Clinical Study of Recombinant Human Follitropin for Injection Assisted in COH Assisted IVF-ET
Primary Purpose
Ovarian Hyperstimulation Syndrome
Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Triptorelin for Injection
Recombinant Human Choriogonadotropin alfa Solution for Injection
Progesterone Soft Capsules
Sponsored by
About this trial
This is an interventional treatment trial for Ovarian Hyperstimulation Syndrome
Eligibility Criteria
Inclusion Criteria:
- Age is more than 20 years old and less than 39 years old, married.
- Applicable for ART controlled ovarian hyperstimulation, such as IVF/ET, ICSI, GIFT, ZIFT and so on.
- Regular menstrual cycle (25-35 days).
- 18kg/m2≤BMI<30kg/m2.
- The level of basic serum FSH <10IU / L in the 2nd-5th days of the menstrual cycle, the luteinizing hormone, estradiol and progesterone levels were normal.
- The screening period or recent three months of vaginal ultrasound examination showed that the shape of bilateral ovarian and uterine size were normal and 5 ≤ number of basal antral follicle in unilateral ovarian <10, and follicular diameter <10 mm.
- The in vitro fertilization and embryo transfer (IVF/ET) and (or) intracytoplasmic sperm injection (ICSI) technology were less than three times used prior to the reproductive treatment (provide copies of previous cases).
- Volunteer to participate and sign informed consent.
Exclusion Criteria:
- There are high risk of ovarian hyperstimulation syndrome (OHSS), such as the subject who has high response to gonadotropin in the previous ovarian hyperstimulation cycle, polycystic ovary syndrome (PCOS), the subject who has severe OHSS cancellation cycle.
- Affect the outcome of pregnancy-related diseases (any one): untreated hydrosalpinx, untreated uterine polyps, untreated uterine infection, stage Ⅲ ~ IV endometriosis, ovarian cyst> 4cm , uterine fibroids diameter> 4cm, pelvic benign tumor> 4cm, pituitary tumors and malignant tumors of tissues and organs.
- The subject has abnormal uterine bleeding.
- Affect pregnancy-related endocrine and metabolic diseases (any one): hyperprolactinemia, thyroid disease (including hyperthyroidism, hypothyroidism), hyperandrogenism, adrenal dysfunction (including adrenal hyperfunction, adrenal cortical dysfunction).
- The subject has severe liver and kidney dysfunction, which the levels of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are 2.5 times higher than the upper limit of normal value, and serum creatinine (Cr) and urea nitrogen (BUN) are 2 times higher than the upper limit of normal value.
- Severe heart disease, unstable angina pectoris, heart failure grade Ⅲ above, acute myocardial infarction and/or old myocardial infarction, hypertension diagnosed according to the 2010 edition of the Chinese Hypertension Prevention Guidelines.
- The subject who have contraindications or allergic history for gonadotropin-releasing hormone agonists (GnRH-a), rFSH/human menopausal gonadotropin (hMG), human chorionic gonadotropin (hCG), progesterone drugs.
- Positive HIV or syphilis.
- The subject has alcoholism, smoking, drug abuse, bad drug abuse habits.
- At least one of the spouses has received sperm donor or egg donor or PGD (genetic diagnosis before embryo transfer) and PGS (Preimplantation of embryos before genetic screening)。
- The subject received clomiphene or gonadotropin therapy within 1 month before screening。
- The subject was participated in last three months or are participating in other clinical research。
- Patients with positive serum pregnancy test.
- The investigators considered the subject inappropriate to be enrolled in this study.
Sites / Locations
- The first Affiliated Hospital of Anhui Medical University
- Sun Yat-sen Memorial Hospital
- The Sixth Affiliated Hospital of Sun Yat-sen University
- Xiangya Hospital Central South University
- Women's Hospital School of Medicine Zhejiang University
- Peking University Third Hospital
- Jiangsu Province Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Recombinant Human Follitropin
Gonal-F
Arm Description
Experimental group (domestic rhFSH, powder for injection, 5.5μg (75IU)/vial, initial dose 150-225IU/d, subcutaneous injection, adjust the dose according to ovarian reactivity after 5-7 days of injections, once a day until the HCG trigger day.
Positive control group (imported rhFSH, powder for injection, 5.5μg (75IU)/vial, initial dose 150-225IU/d, subcutaneous injection, adjust the dose according to ovarian reactivity after 5-7 days of injections, once a day until the HCG trigger day.
