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Efficacy Study of Granulocyte-macrophage Colony Stimulating Factor (GM-CSF) for Use in Human IVF

The Effect of Granulocyte-macrophage Colony Stimulating Factor (GM-CSF) During in Vitro Culture of Human Embryos on Subsequent Implantation Rates.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00565747
Acronym
GM-CSF
Enrollment
1332
Registered
2007-11-30
Start date
2007-11-30
Completion date
2011-09-30
Last updated
2015-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Keywords

GM-CSF, infertility

Brief summary

This study is to assess whether addition of 2 ng/ml GM-CSF into a specific culture medium will increase the chance of a pregnancy after in vitro fertilisation.

Detailed description

Throughout its development, the embryo is naturally exposed to a large number of cytokines and growth factors that are present in the woman's reproductive organs. A growing body of evidence indicates that these factors play a physiological role in the regulation of normal development of the pre-implanted embryo and that these factors therefore help to increase the implantation of the embryo and subsequently ensure optimal development of both foetus and placenta. The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) has been shown to be present in the female reproductive organs during early pregnancy in mice, sheep, cows and humans. 2 ng/ml GM-CSF has been proven safe in a previous study presented at the European Society of Human Reproduction and Embrylogy (ESHRE) congress 2007 (A. Loft et al. 2007). The present investigation (DK001) is to our knowledge the first large prospective randomised in vivo study in humans. Previous publications counting one Korean pilotstudy of 154 women prospectively randomised between culture medium with and without GM-CSF 2 ng/ml (Kim et al., 2001), showing a significant effect of GM-CSF on embryo implantation rate. Based on this knowledge we hypothesize that culture of human embryos in the presence of GM-CSF will significantly increase the implantation rate also in a larger population. This hypothesis is being tested by conducting a multicentre, randomised, parallel group, double-blind, placebo-controlled study with adaptive design, performed at 14 study centres. Each patient will participate in the study from retrieval of oocytes following standard hormonal treatment and until the 12th gestational week. Further a follow-up will be performed on pregnancies and children born. The test group will include a standard culture medium with 2 ng/ml GM-CSF added from the time of insemination, and the control group will be the exact same medium but without any additions. All procedures are according to standards of the clinic, with applied standard media except for the patient randomised study medium which is used for oocyte insemination, embryo culture and transfer. Embryo transfer will be performed Day 3. An interim analysis has been performed for final sample size calculation.

Interventions

DEVICETest culture

A standard culture medium with added GM-CSF (ready-to-use)

DEVICEControl culture

The same standard culture medium, but without any additions (ready-to-use)

Sponsors

Origio A/S
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* The couple or single woman has signed an informed consent form before any trial-related activities. * In Vitro Fertilization (IVF) or IntraCytoplasmic Sperm Injection (ICSI) treatment indicated * 25-39 years of age (both inclusive) * Regular menstrual cycle: 21-35 days (both inclusive) * Women treated with a standard Gonadotropin-Releasing Hormone (GnRH) agonist or antagonist protocol and a Follicle Stimulating Hormone (FSH) / human Menopausal Gonadotropin (hMG) starting dose between 100 and 300 IU daily. * human Chorionic Gonadotropin (hCG) administration when the leading follicle has a calculated diameter of minimum 17 mm, or the day after. * At least 3 follicles with a calculated diameter of ≥ 14 mm at the day of hCG.

Exclusion criteria

* The woman has previously participated in the DK001 study. * Use of assisted hatching. * Indication for Testicular Sperm Aspiration (TESA) or Percutaneous Epididymal Sperm Aspiration (PESA) * Any medical conditions or genetic disorders prohibiting IVF/ICSI or interfering with the interpretation of results of the study (including pre-implantation genetic diagnostics). * Use of any investigational drug within 30 days before oocyte retrieval * Any severe chronic disease of relevance for reproductive function. * Oocyte donation patients (donor or recipient).

Design outcomes

Primary

MeasureTime frameDescription
Ongoing Implantation Rate Week 7Approximately 5 weeks from oocyte pick-up (corresponding to 7 weeks from ovulation)Defined as number of gestational sacs with fetal heart beat, shown by ultrasound in gestational week 7 in percentage of number of embryo transferred.

Secondary

MeasureTime frameDescription
Number of Top Quality Embryos (TQE´s)3 days from oocyte pick-upNumber of 4-5 cell embryo at 44 hours,at least 7 cell embryo at 68 hours, maximum 20% fragmentation, equally large blastomeres (less than 25% difference in size),No signs of multinucleation. Calculated in percentage of number of 2 pronuclei (2PN) oocytes.
Live BirthUntil 7 days after birthSubject having at least one live birth. Including a foetus which breathes or shows any other evidence of life after expulsion/extraction from its mother. The definition is independent of the duration of the pregnancy (ICMART/WHO criteria).

Countries

Denmark, Sweden

Participant flow

Recruitment details

Overall recruitment period: October 2007 until August 2010. Patients were recruited at both public and private IVF clinics

Pre-assignment details

Patients with informed consent but where it turned out that the inclusion/exclusion criteria were not fulfilled before assignment to groups, were excluded from the per-protocol (PP) analysis.

Participants by arm

ArmCount
Test Culture
Culture with 2 ng/ml GM-CSF
654
Control Culture
Culture without GM-CSF
678
Total1,332

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyNo embryo transfer6773

Baseline characteristics

CharacteristicControl CultureTotalTest Culture
Age, Continuous32.4 Years
STANDARD_DEVIATION 3.8
32.3 Years
STANDARD_DEVIATION 3.8
32.2 Years
STANDARD_DEVIATION 3.7
Region of Enrollment
Denmark
635 participants1245 participants610 participants
Region of Enrollment
Sweden
43 participants87 participants44 participants
Sex: Female, Male
Female
678 Participants1332 Participants654 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
6 / 6546 / 678
serious
Total, serious adverse events
13 / 6548 / 678

Outcome results

Primary

Ongoing Implantation Rate Week 7

Defined as number of gestational sacs with fetal heart beat, shown by ultrasound in gestational week 7 in percentage of number of embryo transferred.

Time frame: Approximately 5 weeks from oocyte pick-up (corresponding to 7 weeks from ovulation)

Population: PP-population

ArmMeasureValue (NUMBER)
Test CultureOngoing Implantation Rate Week 723.5 percentage of transferred embryos
Control CultureOngoing Implantation Rate Week 720.0 percentage of transferred embryos
Secondary

Live Birth

Subject having at least one live birth. Including a foetus which breathes or shows any other evidence of life after expulsion/extraction from its mother. The definition is independent of the duration of the pregnancy (ICMART/WHO criteria).

Time frame: Until 7 days after birth

Population: PP-population

ArmMeasureValue (NUMBER)
Test CultureLive Birth28.9 percentage of transfer patients
Control CultureLive Birth24.1 percentage of transfer patients
Secondary

Number of Top Quality Embryos (TQE´s)

Number of 4-5 cell embryo at 44 hours,at least 7 cell embryo at 68 hours, maximum 20% fragmentation, equally large blastomeres (less than 25% difference in size),No signs of multinucleation. Calculated in percentage of number of 2 pronuclei (2PN) oocytes.

Time frame: 3 days from oocyte pick-up

Population: PP-population

ArmMeasureValue (NUMBER)
Test CultureNumber of Top Quality Embryos (TQE´s)15.6 percentage of 2PN's
Control CultureNumber of Top Quality Embryos (TQE´s)16.8 percentage of 2PN's

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026