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

19 agosto 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

59

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100730
        • Reclutamento
        • Peking Union Medical College Hospital
        • Contatto:
          • Qi Yu, Prof.
          • Numero di telefono: +86 10 6915 8621
          • Email: yuqimd@163.com

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Altri nomi:
  • hUC-MSCs
Sperimentale: 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.
Altri nomi:
  • hUC-MSCs
Sperimentale: 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.
Altri nomi:
  • hUC-MSCs
Sperimentale: Phase IIa, Medium-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Altri nomi:
  • hUC-MSCs
Sperimentale: Phase IIa, High-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Altri nomi:
  • hUC-MSCs
Comparatore placebo: Phase IIa, Placebo Cohort
Multiple Electrolytes Injection
3 infusions in total, dosing interval ≥7 days

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Phase I : Incidence and number of subjects with treatment-emergent adverse events and serious adverse events.
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Phase I: FSH
Lasso di tempo: 48 weeks
To evaluate the changes from baseline in serum follicle-stimulating hormone (FSH) levels.
48 weeks
Phase I :E2
Lasso di tempo: 48 weeks
To evaluate the changes from baseline in serum estradiol (E2) levels
48 weeks
Phase I : AMH
Lasso di tempo: 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.
Lasso di tempo: 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
Lasso di tempo: 48 weeks
Changes from baseline in antral follicle count (AFC) by transvaginal ultrasound.
48 weeks
Phase I/II: endometrial thickness
Lasso di tempo: 48 weeks
Changes from baseline in endometrial thickness measured by transvaginal ultrasound.
48 weeks
Phase I/II: menstrual recovery status
Lasso di tempo: 48 weeks
Menstrual recovery status will be assessed via patient inquiry at each visit.
48 weeks
Phase I/II:Modified Kupperman Index
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

3 agosto 2026

Completamento primario (Stimato)

30 settembre 2028

Completamento dello studio (Stimato)

2 agosto 2029

Date di iscrizione allo studio

Primo inviato

27 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

19 agosto 2026

Primo Inserito (Effettivo)

20 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

20 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

19 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • WG108-POI-I/IIa

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .