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A Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure (POF)

Primary Purpose

Primary Ovarian Insufficiency, Premature Ovarian Failure, Infertility

Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
human amniotic epithelial cells (hAECs) transplantation
Sponsored by
International Peace Maternity and Child Health Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Ovarian Insufficiency focused on measuring primary ovarian insufficiency, premature ovarian failure, Infertility, human amniotic epithelial cells transplantation

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. ≥18 and<45 years old.
  2. Female patients with documented diagnosis of POF: <40 years old, at least 4 months of amenorrhea not due to pregnancy, two FSH levels above 40 IU/L, at least one month apart.
  3. Not in other trial within 3 months prior to the start of this trial.
  4. Willing to participate in this trial and to give informed consent/assent before any procedures are performed in this trial.

Exclusion Criteria:

  1. History of, or evidence of current malignancy within the past 5 years.
  2. Severe functional impairment of vital organs.
  3. Abnormal karyotype.
  4. Coagulation disorders.
  5. Severe pelvic adhesions.
  6. Uncontrolled acute or chronic gynecologic inflammation.
  7. Congenital adrenal cortical hyperplasia.
  8. Cushing's syndrome.
  9. Thyroid dysfunction.
  10. Pituitary adenoma.
  11. Pituitary amenorrhea or Hypothalamic amenorrhea.
  12. Thrombophlebitis, venous thrombosis or artery thrombosis.
  13. History of Oophorocystectomy.
  14. Currently pregnant or breast-feeding.
  15. Currently receiving other treatment that might affect the efficacy and safety of stem cells.
  16. History of severe drug allergy.
  17. Active infection detected by chest X-ray/CT.
  18. HIV, TPAb positive.
  19. Mental illness.
  20. Currently participating in any other clinical trial that uses interventional drugs or examinations.
  21. Patients that are deemed, by the investigator, inappropriate to participate in this trial.

Sites / Locations

  • The International Peace Maternity and Child Health Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

hAECs transplantation

Arm Description

To clarify the safety and effectiveness of human amniotic epithelial cells transplantation for the treatment of POF patients

Outcomes

Primary Outcome Measures

Safety and Tolerability assessed by Adverse Events
Proportion of patients with adverse events (AEs), serious adverse events (SAEs) and adverse events of special interest (AESI,such as acute allergic reaction, ectopic mass formation related to treatment)

Secondary Outcome Measures

Change from baseline in bilateral ovarian volume
The ovarian volume will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Change from baseline in number of antral follicles (AFC)
The number of antral follicles developing will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Change from baseline in Follicle-stimulating hormone (FSH) serum level
Serum FSH level will be tested on 30th and 150th days after transplantation.
Change from baseline in Luteinizing hormone (LH), Estradiol (E2), Testosterone (T), Prolactin (PRL) , Anti-müllerian hormone (AMH) serum level
Serum LH, E2, T, PRL, AMH level will be tested on 30th and 150th days after transplantation.
Menstruation resumption
Patients will monitor for resumption of menses within 150 days after transplantation. If the menstruation resumption rate is over 30%, the treatment will be considered effective.
Endometrial thickness
The endometrial thickness will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Bone mineral density (BMD) measurements
The BMD will be tested on 150th day after transplantation.
Achievement of pregnancy
Achievement of pregnancy by natural or assisted conception methods, such as in vitro fertilization (IVF). The outcomes of pregnancy include conception, miscarriage and delivery. If the pregnancy rate is over 30%, the treatment will be considered effective.

Full Information

First Posted
September 6, 2016
Last Updated
February 27, 2023
Sponsor
International Peace Maternity and Child Health Hospital
Collaborators
Shanghai iCELL Biotechnology Co., Ltd, Shanghai, China
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1. Study Identification

Unique Protocol Identification Number
NCT02912104
Brief Title
A Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure
Acronym
POF
Official Title
A Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
June 20, 2020 (Actual)
Primary Completion Date
January 5, 2022 (Actual)
Study Completion Date
January 5, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
International Peace Maternity and Child Health Hospital
Collaborators
Shanghai iCELL Biotechnology Co., Ltd, Shanghai, China