Outcomes
Primary Outcome Measures
The total number of oocytes obtained during the start-up period
Routine ova harvest to determine the number of obtained oocytes
Secondary Outcome Measures
The number of follicle-1
The number of follicle with diameter more than 18mm
The number of follicle-2
The number of follicle with diameter more than 18mm
Number of 2PN oocytes
Number of metaphase II oocytes
Number of transferred embryos
Number of high quality embryos
Fresh cycle embryo implantation
rhFSH administered days and vials; administered total dose of rhFSH (IU)
Serum E2 level
High quality embryos rate
Fertilization rate
Fresh cycle embryo implantation rate
Biochemical pregnancy rate
Clinical pregnancy rate
Continuous pregnancy rate
The number of follicle-3
The number of follicle with diameter between 14mm and 18mm.
The number of follicle-4
The number of follicle with diameter less than 14mm
Endometrium thickness (mm)
Full Information
NCT ID
NCT03071172
First Posted
February 20, 2017
Last Updated
February 28, 2017
Sponsor
Changchun GeneScience Pharmaceutical Co., Ltd.
Collaborators
Peking University Third Hospital, The First Affiliated Hospital with Nanjing Medical University, Women's Hospital School Of Medicine Zhejiang University, Xiangya Hospital of Central South University, Sixth Affiliated Hospital, Sun Yat-sen University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, The First Affiliated Hospital of Anhui Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03071172
Brief Title
Clinical Study of Recombinant Human Follitropin for Injection Assisted in COH Assisted IVF-ET
Official Title
Clinical Study of Recombinant Human Follitropin for Injection Assisted in Controlled Ovarian Hyperstimulation Assisted IVF-ET
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2017 (Anticipated)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
May 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Changchun GeneScience Pharmaceutical Co., Ltd.
Collaborators
Peking University Third Hospital, The First Affiliated Hospital with Nanjing Medical University, Women's Hospital School Of Medicine Zhejiang University, Xiangya Hospital of Central South University, Sixth Affiliated Hospital, Sun Yat-sen University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, The First Affiliated Hospital of Anhui Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study was to evaluate the efficacy and safety of domestic recombinant human follicle stimulating hormone (rhFSH) stimulating ovarian to promote follicular development before assisted reproductive technology, which was non-inferiority than that of the imported rhFSH.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Hyperstimulation Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
252 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Recombinant Human Follitropin
Arm Type
Experimental
Arm Description
Experimental group (domestic rhFSH, powder for injection, 5.5μg (75IU)/vial, initial dose 150-225IU/d, subcutaneous injection, adjust the dose according to ovarian reactivity after 5-7 days of injections, once a day until the HCG trigger day.
Arm Title
Gonal-F
Arm Type
Active Comparator
Arm Description
Positive control group (imported rhFSH, powder for injection, 5.5μg (75IU)/vial, initial dose 150-225IU/d, subcutaneous injection, adjust the dose according to ovarian reactivity after 5-7 days of injections, once a day until the HCG trigger day.
Intervention Type
Drug
Intervention Name(s)
Triptorelin for Injection
Other Intervention Name(s)
Gonadotropin releasing hormone agonists
Intervention Description
Drugs for IVF-ET (in vitro fertilization and embryo transfer).
Intervention Type
Drug
Intervention Name(s)
Recombinant Human Choriogonadotropin alfa Solution for Injection
Intervention Description
Drugs for IVF-ET (in vitro fertilization and embryo transfer).
Intervention Type
Drug
Intervention Name(s)
Progesterone Soft Capsules
Intervention Description
Drugs for IVF-ET (in vitro fertilization and embryo transfer).
Primary Outcome Measure Information:
Title
The total number of oocytes obtained during the start-up period
Description
Routine ova harvest to determine the number of obtained oocytes
Time Frame
On the days of ovum picking up (hCG trigger 36-38h)
Secondary Outcome Measure Information:
Title
The number of follicle-1
Description
The number of follicle with diameter more than 18mm
Time Frame
on the day of hCG day
Title
The number of follicle-2
Description
The number of follicle with diameter more than 18mm
Time Frame
on the fifth day of rhFSH ovarian stimulation
Title
Number of 2PN oocytes
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
Number of metaphase II oocytes
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up, which only collected during ICSI cycle.
Title
Number of transferred embryos
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
Number of high quality embryos
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
Fresh cycle embryo implantation
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
rhFSH administered days and vials; administered total dose of rhFSH (IU)
Time Frame
Collected on the day of hCG day.
Title
Serum E2 level
Time Frame
Collected on the day of hCG day.
Title
High quality embryos rate
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
Fertilization rate
Time Frame
Collected on the day of embryo transfer day after three days of ovum picking up.
Title
Fresh cycle embryo implantation rate
Time Frame
Collected between 28-35 days after embryo transfer.
