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Clinical Trials in Denmark / NCT06790225
Recruiting Not applicable

Glucose-dependent INsulinotropic Polypeptide: Effect on Bone Remodelling and Cell Activity (GINEBRA)

NCT06790225 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2025-11-10
Last updated
2026-01-02

Condition(s) studied

Bone Disease, MetabolicDiabetes Mellitus, Type 2Obesity and Obesity-related Medical Conditions

Investigational drug(s) / intervention(s)

Glucose-dependent Insulinotropic Polypeptide (GIP)

Glucose-dependent Insulinotropic Polypeptide (GIP): Recombinant human GIP (1-42)

Study summary

Glucose-dependent insulinotropic polypeptide (GIP) is released by the intestines in response to food intake and increases insulin secretion. Although short-term (\< 3 hours) stimulation with GIP decreases bone resorption in humans, the effect may vanish following continuous administration within 24 hours, at least in patients with type 1 diabetes. Whether the anti-resorptive effect of GIP can be maintained if the hormone is non-continuously administrated is unclear. As the first GIP receptor (GIPR) agonist, tirzepatide was recently approved for the treatment of obesity and type 2 diabetes in the USA and type 2 diabetes alone in the EU, there is a need to establish knowledge about the long-term effects of GIP on bone health, including if different exposure times to GIP have different skeletal effects.

This project will investigate whether GIP maintains its anti-resorptive potential if given as intermittent compared to continuous infusion in healthy men and women aged 18-40 years. Administration cycles involve intermittent (8 hours daily) and continuous (24 hours daily) injection of GIP for three days each. The effect of GIP will be measured by bone markers in blood samples, as well as in vitro activity and genetic alterations of bone cells (osteoclasts and osteoblasts) using bone marrow aspirates and bone marrow biopsies. Each participant will receive both administration cycles using a crossover design with a 14-28 days washout period between administrations of GIP.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: * healthy volunteers Exclusion Criteria: * pre-diabetes or diabetes (HbA1c \>42mmol/mol) * BMI \>28 * fractures with \< 6months * comorbidities/treatments that may influence bone metabolism or procedures - -- pregnancy * inability to provide informed concent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University hospital of Southern Denmark Esbjerg Denmark Recruiting

More Esbjerg Hospital - University Hospital of Southern Denmark trials in Denmark

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06790225 on ClinicalTrials.gov ↗ ← All trials in Denmark