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

19 sierpnia 2026 zaktualizowane przez: 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.

Przegląd badań

Szczegółowy opis

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.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

59

Faza

  • Faza 2
  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chiny, 100730
        • Rekrutacyjny
        • Peking Union Medical College Hospital
        • Kontakt:
          • Qi Yu, Prof.
          • Numer telefonu: +86 10 6915 8621
          • E-mail: yuqimd@163.com

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Nie

Opis

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 studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Poczwórny

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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.
Inne nazwy:
  • hUC-MSCs
Eksperymentalny: 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.
Inne nazwy:
  • hUC-MSCs
Eksperymentalny: 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.
Inne nazwy:
  • hUC-MSCs
Eksperymentalny: Phase IIa, Medium-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Inne nazwy:
  • hUC-MSCs
Eksperymentalny: Phase IIa, High-Dose Cohort
Human Umbilical Cord Mesenchymal Stem Cells Injection
hUC-MSCs Injection, 3 infusions in total, dosing interval ≥7 days.
Inne nazwy:
  • hUC-MSCs
Komparator placebo: Phase IIa, Placebo Cohort
Multiple Electrolytes Injection
3 infusions in total, dosing interval ≥7 days

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Phase I : Incidence and number of subjects with treatment-emergent adverse events and serious adverse events.
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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

Miary wyników drugorzędnych

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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

3 sierpnia 2026

Zakończenie podstawowe (Szacowany)

30 września 2028

Ukończenie studiów (Szacowany)

2 sierpnia 2029

Daty rejestracji na studia

Pierwszy przesłany

27 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

19 sierpnia 2026

Pierwszy wysłany (Rzeczywisty)

20 sierpnia 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

20 sierpnia 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

19 sierpnia 2026

Ostatnia weryfikacja

1 sierpnia 2026

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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