marrow transplantation
    5. Any comorbidity that the investigator believes may shorten survival or limit ability to complete the study
    6. Uncontrolled depression affecting daily life before stroke, dementia that may affect clinical assessment, or other neurological or psychiatric disorders that the investigator believes may affect study assessment
  10. Uncontrolled active infection; or systemic anti-infective treatment within 7 days before dosing that the investigator assesses may shortly convert to uncontrolled active infection
  11. Organ function meeting any of the following:

    Hematology:

    Absolute neutrophil count (ANC) <1.0×10⁹/L Platelets (PLT) <75×10⁹/L Hemoglobin (Hb) <80 g/L

    Hepatic/Renal Function:

    Alanine aminotransferase (ALT) >2.5×ULN Aspartate aminotransferase (AST) >2.5×ULN Total bilirubin (TBIL) >1.5×ULN Creatinine >1.5×ULN

    Coagulation:

    Phase I: Not receiving anticoagulant or antithrombotic therapy: PT and APTT >1.25×ULN, INR >1.4; Receiving anticoagulant or antithrombotic therapy: PT and APTT >1.5×ULN, INR >3.0 Phase IIa: Not receiving anticoagulant therapy: APTT >2.0×ULN or PT >2.0×ULN; Receiving anticoagulant therapy: judged by investigator to have severe bleeding risk

  12. Clinically significant uncorrected electrolyte disturbances (e.g., hyperkalemia, hypernatremia) that the investigator believes may affect study assessment
  13. Unable to undergo head CT/MRI for any reason (e.g., cardiac pacemaker, metal implants, claustrophobia)
  14. History of drug abuse or alcohol abuse within the past year
  15. Allergy to bovine or porcine products, human serum albumin products, or known allergy to gentamicin
  16. Participation in another investigational drug, device study, or stem cell/immune cell therapy within 3 months before treatment
  17. History of blood transfusion or vaccination with attenuated/live vaccine within 3 months before screening
  18. Pregnant or lactating women; or participants with pregnancy plans during the study period, or unwilling to use effective contraception; or females of childbearing potential with positive pregnancy test; or female participants on long-term oral contraceptives (continuous use >30 days)
  19. Other reasons deemed by the investigator as unsuitable for participation or inability to complete study procedures (e.g., lack of willingness)

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 Placental-Derived 3D Mesenchymal Stem Cell Injection

This product is administered by intravenous infusion. The investigator will calculate the dosage based on the dose group assigned to each participant.

Preparation: Remove the product from liquid nitrogen and immediately thaw in a 37±1°C water bath. After thawing, add 40 mL of pre-cooled (2-8°C) compound electrolyte injection to the product bag and mix well.

Administration: The recommended infusion time is 30 minutes (±5 minutes) per bag.

Comparador de placebos: Cell Culture Medium (Cell-Free)

This product is administered by intravenous infusion. The investigator will calculate the dosage based on the dose group assigned to each participant.

Preparation: Remove the product from liquid nitrogen and immediately thaw in a 37±1°C water bath. After thawing, add 40 mL of pre-cooled (2-8°C) compound electrolyte injection to the product bag and mix well.

Administration: The recommended infusion time is 30 minutes (±5 minutes) per bag.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of Participants with Modified Rankin Scale (mRS) Score of 0-2
Periodo de tiempo: Day 90 post-treatment

Functional outcome assessed by the Modified Rankin Scale (mRS), a validated clinician-reported 7-point ordinal scale (minimum = 0, maximum = 6). Higher scores indicate worse functional outcome (0 = no symptoms, 6 = death). A score of 0-2 indicates functional independence. Assessment conducted by a trained, blinded neurologist via structured interview using the standardized mRS questionnaire.

% of participants with mRS score 0-2

Day 90 post-treatment

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of Participants with mRS Score 0-2 at Day 28
Periodo de tiempo: Day 28 post-treatment

Functional outcome assessed by the Modified Rankin Scale (mRS), a validated clinician-reported 7-point ordinal scale (minimum = 0, maximum = 6). Higher scores indicate worse functional outcome (0 = no symptoms, 6 = death). A score of 0-2 indicates functional independence. Assessment conducted by a trained, blinded neurologist via structured interview using the standardized mRS questionnaire.

% of participants with mRS score 0-2

Day 28 post-treatment
Proportion of Participants with mRS Score 0-2 at Day 180
Periodo de tiempo: Day 180 post-treatment

Functional outcome assessed by the Modified Rankin Scale (mRS), a validated clinician-reported 7-point ordinal scale (minimum = 0, maximum = 6). Higher scores indicate worse functional outcome (0 = no symptoms, 6 = death). A score of 0-2 indicates functional independence. Assessment conducted by a trained, blinded neurologist via structured interview using the standardized mRS questionnaire.

% of participants with mRS score 0-2

Day 180 post-treatment
Proportion of Participants with mRS Score 0-2 at Day 270
Periodo de tiempo: Day 270 post-treatment

Functional outcome assessed by the Modified Rankin Scale (mRS), a validated clinician-reported 7-point ordinal scale (minimum = 0, maximum = 6). Higher scores indicate worse functional outcome (0 = no symptoms, 6 = death). A score of 0-2 indicates functional independence. Assessment conducted by a trained, blinded neurologist via structured interview using the standardized mRS questionnaire.

% of participants with mRS score 0-2

Day 270 post-treatment
Proportion of Participants with mRS Score 0-2 at Day 360
Periodo de tiempo: Day 360 post-treatment

Functional outcome assessed by the Modified Rankin Scale (mRS), a validated clinician-reported 7-point ordinal scale (minimum = 0, maximum = 6). Higher scores indicate worse functional outcome (0 = no symptoms, 6 = death). A score of 0-2 indicates functional independence. Assessment conducted by a trained, blinded neurologist via structured interview using the standardized mRS questionnaire.

% of participants with mRS score 0-2

Day 360 post-treatment

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of Dose-Limiting Toxicity (DLT)
Periodo de tiempo: Throughout the dose-escalation phase (Phase I only)

Dose-Limiting Toxicity assessed by clinical evaluation and laboratory monitoring according to predefined criteria based on NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. DLT is defined as: Grade ≥3 non-hematologic toxicity, Grade ≥4 hematologic toxicity lasting >7 days, or any toxicity requiring dose delay >14 days. Assessment includes: physical examination, vital signs monitoring, hematology panel, blood chemistry, and coagulation tests.

% of participants with DLT events

Throughout the dose-escalation phase (Phase I only)
Incidence of Serious Adverse Events (SAE)
Periodo de tiempo: From first dose through Day 720

Serious Adverse Events assessed by clinical monitoring, laboratory evaluation, and radiographic imaging according to NCI-CTCAE version 5.0 and ICH E2A regulatory definitions. SAE includes: death, life-threatening event, hospitalization, disability/incapacity, congenital anomaly, or other medically important event. Assessment tools include: clinical examination, automated vital signs monitors, laboratory analyzers, and CT/MRI imaging.

% of participants with SAEs

From first dose through Day 720

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 (Actual)

1 de junio de 2026

Finalización primaria (Estimado)

30 de diciembre de 2027

Finalización del estudio (Estimado)

1 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

29 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

3 de junio de 2026

Publicado por primera vez (Actual)

9 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de junio de 2026

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

3 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)?

INDECISO

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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