Back to resultsAn Efficacy and Safety Study of Corifollitropin Alfa (MK-8962) in Contrast to Recombinant FSH for Use in Controlled Ovarian Stimulation of Indian Women (P07056, Also Known as MK-8962-029)
Primary Purpose
Infertility
Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
MK-8962
recFSH
Ganirelix
human Chorionic Gonadotropin (hCG)
Progesterone
Sponsored by
About this trial
This is an interventional treatment trial for Infertility
Eligibility Criteria
Inclusion Criteria:
Please Note: In this trial an Indian female participant is defined as a woman 1) with native Indian parents, and 2) who is also in possession of an Indian identification card.
- Indian woman with an indication for COS and IVF/ICSI, but has not yet undergone IVF/ICSI.
- Body mass index (BMI) of 18.0 to 32.0 kg/m2
- Regular spontaneous menstrual cycle (ie, a menstrual schedule that consistently occurs within a range of 24 to 35 days)
- Access to available ejaculatory sperm. Use of donated and/or cryopreserved sperm is allowed, however sperm obtained via surgical sperm retrieval is not allowed.
- Results documented as 'within normal limits' from clinical laboratory tests (ie, complete blood count [CBC], blood chemistries, and urinalysis).
- Normal cervical smear result obtained within 12 months prior to study enrollment, otherwise test will be performed during screening.
- Able to adhere to dose and study visit schedules
Exclusion Criteria:
- Has a recent (ie, within 3 years prior to enrollment in study) history of/or
any active endocrine abnormality, treated or untreated.
- Contraindicated use of gonadotropins
- History of ovarian hyper-responsiveness
- History of/or current polycystic ovary syndrome (PCOS)
- Has less than 2 ovaries or has any other ovarian abnormality, including endometrioma (greater than 10 mm in size), and/or has unilateral or bilateral hydrosalpinx and/or intrauterine fibroids (5 cm in size or greater), confirmed by an ultrasound scan.
- Has any clinically relevant pathology that may impair embryo implantation or continuation of pregnancy.
- Experienced more than three unsuccessful COS cycles for IVF/ICSI since
the last established ongoing pregnancy, if applicable.
- History of non- or low ovarian response to FSH and/or Menopausal Gonadotropin (hMG) treatment.
- History of recurrent miscarriage (ie, 3 or more)
- Positive test results for Human Immunodeficiency Virus (HIV) or
Hepatitis B
- Recent history of/or current epilepsy, thrombophilia, diabetes, cardiovascular, gastro-intestinal, hepatic, renal or pulmonary or auto-immune disease, any of which required or requires treatment.
- Smokes or recently stopped smoking (ie, within 3 months of study enrollment)
- History of/or active alcohol and/or drug abuse (ie, within 12 months prior to study enrollment).
- Previous use of corifollitropin alfa
- Use of hormonal agents known to affect ovulation or any drug/agent considered to be teratogenic
- Use of any experimental drug within 3 months prior to study enrollment or participation in another clinical study, other than one that is survey-questionnaire based.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Single-Dose MK-8962 + recFSH
Reference Group recFSH only
Arm Description
Outcomes
Primary Outcome Measures
Number of Cumulus-Oocyte-Complexes Retrieved During Oocyte Pick-up
The criterion of hCG administration is defined as three or more follicles ≥17 mm, confirmed by ultrasound. Oocyte pick up occurs 34-36 hours after the Day of hCG Administration, based on confirmed ultrasound findings.
Secondary Outcome Measures
Confirmation of Vital Pregnancy
Per study protocol, vital pregnancy is defined as the presence of at least one fetus with heart activity at approximately 5 weeks (ie, ~ 35 days) after Day of Embryo Transfer in the COS treatment cycle.
Percentage of Participants with Moderate or Severe Ovarian Hyperstimulation Syndrome (OHSS)
Per study protocol, OHSS is defined as more than 30 follicles ≥11 mm in size demonstrated by ultrasound.