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This project will clarify the safety and effectiveness of human amniotic epithelial cells transplantation for the treatment of primary ovarian failure (POF) patients and provide a new therapeutic method for patients with infertility.
Detailed Description
POF is a defect characterized by the premature depletion of ovarian follicles. Patients with POF suffer from amenorrhea, infertility, low levels of estrogen, and high gonadotropin concentration before the age of 40. The early failure of ovarian function leads to lost fertility and increases risk of osteoporosis and cardiovascular disease, which has serious impact on the patient's physical, mental health and family stability. The etiology of POF is complex, and so far there has not been any effective treatment. Recent study showed that human amniotic epithelial cells (hAECs), also known as the birth waste, are newly discovered adult stem cells. The hAECs have the ability to repair nerve damage, myocardial injury, as well as liver damage. hAECs have low immunogenicity and no ethical restrictions. Therefore, hAECs are expected to become the new seed cells for regenerative medicine. Our previous study was the first to show that human amniotic epithelial cells have the ability to restore folliculogenesis in a mouse model with chemotherapy-induced premature ovarian failure. Our further studies demonstrated that hAECs either directly transdifferentiated into granulosa cells, or inhibited tumor necrosis factor-alpha-mediated granulosa cell apoptosis and reduced the inflammatory reaction in ovaries induced by chemotherapeutics, regulating VEGFA and its receptors to induce follicular growth related to paracrine activity. Therefore, it is necessary to start the clinical study of human amniotic epithelial cells transplantation in the POF disease which may offer a novel therapeutic strategy for improving the quality of life of POF patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Ovarian Insufficiency, Premature Ovarian Failure, Infertility
Keywords
primary ovarian insufficiency, premature ovarian failure, Infertility, human amniotic epithelial cells transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
hAECs transplantation
Arm Type
Experimental
Arm Description
To clarify the safety and effectiveness of human amniotic epithelial cells transplantation for the treatment of POF patients
Intervention Type
Biological
Intervention Name(s)
human amniotic epithelial cells (hAECs) transplantation
Other Intervention Name(s)
hAECs transplantation
Intervention Description
hAECs are prepared and cultured using GMP(Good Manufacturing Practice, GMP) rules, 3×10^7 hAECs in 4.5ml is separately injected into ovarian tissue by bilateral ovarian artery infusion.
Primary Outcome Measure Information:
Title
Safety and Tolerability assessed by Adverse Events
Description
Proportion of patients with adverse events (AEs), serious adverse events (SAEs) and adverse events of special interest (AESI,such as acute allergic reaction, ectopic mass formation related to treatment)
Time Frame
150 days
Secondary Outcome Measure Information:
Title
Change from baseline in bilateral ovarian volume
Description
The ovarian volume will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Time Frame
150 days
Title
Change from baseline in number of antral follicles (AFC)
Description
The number of antral follicles developing will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Time Frame
150 days
Title
Change from baseline in Follicle-stimulating hormone (FSH) serum level
Description
Serum FSH level will be tested on 30th and 150th days after transplantation.
Time Frame
150 days
Title
Change from baseline in Luteinizing hormone (LH), Estradiol (E2), Testosterone (T), Prolactin (PRL) , Anti-müllerian hormone (AMH) serum level
Description
Serum LH, E2, T, PRL, AMH level will be tested on 30th and 150th days after transplantation.
Time Frame
150 days
Title
Menstruation resumption
Description
Patients will monitor for resumption of menses within 150 days after transplantation. If the menstruation resumption rate is over 30%, the treatment will be considered effective.
Time Frame
150 days
Title
Endometrial thickness
Description
The endometrial thickness will be assessed by pelvic ultrasound on 30th, 90th, 150th days after transplantation.
Time Frame
150 days
Title
Bone mineral density (BMD) measurements
Description
The BMD will be tested on 150th day after transplantation.
Time Frame
150 days
Title
Achievement of pregnancy
Description
Achievement of pregnancy by natural or assisted conception methods, such as in vitro fertilization (IVF). The outcomes of pregnancy include conception, miscarriage and delivery. If the pregnancy rate is over 30%, the treatment will be considered effective.
Time Frame
12 Months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥18 and<45 years old. Female patients with documented diagnosis of POF: <40 years old, at least 4 months of amenorrhea not due to pregnancy, two FSH levels above 40 IU/L, at least one month apart. Not in other trial within 3 months prior to the start of this trial. Willing to participate in this trial and to give informed consent/assent before any procedures are performed in this trial. Exclusion Criteria: History of, or evidence of current malignancy within the past 5 years. Severe functional impairment of vital organs. Abnormal karyotype. Coagulation disorders. Severe pelvic adhesions. Uncontrolled acute or chronic gynecologic inflammation. Congenital adrenal cortical hyperplasia. Cushing's syndrome. Thyroid dysfunction. Pituitary adenoma. Pituitary amenorrhea or Hypothalamic amenorrhea. Thrombophlebitis, venous thrombosis or artery thrombosis. History of Oophorocystectomy. Currently pregnant or breast-feeding. Currently receiving other treatment that might affect the efficacy and safety of stem cells. History of severe drug allergy. Active infection detected by chest X-ray/CT. HIV, TPAb positive. Mental illness. Currently participating in any other clinical trial that uses interventional drugs or examinations. Patients that are deemed, by the investigator, inappropriate to participate in this trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dongmei Lai, M.D.
Organizational Affiliation
The center of Laboratory, The international peace Maternity and child health Hospital,School of Medicine, Shanghai Jiaotong University, Shanghai,China,200030
Official's Role
Principal Investigator
Facility Information:
Facility Name
The International Peace Maternity and Child Health Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The public can require the data and protocol from clinicaltrials.gov posted by investigator
IPD Sharing Time Frame
2 years
IPD Sharing Access Criteria
public
IPD Sharing URL
https://clinicaltrials.gov
Citations:
PubMed Identifier
24406076
Citation
Wang F, Wang L, Yao X, Lai D, Guo L. Human amniotic epithelial cells can differentiate into granulosa cells and restore folliculogenesis in a mouse model of chemotherapy-induced premature ovarian failure. Stem Cell Res Ther. 2013 Oct 14;4(5):124. doi: 10.1186/scrt335.
Results Reference
result
PubMed Identifier
26303743
Citation
Zhang Q, Xu M, Yao X, Li T, Wang Q, Lai D. Human amniotic epithelial cells inhibit granulosa cell apoptosis induced by chemotherapy and restore the fertility. Stem Cell Res Ther. 2015 Aug 25;6(1):152. doi: 10.1186/s13287-015-0148-4.
Results Reference
result
PubMed Identifier
26664408
Citation
Yao X, Guo Y, Wang Q, Xu M, Zhang Q, Li T, Lai D. The Paracrine Effect of Transplanted Human Amniotic Epithelial Cells on Ovarian Function Improvement in a Mouse Model of Chemotherapy-Induced Primary Ovarian Insufficiency. Stem Cells Int. 2016;2016:4148923. doi: 10.1155/2016/4148923. Epub 2015 Nov 9.
Results Reference
result

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A Therapeutic Trial of Human Amniotic Epithelial Cells Transplantation for Primary Ovarian Failure

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