Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

A Novel Aromatase Inhibitor, Leflutrozole, for Treatment of Non-Obstructive Azoospermia (NOVA-NOA)

30. april 2026 oppdatert av: Martin Blomberg Jensen

The NOVA-NOA Trial A Novel Aromatase Inhibitor, Leflutrozole, for Treatment of Non-Obstructive Azoospermia A Prospective Interventional Study

This clinical interventional study aims to assess whether treatment with with leflutrozole can improve sperm production in infertile men with non-obstructive azoospermia selected by serum anti-mullerian hormone (AMH) or Inhibin B as a positive predictive biomarker.

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Detaljert beskrivelse

Non-obstructive azoospermia (NOA) is the most severe form of male factor infertility and reflects a profound impairment of spermatogenesis. Men with NOA typically require surgical sperm retrieval procedures, such as testicular sperm aspiration (TESA), testicular sperm extraction (TESE), or micro-TESE, followed by intracytoplasmic sperm injection (ICSI). Even with surgical retrieval, sperm recovery rates remain limited and live birth rates are modest. At present, no pharmacological treatments are approved for male infertility, underscoring a substantial unmet clinical need.

Aromatase inhibitors reduce the conversion of testosterone to estradiol by inhibiting the CYP19A1 enzyme, thereby increasing the testosterone-to-estradiol ratio and stimulating gonadotropin secretion. Letrozole and anastrozole have been used off-label in infertile men, including selected patients with NOA, with small studies demonstrating that aromatase inhibition may induce the appearance of spermatozoa in the ejaculate. Leflutrozole is a novel, non-steroidal aromatase inhibitor and a derivative of letrozole with an extended half-life, allowing once-weekly oral dosing at substantially lower doses than conventional daily aromatase inhibitor regimens. Previous clinical studies in men with obesity-associated functional hypogonadism have demonstrated that once-weekly leflutrozole improves serum testosterone concentrations and semen parameters with an acceptable safety profile.

The NOVA-NOA trial is a single-center, prospective, interventional study designed to evaluate the efficacy and safety of leflutrozole in men with non-obstructive azoospermia. The study investigates whether 20 weeks of treatment with oral leflutrozole 0.3 mg administered once weekly can induce the presence of spermatozoa in the ejaculate and thereby potentially reduce the need for surgical sperm retrieval.

Following informed consent and confirmation of azoospermia at screening and baseline, eligible participants receive oral leflutrozole 0.3 mg once weekly for a total treatment duration of 20 weeks. Semen samples are collected prior to treatment and during therapy at predefined visits (Weeks 12, 16, and 20) to evaluate spermatogenic response. If spermatozoa are identified in any semen sample during treatment, participants are offered repeat semen sampling and referral to a fertility clinic for cryopreservation according to standard clinical practice. Participants continue study treatment until Week 20 irrespective of early detection of spermatozoa.

Blood and urine samples are collected longitudinally to characterize changes in reproductive hormones, metabolic parameters, mineral homeostasis, bone turnover markers, and circulating concentrations of leflutrozole. Seminal fluid is additionally analyzed for leflutrozole concentrations when sufficient ejaculate volume permits. These assessments are intended to describe the endocrine and systemic effects of sustained aromatase inhibition in men with NOA and to support mechanistic interpretation of any spermatogenic response.

Safety is evaluated throughout the study using repeated clinical assessments, laboratory monitoring, and systematic recording of adverse events. Key safety measures include monitoring of hematocrit, hemoglobin, prostate-specific antigen, liver biochemistry, and cardiovascular parameters. Participants are followed until Week 24 for on-site safety assessments, corresponding to more than five half-lives of the investigational medicinal product, and complete an additional safety and pregnancy outcome follow-up by telephone at Week 36.

Statistical analyses are conducted on an intention-to-treat basis. The primary efficacy analysis evaluates whether treatment with leflutrozole induces the presence of spermatozoa in the ejaculate, using an exact binomial testing framework under the assumption that untreated men with NOA would not spontaneously develop spermatozoa during the observation period. Secondary analyses describe within-participant changes in hormonal, metabolic, and exploratory semen parameters over time.

