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Phase Ⅰ/Ⅱa Trial Evaluating Intravenous hUC-MSCs Injection for Safety, Tolerability and Efficacy in Patients With POI

19 de agosto de 2026 actualizado por: Shenzhen Wingor Biotechnology Co., Ltd.

Phase Ⅰ/Ⅱa Clinical Trial to Evaluate the Safety, Tolerability and Efficacy of Intravenous Injection of Human Umbilical Cord Mesenchymal Stem Cells (hUC-MSCs) in Patients With Premature Ovarian Insufficiency (POI)

A Phase I/IIa clinical study evaluating the safety, tolerability and efficacy of intravenously administered human umbilical cord mesenchymal stem cell (hUC-MSCs) injection in patients with premature ovarian insufficiency (POI).

The primary objective of the Phase I dose-escalation stage is to assess the safety and tolerability of intravenous infusion of hUC-MSCs injection for the treatment of POI, and to determine the recommended phase II dose (RP2D) for the Phase IIa clinical trial.

The primary objective of the Phase IIa dose-expansion stage is to evaluate the efficacy of intravenous infusion of hUC-MSCs injection in POI treatment, and to generate data to support pivotal/confirmatory clinical trials.

Descripción general del estudio

Descripción detallada

Premature ovarian insufficiency (POI) is defined as ovarian dysfunction occurring in women before the age of 40, which is mainly characterized by menstrual abnormalities (amenorrhea, oligomenorrhea or polymenorrhea), elevated gonadotropin levels (FSH > 25 U/L), and fluctuating decline in estrogen levels. The incidence of POI is age-specific: 1 in 250 women develops POI before 35 years of age, and 1 in 100 women develops POI before 40 years of age. The incidence rate of POI in China is 2.8%, showing an upward trend year by year with a younger onset age.

hormone replacement therapy (HRT) relieves symptoms caused by low estrogen through estrogen supplementation. Sequential estrogen-progestogen therapy is recommended for POI patients with an intact uterus. Since patients with POI require long-term HRT, natural or nearly natural estrogens and progestogens can be selected to minimize adverse effects on the mammary gland, metabolism, cardiovascular system and other systems. Nevertheless, HRT still increases the risks of breast cancer, heart disease and stroke.

Studies have demonstrated that mesenchymal stem cells can home to ovarian stroma, regulate the balance of Th1/Th2 cytokines and the expression of endometrial natural killer cells, alleviate inflammatory responses, inhibit apoptosis of ovarian granulosa cells and reduce ovarian interstitial fibrosis, thereby improving the ovarian microenvironment. Meanwhile, these cells can secrete growth factors including VEGF, IGF-1 and HGF, promote proliferation of various ovarian cells and angiogenesis, repair ovarian structure and restore ovarian ovarian function. This study aims to evaluate the safety, tolerability and efficacy of intravenously administered hUC-MSCs in the treatment of patients with POI.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

59

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

  • Nombre: Xiaohong Wang,MD
  • Número de teléfono: +86 755 6683 5786
  • Correo electrónico: xiaohong@wingor.net

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100730
        • Reclutamiento
        • Peking Union Medical College Hospital
        • Contacto:
          • Qi Yu, Prof.
          • Número de teléfono: +86 10 6915 8621
          • Correo electrónico: yuqimd@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

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Aged 18 to 40 years at the time of signing the informed consent form (exclusive of the boundary values);
  2. Meet the diagnostic criteria specified in the Expert Consensus on Clinical Diagnosis and Treatment of Premature Ovarian Insufficiency (2023 Edition): oligomenorrhea (menstrual cycle longer than 35 days) or amenorrhea for more than 4 months, with basal serum follicle-stimulating hormone (FSH) > 25 U/L (tested on Days 2-4 of the menstrual cycle or during amenorrhea, at least twice with an interval of ≥4 weeks);
  3. Satisfy one of the following two criteria:

    1. Total number of antral follicles (AFC) with a diameter of 2-10 mm in bilateral ovaries < 5;
    2. Serum anti-Müllerian hormone (AMH) ≤ 7.85 pmol/L (equivalent to 1.1 ng/mL);
  4. Have received standardized hormone replacement therapy (HRT) at a stable dose for ≥3 months prior to drug administration with stable hormone levels, and maintain stable HRT per medical advice throughout the trial (within 24 weeks after enrollment);
  5. Have no fertility requirements;
  6. Agree to use effective contraceptive measures throughout the trial period (such as complete abstinence, condoms, cervical caps plus spermicides, intrauterine devices, etc.);
  7. Negative serum β-hCG test result during the screening period (to rule out pregnancy);
  8. Fully understand the trial information and sign the informed consent form.

Exclusion Criteria:

  1. Subjects with primary amenorrhea;
  2. Subjects with thyroid disorders (hypothyroidism/hyperthyroidism or thyroid malignant tumors) or resistant ovary syndrome (ROS);
  3. Subjects with abnormal female karyotypes (e.g., Turner syndrome, Fragile X syndrome);
  4. Positive serology tests (HBV antibody, HCV antibody, HIV antibody, syphilis). Exceptions: HBV carriers, patients with stable HBV after drug treatment (HBV DNA titer ≤500 IU/mL or copies <1000 copies/mL), and patients with cured HCV (negative HCV RNA test) may be enrolled if deemed eligible by the investigator;
  5. Subjects receiving or planning to use the following medications during the trial: oral or systemic corticosteroids, danazol, anticoagulants, Chinese herbal medicines or botanical supplements that may affect hormone levels or ovarian function;
  6. History of hypersensitivity to human serum albumin;
  7. Pregnant or breastfeeding subjects;
  8. Participation in another clinical trial within the past 3 months, or receipt of other cell therapies (excluding blood transfusion);
  9. History of malignant tumors;
  10. Subjects with contraindications or cautions for estrogen use, including known or suspected breast cancer, endometrial cancer, other known or suspected sex hormone-dependent malignancies, active venous or arterial thromboembolic diseases within the last 6 months, undiagnosed abnormal genital bleeding, severe hepatic or renal insufficiency [serum aspartate aminotransferase (AST) >3×ULN, serum alanine aminotransferase (ALT) >3×ULN, estimated glomerular filtration rate (eGFR) <60 mL/min], etc.;
  11. Uncontrolled diabetes, hypertension (>150/100 mmHg), heart disease, etc.;
  12. Any other conditions judged by the investigator to render the subject unsuitable for participation 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: Phase I, Dose Cohort 1
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, administered via intravenous infusion as a single dose on D0.
Otros nombres:
  • hUC-MSCs
Experimental: Phase I, Dose Cohort 2
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, administered via intravenous infusion as a single dose on D0.
Otros nombres:
  • hUC-MSCs
Experimental: Phase I, Dose Cohort 3
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, administered via intravenous infusion as a single dose on D0.
Otros nombres:
  • hUC-MSCs
Experimental: Phase IIa, Medium-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Otros nombres:
  • hUC-MSCs
Experimental: Phase IIa, High-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Otros nombres:
  • hUC-MSCs
Comparador de placebos: Phase IIa, Placebo Cohort
Multiple Electrolytes Injection
3 infusions in total, dosing interval ≥7 days

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Phase I : Incidence and number of subjects with treatment-emergent adverse events and serious adverse events.
Periodo de tiempo: 48 weeks
In this Phase I stage, safety is the primary endpoint. Types, frequencies, severities and causal relationships of all adverse events (AEs) and serious adverse events (SAEs) occurring from the first administration of study drug to the end of safety follow-up (48 weeks), assessed in accordance with the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 6.0; together with the proportion of adverse events judged by the investigator to be related to the study drug.
48 weeks
Phase II :FSH
Periodo de tiempo: at Week 24 post-treatment
To evaluate the changes from baseline in serum follicle-stimulating hormone (FSH) levels at Week 24 post-treatment.
at Week 24 post-treatment
Phase II :E2
Periodo de tiempo: at Week 24 post-treatment
To evaluate the changes from baseline in serum festradiol (E2) levels at Week 24 post-treatment.
at Week 24 post-treatment
Phase II :AMH
Periodo de tiempo: at Week 24 post-treatment
To evaluate the changes from baseline in serum anti-Müllerian hormone (AMH) levels at Week 24 post-treatment.
at Week 24 post-treatment

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Phase I: FSH
Periodo de tiempo: 48 weeks
To evaluate the changes from baseline in serum follicle-stimulating hormone (FSH) levels.
48 weeks
Phase I :E2
Periodo de tiempo: 48 weeks
To evaluate the changes from baseline in serum estradiol (E2) levels
48 weeks
Phase I : AMH
Periodo de tiempo: 48 weeks
To evaluate the changes from baseline in serum anti-Müllerian hormone (AMH) levels.
48 weeks
Phase II: Incidence and number of subjects with treatment-emergent adverse events and serious adverse events.
Periodo de tiempo: 48 weeks
In this Phase II stage, safety is the secondary endpoint. Types, frequencies, severities and causal relationships of all adverse events (AEs) and serious adverse events (SAEs) occurring from the first administration of study drug to the end of safety follow-up (48 weeks), assessed in accordance with the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 6.0; together with the proportion of adverse events judged by the investigator to be related to the study drug.
48 weeks
Phase I/II: AFC
Periodo de tiempo: 48 weeks
Changes from baseline in antral follicle count (AFC) by transvaginal ultrasound.
48 weeks
Phase I/II: endometrial thickness
Periodo de tiempo: 48 weeks
Changes from baseline in endometrial thickness measured by transvaginal ultrasound.
48 weeks
Phase I/II: menstrual recovery status
Periodo de tiempo: 48 weeks
Menstrual recovery status will be assessed via patient inquiry at each visit.
48 weeks
Phase I/II:Modified Kupperman Index
Periodo de tiempo: 48 weeks

To evaluate the changes in the Modified Kupperman Index from baseline across all post-baseline follow-up visits.

Modified Kupperman Index will be assessed through physician interview.The total score ranges from 0 to 63 points. Total score stratification: >30 points indicates severe symptoms, 16-30 points moderate symptoms, 6-15 points mild symptoms, and <6 points normal status.

48 weeks

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)

3 de agosto de 2026

Finalización primaria (Estimado)

30 de septiembre de 2028

Finalización del estudio (Estimado)

2 de agosto de 2029

Fechas de registro del estudio

Enviado por primera vez

27 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

19 de agosto de 2026

Publicado por primera vez (Actual)

20 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

20 de agosto de 2026

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

19 de agosto de 2026

Última verificación

1 de agosto 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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