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OsteoporosisROMIRNANCT07616401

MicroRNA and Markers and Therapeutic Response to Romosozumab and Abaloparatide in Postmenopausal Osteoporosis

A study testing miRNA typing in people with Osteoporosis and Menopause, run by Istituto Auxologico Italiano at 2 sites in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Osteoporosis is a systemic skeletal disorder affecting approximately 10% of individuals over 50 years of age. It is characterised by an increased risk of fragility fractures, which constitute a major source of morbidity, mortality, and healthcare burden worldwide. Read more about this study

Who is it for?
Ages 50 years and older, women only
Conditions the study is for
Osteoporosis, Menopause
What is being tested?
miRNA typing
Could I receive a placebo?
No, everyone receives an active treatment
How many people
42 participants
Where
2 sitesItaly
Study dates
31 Aug 2025to 31 Aug 2029
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Female sex
  • Postmenopause
  • Densitometric diagnosis of osteoporosis
  • Normal calcium diet
  • Supplement with cholecalciferol or calcifediol

Who cannot join

  • Premenopause
  • Chronic therapy with glucocorticosteroids, or other treatments that may affect bone metabolism
  • Diseases and conditions that may affect bone metabolism

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Sabrina Corbetta, Prof. contact

+3902619111

s.corbetta@auxologico.it

Italy2 sites, 2 recruiting
  • Istituto Auxologico Italiano IRCCS

    Miano, Lombardy, 20149

    Sabrina Corbetta, Prof., +39-02619111, s.corbetta@auxologico.it

    Recruiting
  • IRCCS Ospedale Galeazzi Sant'Ambrogio

    Milan, Lombardy

    Gregorio Guabello, MD, gregorio.guabello@gmail.com

    Not yet recruiting

Other trials in Italy

About this study

Official title: MicroRNA and Circulating Markers Predictive of the Therapeutic Response to Romosozumab and Abaloparatide Treatment in Women With Postmenopausal Osteoporosis

Osteoporosis is a systemic skeletal disorder affecting approximately 10% of individuals over 50 years of age. It is characterised by an increased risk of fragility fractures, which constitute a major source of morbidity, mortality, and healthcare burden worldwide.

A range of pharmacological therapies has been approved for osteoporosis, with demonstrated efficacy in reducing fracture risk. These include anabolic agents that stimulate osteoblast-mediated bone formation (teriparatide, abaloparatide), antiresorptive agents that inhibit osteoclast-driven bone resorption (bisphosphonates, denosumab), and dual-action agents such as romosozumab, which, through sclerostin inhibition, simultaneously enhances bone formation and suppresses resorption. In clinical practice, these agents are administered sequentially or in combination to optimise therapeutic outcomes.

Read more

The primary goal of anti-osteoporotic therapy is to reduce the risk of incident and subsequent fractures. In postmenopausal osteoporosis, this objective is closely linked to meaningful gains in bone mineral density (BMD), as measured by dual-energy X-ray absorptiometry (DEXA), with attainment of osteopenic ranges associated with low fracture probability (<15% for major osteoporotic fractures and <3% for hip fractures, according to FRAX). However, selecting the most effective therapeutic strategy remains challenging, as robust predictors of individual treatment response are lacking. Although bone turnover markers are widely used to monitor treatment effects, their value in predicting clinical outcomes is limited.

MicroRNAs (miRNAs) are small (~22 nucleotides), single-stranded, non-coding RNAs that regulate gene expression at the post-transcriptional level through binding to complementary sequences in target mRNAs. Circulating miRNAs are stabilised by association with proteins and extracellular vesicles, making them attractive candidates as biomarkers. Increasing evidence indicates that miRNAs play key roles in osteoblast and osteoclast differentiation, proliferation, and apoptosis, and distinct miRNA expression profiles have been associated with osteoporosis and fragility fractures.

An emerging area of interest is the interaction between osteoactive therapies and circulating miRNA signatures. To date, available data are largely limited to antiresorptive agents and teriparatide. No studies have yet addressed miRNA expression profiles in patients treated with romosozumab or abaloparatide.

Beyond miRNAs, additional molecular pathways implicated in osteoimmunological crosstalk and ageing are gaining attention as potential biomarkers. Nitric oxide (NO) plays a multifaceted role in bone homeostasis, inhibiting osteoclast activity while promoting osteoblast function. Reduced circulating NO levels have been identified as an independent predictor of osteoporotic fractures in postmenopausal women. Autophagy is increasingly recognised as a critical regulator of bone remodelling, influencing both osteoblastic and osteoclastic activity. Dysregulation of autophagic pathways disrupts bone homeostasis and contributes to bone loss. These processes are tightly controlled by complex molecular networks, including miRNAs, and are closely linked to lysosomal function. In this context, cathepsin K has emerged as a promising therapeutic target in osteoporosis.

The present study primarily aims to identify circulating microRNAs, whose early treatment-induced changes are predictive of the outcome of the therapy in terms of changes in BMD. Secondary, it aims to identify correlations of the changes in microRNAs serum concentrations with variations in biomarkers of bone metabolism as well as of aging.

The study enrols women with diagnosis of severe postmenopausal osteoporosis addressed to treatment with romosozumab or with abaloparatide. All women will be assessed at baseline and after 2, 6 and 12 months of treatment.

Being tested
miRNA typing
Keywords
Osteoporosis, Bone markers, MicroRNA, Romosozumab, Abaloparatide
Medical subject headings
Osteoporosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • miRNA typingDiagnostic test

    Identification circulating miRNAs

Study groups in NCT07616401
Study groupRoleWhat they receive
Romosozumab treatmentExperimentalPostmenopausal women treated with romosozumab for twelve months
Receives: Diagnostic Test: miRNA typing
Abaloparatide treatmentExperimentalPostmenopausal women treated with abaloparatide for twelve months
Receives: Diagnostic Test: miRNA typing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. miRNA expression profile

    Expression profile of circulating miRNA correlated to osteoporosis

    Measured: Baseline, 2, 6 and 12 months of treatment

  2. Bone Mineral Density

    Bone Mineral Density (BMD), tested via a DEXA scan and expressed in T-score

    Measured: Baseline, 2, 6 and 12 months of treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Jun 2026
  2. Study start31 Aug 2025
  3. Primary completion31 Aug 2029 (estimated)
  4. Study completion31 Aug 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
42 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07616401
Sponsor's protocol ID
32C501
Acronym
ROMIRNA
Status last verified
May 2026
First submitted
23 May 2026
Last updated
1 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing miRNA typing in people with Osteoporosis and Menopause, run by Istituto Auxologico Italiano at 2 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 1 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sabrina Corbetta, Prof. (+3902619111, s.corbetta@auxologico.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

miRNA expression profile (time frame: Baseline, 2, 6 and 12 months of treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Jun 2026.

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