The overall objective of the NOVA-NOA trial is to determine whether, once-weekly leflutrozole administered without concomitant medication can induce spermatogenesis sufficient for the appearance of spermatozoa in the ejaculate of men with non-obstructive azoospermia, thereby offering a potential non-surgical pathway to biological fatherhood for a subset of this patient population.

Studietype

Intervensjonell

Registrering (Antatt)

15

Fase

  • Fase 2
  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

      • Herlev, Danmark, 2100
        • Division of Translational Endocrinology, Department of Endocrinology and Internal Medicine, Copenhagen University Hospital Herlev., Herlev,
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Signed informed consent by participant
  • Signed informed consent by participant's partner (must just be obtained before the par-ticipant starts treatment at Visit 1), if applicable, regarding blood samples, data collec-tion about fertility treatment as well as pregnancy and pregnancy outcome
  • 18-55 years
  • Azoospermia verified by at least 2 semen samples, average semen volume >= 1,0 ml with no identifiable sign of obstruction (samples taken at Visit -1 and at Visit 0 prior to confirmation of eligibility and dosing).
  • Serum AMH or Inhibin B level above the lower limit of quantification (LLOQ) at screening or within 6 months prior to screening
  • Testosterone < 15 nmol/L at screening or within 6 months prior to screening
  • Serum estradiol above the lower limit of normal range (48 pmol/L) at screening or within 6 months prior to screening

Exclusion Criteria:

  • Klinefelter or other major genetic conditions including large deletions on sex chromosomes
  • Average testis size > 20 mL unless obstruction has been excluded
  • TESE procedure < ½ year ago
  • LH concentration > 15 IU/L at screening
  • Current abuse of steroids
  • BMI > 45 kg/m2
  • Severe chronic diseases requiring daily medication
  • Prior thromboembolic event within the last 24 months
  • Cardiovascular event within the last 6 months judged as significant by the investigator
  • Osteoporosis requiring medical treatment
  • Use of any prescription or non-prescription medication (apart from routine vitamins, occasional use of paracetamol, acetylsalicylic acid, or ibuprofen) which could interfere with pharmacokinetic or pharmacodynamic results, as judged by the investigator, such as:

    • Herbal products and non-routine vitamins
    • Insulin
    • Medication such as systemic corticosteroids, tricyclic antidepressants, and atypical antipsychotics
  • Surgery scheduled for the trial duration period, except for minor, non-gastrointestinal surgical procedures at the discretion of the investigator
  • Cancer (past or present, except basal cell skin cancer or squamous cell skin cancer), which in the investigator's opinion could interfere with the results of the trial
  • Serum prostate specific antigen (PSA) > 3 ng/mL at screening or within 6 months prior to screening
  • Hematocrit >50% at screening or within 6 months prior to screening
  • Mental incapacity, language barriers or unwillingness to comply with the requirements of the protocol, which may preclude adequate understanding or co-operation during the trial, as judged by the investigator

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Leflutrozole
once-weekly oral Leflutrozole capsule 0.3 mg
Leflutrozole capsule 0.3 mg once weekly administered orally

