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CompletedNCT02349945Updated Jul 12, 2016

FSH Receptor Polymorphism p.N680S and Efficacy of FSH Therapy

A Phase 2/3 interventional study of follitropin alpha in Male Infertility, sponsored by Azienda USL Modena. Completed at 6 sites in 2 countries. Open to male participants aged 20 Years to 50 Years. Per ClinicalTrials.gov, last updated 2016-07-12.

Sponsored by Azienda USL Modena · Phase 2/3, Interventional, and Treatment

Phase
Phase 2/3
Study type
Interventional
Enrollment
88
Allocation
Non-randomized
Ages
20 Years to 50 Years
Sex
Male
01

Study summary

CONDITION: Idiopathic male infertility In men with idiopathic infertility, the sperm DNA fragmentation index (DFI) within 12 weeks of FSH therapy and 12 weeks follow-up improves depending on the FSHR genotype as assessed by the non-synonymous SNP rs6166 (wild type or p.N680S).

This is a phase II b, multicenter, prospective, open label, one arm, clinical trial stratified according to the patient's genotype.

INTERVENTION: FSH therapy (150 I.U. sc every other day for 12 weeks) in infertile men who are homozygous for the wild-type FSHR or the p.N680S allele of the FSHR. Duration of intervention per patient: 12 weeks

Primary efficacy endpoint: Sperm DFI. Number of patients with an improvement in DFI > 60% Key secondary endpoint(s): pregnancy, semen parameters, serum levels of inhibin B and AMH.

Read the detailed description

Male factor infertility is responsible for about 50% of cases of involuntary couple infertility and remains idiopathic in about half of the cases. At present, there are no consistently effective treatments for male idiopathic infertility. Since follicle-stimulating hormone (FSH) is fundamental for spermatogenesis, recombinant hFSH is empirically used for male infertility treatment. The response to FSH, however, is highly variable and while sperm parameters improve in some patients, about 50% of the subjects do not clearly respond to FSH. Several studies were performed in the past and a recent Cochrane meta-analysis showed that FSH treatment of male idiopathic infertility overall significantly improves pregnancy rate. Nevertheless, no predictive marker of response to FSH, allowing a stratified therapeutic approach, was identified so far.

The sperm DNA fragmentation index (DFI) provides an estimation of genetic integrity of spermatozoa and was shown to improve significantly after FSH treatment. Therefore, DFI could be used as a pharmacodynamic marker of FSH in the male.

In women, the response to FSH varies depending on the FSH receptor (FSHR) genotype, as determined by the non-synonymous SNP rs6166, which exchanges the amino acid Asn to Ser in codon 680. This SNP is very common, with a minor allele frequency of 0.4. Women homozygous for Ser at amino acid position 680 of the FSHR are less sensitive to endogenous and exogenous FSH compared to those homozygous for Asn and require more FSH for multiple follicular growth and maturation in assisted reproduction. The investigators hypothesize that the variable response to FSH in unselected infertile men is due to a different individual sensitivity to FSH as determined by the common FSHR polymorphism rs6166. In particular the investigators will test the hypothesis that men homozygous for Asn at 680 (wild type) will respond better to exogenous FSH treatment in terms of sperm DFI compared to men homozygous for Ser, assessing sperm DFI as pharmacodynamic parameter of FSH.

Men with idiopathic infertility and normal serum FSH levels, candidate for treatment with FSH, will be recruited. Men with a sperm DFI > 15% will be included in the trial if carriers of the homozygous Asn/Asn or Ser/Ser at aminoacid position 680. The FSHR genotype will be assessed centrally and the physician will only receive the information whether the patient is eligible for entering the trial (i.e. homozygous) but both the physician and the patient will remain blind to the genotype. Human recombinant FSH (Gonal-f, Merck Serono) will be self-administered sc at the dose of 150 IU every other day for 12 weeks, followed by 12 weeks of observation (follow up). Changes in sperm DFI will be the primary end point and compared between the two arms. In addition, the effects on pregnancy rate and other clinical and hormonal parameters will be evaluated.

Should this pilot, proof-of-principle trial demonstrate that the response to FSH in male idiopathic infertility depends on FSHR genotype, larger interventional trials aiming at assessing the effects on pregnancy rate will be justified.

02

Conditions studied

  • Male Infertility
03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 88 is below the median of 120 across 1,698 interventional studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Azienda USL Modena is the lead sponsor of 11 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 50 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • age 20-50 years
  • idiopathic male factor infertility for at least one year;
  • homozygous FSHR allele at codon 680 (wild type: Asn/Asn or Ser/Ser);
  • sperm DFI > 15%;
  • normal serum FSH levels (\< 8 IU/L)
  • normal serum LH, testosterone, prolactin and estradiol levels
  • normal ovulatory female partner These men might have impaired ejaculate parameters (decreased sperm count and/or decreased proportion of sperm with progressive motility and/or decreased proportion of sperm with normal morphology) of unknown aetiology.

Exclusion criteria

Exclusion Criteria:

  • azoospermia
  • all known aetiologies of male infertility (endocrine disorders, genetic disorders, chromosome abnormalities, congenital bilateral absence of the vas deferens, microdeletions within the AZF regions of the Y chromosome, varicocele, cryptorchidism, infections, immunological infertility, and obstructive infertility)
  • all known aetiologies of female infertility in the partner (tubal blockage, endocrine abnormalities including anovulation and PCO, anatomical abnormalities, infections)
  • heterozygous FSHR allele at codon 680
  • drug abuse and major systemic diseases
  • testicular insufficiency
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
88 participants (actual)

Study arms

  • Experimental
    Arm 1

    FSHR A680G SNP homozygous for allele N treated with follitropin alpha

    Drug: follitropin alpha

  • Experimental
    Arm 2

    FSHR A680G SNP homozygous for allele S treated with follitropin alpha

    Drug: follitropin alpha

Interventions

  • Drugfollitropin alpha

    All subjects included in the study will receive recombinant FSH therapy (follitropin alpha: Gonal-f 150 I.U. s.c. every other day for 12 weeks). Follow up: 12 further weeks after end of treatment. Previous studies included in the Cochrane meta-analysis used: hMG/hCG, 150 IU three times a week for 13 weeks; purified FSH, 150 IU/day for 12 weeks; rec hFSH, 150 IU/day for 12 weeks; rec hFSH, 100 IU on alternate days for 3 months. Therefore any dosage \> 100 IU on alternate days is eligible. The duration of treatment is based on the duration of one spermatogenetic cycle.

    Also known as: Gonal f

06

What researchers measure

Primary outcomes

  1. Sperm DFI

    Time frame: "after 12 weeks"

Secondary outcomes

  1. Sperm DFI (DNA Fragmentation Index)

    Time frame: "Baseline"

  2. Sperm DFI

    Time frame: "after 24 weeks"

Other outcomes

  1. Pregnancy rate

    Time frame: "baseline"

  2. Pregnancy rate

    Time frame: "After 12 weeks"

  3. Pregnancy rate

    Time frame: "after 24 weeks"

  4. Sperm count

    Time frame: "baseline"

  5. Sperm count

    Time frame: "after 12 weeks"

  6. Sperm count

    Time frame: "after 24 weeks

  7. Inhibin B

    Serum dosage

    Time frame: "baseline"

  8. Inhibin B

    Serum dosage

    Time frame: "after 12 weeks"

  9. Inhibin B

    Serum dosage

    Time frame: "after 24 weeks"

  10. Anti-Mullerian Hormone (AMH)

    Serum dosage of Anti-Mullerian Hormone

    Time frame: "baseline"

  11. AMH

    Serum dosage of Anti-Mullerian Hormone

    Time frame: "after 12 weeks"

  12. AMH

    Serum dosage of Anti-Mullerian Hormone

    Time frame: "after 24 weeks"

07

Study locations

6 sites
  • Zentrums für Reproduktions-medizin und Andrologie Universitätsklinikum Halle (Saale), Martin-Luther-Universität Halle-Wittenberg
    Halle, 06120, Germany
  • Dipartimento di Ginecologia e Medicina della Riproduzione IRCCS Istituto Clinico Humanitas,
    Rozzano, Milan 20089, Italy
  • Andrology Unit Department of Clinical Physiopathology
    Florence, 50139, Italy
  • AziendaUSLModena
    Modena, 41126, Italy
  • University of Padova Department of Histology, Microbiology and Medical Biotechnologies Clinical Pathology Section & Centre for Male Gamete Cryopreservation
    Padova, 35121, Italy
  • Department of Medical Pathophysiology, University of Rome La Sapienza, Lab of Seminology & Immunology of Reproduction
    Rome, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02349945
Lead sponsor
Azienda USL Modena
Collaborators
University of Roma La Sapienza, University of Halle Medical Faculty, Istituto Clinico Humanitas, University of Padova, University of Florence
Responsible party
Manuela Simoni (Professor, Azienda USL Modena) — Principal investigator
First posted
Jan 29, 2015
Start date
Jan 2011
Primary completion
Dec 2014
Completion
Dec 2015
Last update
Jul 12, 2016

Study contacts

Manuela Simoni, MD, PhD
principal investigator · Azienda USL Modena

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.

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