Number of Participants with an Ongoing Pregnancy
Per study protocol, ongoing pregnancy is defined as confirmed pregnancy at 10 or more weeks ( ~ 70 days) after Day of Embryo Transfer, documented by a positive pregnancy test and ultrasound scan demonstrating at least one gestational sac with heart activity.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01599494
Brief Title
An Efficacy and Safety Study of Corifollitropin Alfa (MK-8962) in Contrast to Recombinant FSH for Use in Controlled Ovarian Stimulation of Indian Women (P07056, Also Known as MK-8962-029)
Official Title
A Multi-center, Open-label, Randomized Trial in India to Investigate the Efficacy and Safety of a Single Injection of MK-8962 (Corifollitropin Alfa) to Induce Multifollicular Development for Controlled Ovarian Stimulation Using Daily Recombinant FSH as a Reference (Phase III, Protocol No. MK-8962-029-00 [Also Known as SCH900962, P07056])
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Withdrawn
Study Start Date
March 2014 (undefined)
Primary Completion Date
May 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Organon and Co
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study, conducted in India, will be recruiting women participants who are between the ages of 18 and 42, and who have an indication for controlled ovarian stimulation (COS), but have not yet undergone in-vitro fertilization and/or intracytoplasmic sperm injection (IVF/ICSI). The study is designed to compare the difference in oocyte (immature egg cell) production after administration of the investigative drug, MK-8962 (corifollitropin alfa) + recombinant follicle stimulating hormone (recFSH), in contrast to use of only the reference drug, recFSH.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single-Dose MK-8962 + recFSH
Arm Type
Experimental
Arm Title
Reference Group recFSH only
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
MK-8962
Other Intervention Name(s)
Corifollitropin alfa
Intervention Description
MK-8962 is supplied in a ready-to-use prefilled syringe containing
100 microgram (μg) or 150 μg corifollitropin alfa per 0.5 mL. Participants are randomized to receive a single subcutaneous (SC) injection of MK-8962 in the abdominal wall on Cycle Day 2 or Cycle Day 3. Dose of administered MK-8962 is weight-based. Participants who weigh 60 kilograms (kg) or less will be given 100 μg MK-8962 and those who weigh more than 60 kg will be given 150 μg MK-8962.
Intervention Type
Drug
Intervention Name(s)
recFSH
Other Intervention Name(s)
follitropin beta
Intervention Description
Recombinant Follicle Stimulating Hormone (recFSH) will be supplied as a ready-to-use solution in a 600 IU cartridge for SC injection via the recFSH Pen. Starting on Day 2 or 3 of the menstrual cycle (Stimulation Day 1), recFSH will be administered daily, each morning, via injections in the abdominal wall. A starting dose of between 150 - 300 IU will be administered and is fixed for the first week of stimulation. After 6 days, and based on each participant's individual response, the Investigator may decide to reduce the fixed dose for the remainder of the study. The maximum duration of stimulation is 19 days; recFSH will not be administered on the Day of hCG Administration.
Intervention Type
Drug
Intervention Name(s)
Ganirelix
Other Intervention Name(s)
Ganirelix acetate or Ganirelix diacetate
Intervention Description
0.25 mg/day SC injection in the upper leg, administered on Stimulation Day 5 up to and including Day of hCG Administration
Intervention Type
Drug
Intervention Name(s)
human Chorionic Gonadotropin (hCG)
Other Intervention Name(s)
human Chorionic Gonadotrophin
Intervention Description
Single dose of 10,000 or 5,000 IU hCG, administered via SC injection on Day of hCG Administration.
Intervention Type
Drug
Intervention Name(s)
Progesterone
Other Intervention Name(s)
Crinone®
Intervention Description
Crinone 8% (90 mg) gel administered intravaginally via a single-use, one piece polyethylene vaginal applicator once-daily on Day of Oocyte Pick-up or 1 day later and continued for at least 6 weeks or either up to menses or up to a negative pregnancy test performed at least 18 days after Day of Oocyte Pick-up.
Primary Outcome Measure Information:
Title
Number of Cumulus-Oocyte-Complexes Retrieved During Oocyte Pick-up
Description
The criterion of hCG administration is defined as three or more follicles ≥17 mm, confirmed by ultrasound. Oocyte pick up occurs 34-36 hours after the Day of hCG Administration, based on confirmed ultrasound findings.
