Efficacy of Recombinant Human G-CSF in Women With Unexplained Recurrent Miscarriage

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-44
SponsorFakih IVF Fertility Center

About this trial

Recurrent pregnancy loss (RPL), commonly referred to as recurrent miscarriage, affects approximately 1-2% of couples attempting to conceive. In nearly half of these cases, no definitive cause can be identified despite thorough clinical evaluation. A circumstance that is both distressing and disorienting for affected families, particularly in settings such as the United Arab Emirates (UAE), where childbearing carries significant personal and cultural weight.

One leading hypothesis is that the underlying problem may not lie with the embryo itself, but with the way the mother's immune system responds to a developing pregnancy. Under normal physiological conditions, the maternal body must establish immune tolerance toward an embryo that is genetically half-foreign in origin. In some women, this tolerance mechanism may be impaired, reducing the likelihood that a pregnancy will successfully implant and progress.

This study will evaluate whether granulocyte colony-stimulating factor (G-CSF) a naturally occurring substance that normally stimulates the production of immune cells can help address this issue by modulating an overactive immune response and enhancing the uterine environment's capacity to support pregnancy. Notably, the study will enroll only women whose embryos have undergone genetic testing and been confirmed to be chromosomally normal. This eliminates embryo quality as a contributing factor to pregnancy loss and allows for a clearer assessment of whether G-CSF itself influences outcomes.

Earlier small-scale studies, including preliminary work conducted at our own centre, have shown encouraging results. This new trial builds on that foundation by enrolling a larger cohort, comparing G-CSF against a placebo (an inactive comparison treatment), and evaluating a simpler route of administration; subcutaneous injection, rather than direct infusion into the uterus. Together, these design features aim to provide the most reliable evidence to date on whether this treatment can meaningfully help couples affected by unexplained recurrent pregnancy loss.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women aged 18-44 years

≥2 unexplained pregnancy losses

Undergoing IVF with PGT-A tested embryos

BMI 19-35 kg/m² 6.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Placebo control

    Drug

    Subcutaneous injection of Recombinant G-CSF daily from embryo transfer until 12 weeks' gestation

  • Recombinant G-CSF

    Drug

    Subcutaneous injection of Recombinant G-CSF daily from embryo transfer until 12 weeks' gestation

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Recombinant G-CSF 130 mcg SCExperimental treatment 1 intervention
Group B: Placebo Control: Placebo SCPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Clinical pregnancy rate

Clinical pregnancy confirmation by transvaginal ultrasound at 16 weeks' gestation.

Time frame
From enrollment to 16 weeks gestation

Secondary outcomes

1

Live birth rate

Time frame
From enrollment to approximately 40 weeks' gestation.
2

Ongoing Pregnancy Rate

16 - 34 weeks gestation by serial ultrasound.

Time frame
From 16 weeks to 34 weeks gestation.
3

Early Pregnancy Loss rate

Pregnancy loss confirmed by a transvaginal ultrasound.

Time frame
From FET (Fetal Embryo Transfer) to 12 weeks gestation
4

Rate of Adverse pregnancy outcomes (APOs)

Rate of Miscarriage, stillbirth, neonatal outcomes (birth weight, NICU admission, congenital anomalies) and maternal outcomes assessed using several methods including transvaginal ultrasound and clinical assessment.

Time frame
From enrollment to approximately 40 weeks gestation

Other outcomes

Sponsors and contacts

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