Title
Biochemical pregnancy rate
Time Frame
Collected between 14-16 days after embryo transfer.
Title
Clinical pregnancy rate
Time Frame
Collected between 28-35 days after embryo transfer.
Title
Continuous pregnancy rate
Time Frame
Collected after 12 weeks of embryo transfer.
Title
The number of follicle-3
Description
The number of follicle with diameter between 14mm and 18mm.
Time Frame
on the day of hCG day
Title
The number of follicle-4
Description
The number of follicle with diameter less than 14mm
Time Frame
on the day of hCG day
Title
Endometrium thickness (mm)
Time Frame
on the day of hCG
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
39 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age is more than 20 years old and less than 39 years old, married.
Applicable for ART controlled ovarian hyperstimulation, such as IVF/ET, ICSI, GIFT, ZIFT and so on.
Regular menstrual cycle (25-35 days).
18kg/m2≤BMI<30kg/m2.
The level of basic serum FSH <10IU / L in the 2nd-5th days of the menstrual cycle, the luteinizing hormone, estradiol and progesterone levels were normal.
The screening period or recent three months of vaginal ultrasound examination showed that the shape of bilateral ovarian and uterine size were normal and 5 ≤ number of basal antral follicle in unilateral ovarian <10, and follicular diameter <10 mm.
The in vitro fertilization and embryo transfer (IVF/ET) and (or) intracytoplasmic sperm injection (ICSI) technology were less than three times used prior to the reproductive treatment (provide copies of previous cases).
Volunteer to participate and sign informed consent.
Exclusion Criteria:
There are high risk of ovarian hyperstimulation syndrome (OHSS), such as the subject who has high response to gonadotropin in the previous ovarian hyperstimulation cycle, polycystic ovary syndrome (PCOS), the subject who has severe OHSS cancellation cycle.
Affect the outcome of pregnancy-related diseases (any one): untreated hydrosalpinx, untreated uterine polyps, untreated uterine infection, stage Ⅲ ~ IV endometriosis, ovarian cyst> 4cm , uterine fibroids diameter> 4cm, pelvic benign tumor> 4cm, pituitary tumors and malignant tumors of tissues and organs.
The subject has abnormal uterine bleeding.
Affect pregnancy-related endocrine and metabolic diseases (any one): hyperprolactinemia, thyroid disease (including hyperthyroidism, hypothyroidism), hyperandrogenism, adrenal dysfunction (including adrenal hyperfunction, adrenal cortical dysfunction).
The subject has severe liver and kidney dysfunction, which the levels of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are 2.5 times higher than the upper limit of normal value, and serum creatinine (Cr) and urea nitrogen (BUN) are 2 times higher than the upper limit of normal value.
Severe heart disease, unstable angina pectoris, heart failure grade Ⅲ above, acute myocardial infarction and/or old myocardial infarction, hypertension diagnosed according to the 2010 edition of the Chinese Hypertension Prevention Guidelines.
The subject who have contraindications or allergic history for gonadotropin-releasing hormone agonists (GnRH-a), rFSH/human menopausal gonadotropin (hMG), human chorionic gonadotropin (hCG), progesterone drugs.
Positive HIV or syphilis.
The subject has alcoholism, smoking, drug abuse, bad drug abuse habits.
At least one of the spouses has received sperm donor or egg donor or PGD (genetic diagnosis before embryo transfer) and PGS (Preimplantation of embryos before genetic screening)。
The subject received clomiphene or gonadotropin therapy within 1 month before screening。
The subject was participated in last three months or are participating in other clinical research。
Patients with positive serum pregnancy test.
The investigators considered the subject inappropriate to be enrolled in this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rui Yang
Phone
010-82265080
Email
yrjeff@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rong Li, Doctor
Organizational Affiliation
Peking University Third Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The first Affiliated Hospital of Anhui Medical University
City
Hefei
State/Province
Anhui
Country
China
Facility Name
Sun Yat-sen Memorial Hospital
City
Guangzhou
State/Province
Guangdong
Country
China
Facility Name
The Sixth Affiliated Hospital of Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
Country
China
Facility Name
Xiangya Hospital Central South University
City
Changsha
State/Province
Hunan
Country
China
Facility Name
Women's Hospital School of Medicine Zhejiang University
City
Hangzhou
State/Province
Zhejiang
Country
China
Facility Name
Peking University Third Hospital
City
Beijing
Country
China
Facility Name
Jiangsu Province Hospital
City
Nanjing
Country
China
12. IPD Sharing Statement
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Clinical Study of Recombinant Human Follitropin for Injection Assisted in COH Assisted IVF-ET
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