Time Frame
34 to 36 hours after Day of Administration of Human Chorionic Gonadotropin (hCG)
Secondary Outcome Measure Information:
Title
Confirmation of Vital Pregnancy
Description
Per study protocol, vital pregnancy is defined as the presence of at least one fetus with heart activity at approximately 5 weeks (ie, ~ 35 days) after Day of Embryo Transfer in the COS treatment cycle.
Time Frame
Post treatment; at 35 days from Day of Embryo Transfer
Title
Percentage of Participants with Moderate or Severe Ovarian Hyperstimulation Syndrome (OHSS)
Description
Per study protocol, OHSS is defined as more than 30 follicles ≥11 mm in size demonstrated by ultrasound.
Time Frame
From Baseline up to 10 weeks after Day of Embryo Transfer
Title
Number of Participants with an Ongoing Pregnancy
Description
Per study protocol, ongoing pregnancy is defined as confirmed pregnancy at 10 or more weeks ( ~ 70 days) after Day of Embryo Transfer, documented by a positive pregnancy test and ultrasound scan demonstrating at least one gestational sac with heart activity.
Time Frame
Post treatment; at approximately 10 weeks from Day of Embryo Transfer
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Please Note: In this trial an Indian female participant is defined as a woman 1) with native Indian parents, and 2) who is also in possession of an Indian identification card.
Indian woman with an indication for COS and IVF/ICSI, but has not yet undergone IVF/ICSI.
Body mass index (BMI) of 18.0 to 32.0 kg/m2
Regular spontaneous menstrual cycle (ie, a menstrual schedule that consistently occurs within a range of 24 to 35 days)
Access to available ejaculatory sperm. Use of donated and/or cryopreserved sperm is allowed, however sperm obtained via surgical sperm retrieval is not allowed.
Results documented as 'within normal limits' from clinical laboratory tests (ie, complete blood count [CBC], blood chemistries, and urinalysis).
Normal cervical smear result obtained within 12 months prior to study enrollment, otherwise test will be performed during screening.
Able to adhere to dose and study visit schedules
Exclusion Criteria:
- Has a recent (ie, within 3 years prior to enrollment in study) history of/or
any active endocrine abnormality, treated or untreated.
Contraindicated use of gonadotropins
History of ovarian hyper-responsiveness
History of/or current polycystic ovary syndrome (PCOS)
Has less than 2 ovaries or has any other ovarian abnormality, including endometrioma (greater than 10 mm in size), and/or has unilateral or bilateral hydrosalpinx and/or intrauterine fibroids (5 cm in size or greater), confirmed by an ultrasound scan.
Has any clinically relevant pathology that may impair embryo implantation or continuation of pregnancy.
Experienced more than three unsuccessful COS cycles for IVF/ICSI since
the last established ongoing pregnancy, if applicable.
History of non- or low ovarian response to FSH and/or Menopausal Gonadotropin (hMG) treatment.
History of recurrent miscarriage (ie, 3 or more)
Positive test results for Human Immunodeficiency Virus (HIV) or
Hepatitis B
Recent history of/or current epilepsy, thrombophilia, diabetes, cardiovascular, gastro-intestinal, hepatic, renal or pulmonary or auto-immune disease, any of which required or requires treatment.
Smokes or recently stopped smoking (ie, within 3 months of study enrollment)
History of/or active alcohol and/or drug abuse (ie, within 12 months prior to study enrollment).
Previous use of corifollitropin alfa
Use of hormonal agents known to affect ovulation or any drug/agent considered to be teratogenic
Use of any experimental drug within 3 months prior to study enrollment or participation in another clinical study, other than one that is survey-questionnaire based.
12. IPD Sharing Statement
Learn more about this trial
An Efficacy and Safety Study of Corifollitropin Alfa (MK-8962) in Contrast to Recombinant FSH for Use in Controlled Ovarian Stimulation of Indian Women (P07056, Also Known as MK-8962-029)
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