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Proportion of patients with spermatozoa in the ejaculate at Week 12-20.
Tidsramme: From enrollment to Week 20 (end-of-treatment)
The primary endpoint is proportion of patients with spermatozoa in the ejaculate at Week 20 (end-of-treatment).
From enrollment to Week 20 (end-of-treatment)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in serum reproductive hormones
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), total testosterone, estradiol, inhibin B, anti-Müllerian hormone (AMH), and sex hormone-binding globulin (SHBG).
Change from baseline to week 20 (end-of-treatment)
Change in seminal fluid reproductive biomarkers
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in concentrations of RANK ligand (RANKL), osteoprotegerin (OPG), anti-Müllerian hormone (AMH), and inhibin B measured in seminal
Change from baseline to week 20 (end-of-treatment)
Change in reproductive hormone ratios
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum inhibin B/FSH ratio, testosterone/LH ratio, testosterone/estradiol ratio, and AMH/testosterone ratio.
Change from baseline to week 20 (end-of-treatment)
Change in body mass index
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in body mass index (BMI) weight and height will be combined to calculate BMI in kg/m^2
Change from baseline to week 20 (end-of-treatment)
Change in glycemic and insulin resistance markers
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in HbA1c, fasting plasma glucose, fasting insulin, C-peptide, and homeostatic model assessment for insulin resistance (HOMA-IR)
Change from baseline to week 20 (end-of-treatment)
Change in lipid profile
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides.
Change from baseline to week 20 (end-of-treatment)
Change in hematocrit
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in hematocrit measured as a safety-related secondary outcome
Change from baseline to week 20 (end-of-treatment)
Change in markers of bone turnover
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum procollagen type 1 N-terminal propeptide (PINP) and C-terminal telopeptide of type I collagen (CTX).
Change from baseline to week 20 (end-of-treatment)
Change in urinary mineral homeostasis
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in spot urine concentrations of albumin, calcium, magnesium, iron, ferritin, phosphate, zinc, bicarbonate, and citrate.
Change from baseline to week 20 (end-of-treatment)
Change in serum mineral homeostasis
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum concentrations of albumin, calcium, phosphate, magnesium, iron, ferritin, transferrin, hepcidin, and zinc
Change from baseline to week 20 (end-of-treatment)
Change in seminal fluid mineral concentrations
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in seminal fluid concentrations of albumin, calcium, phosphate, magnesium, iron, ferritin, and zinc
Change from baseline to week 20 (end-of-treatment)
Change in calciotropic hormones
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum parathyroid hormone (PTH), fibroblast growth factor-23 (FGF-23), and α-Klotho.
Change from baseline to week 20 (end-of-treatment)
Change in vitamin D metabolites
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum concentrations of cholecalciferol, 25-hydroxyvitamin D (25-OHD), 24,25-dihydroxyvitamin D, 1,25-dihydroxyvitamin D, and derived vitamin D metabolite ratios
Change from baseline to week 20 (end-of-treatment)
Change in adrenal and androgen precursor hormones
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in serum concentrations of androstenedione, cortisone, and dehydroepiandrosterone sulfate (DHEAS).
Change from baseline to week 20 (end-of-treatment)
Leflutrozole concentrations in serum in participants
Tidsramme: From enrollment to the end of trial at 24 weeks
Plasma concentration of Leflutrozole in participants
From enrollment to the end of trial at 24 weeks
Leflutrozole concentration in seminal fluid
Tidsramme: From enrollment to the end-of-treatment at 20 weeks
Leflutrozole concentration in seminal fluid
From enrollment to the end-of-treatment at 20 weeks
Leflutrozole concentration in partners
Tidsramme: From enrollment to week 16 after inclusion
Plasma Leflutrozole concentration in the female partner
From enrollment to week 16 after inclusion
Change in sperm parameters when measurable
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in sperm count, concentration, motility, and morphology in participants with detectable spermatozoa in the ejaculate.
Change from baseline to week 20 (end-of-treatment)
Change in height
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in height (centimeters)
Change from baseline to week 20 (end-of-treatment)
Change in weight
Tidsramme: Change from baseline to week 20 (end-of-treatment)
Change in weight (kilograms)
Change from baseline to week 20 (end-of-treatment)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Martin Blomberg Jensen, D.M.Sc., Herlev Hospital

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. mai 2026

Primær fullføring (Antatt)

31. mai 2027

Studiet fullført (Antatt)

31. august 2027

Datoer for studieregistrering

Først innsendt

16. april 2026

Først innsendt som oppfylte QC-kriteriene

30. april 2026

Først lagt ut (Faktiske)

6. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. april 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere