Separate and Combined Extrapancreatic Effects of GIP and GLP-1

Last updated: September 8, 2025
Sponsor: University Hospital, Gentofte, Copenhagen
Overall Status: Completed

Phase

N/A

Condition

Diabetes And Hypertension

Diabetes Mellitus, Type 2

Diabetes Mellitus Types I And Ii

Treatment

Intravenous Infusion

Clinical Study ID

NCT06895408
101292 (H-21035117)
  • Ages 30-75
  • All Genders

Study Summary

The two gut-derived hormones, glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1 (GLP-1) are secreted from intestinal cells in relation to a meal and increase insulin secretion from the pancreas. The hormones also exert effects outside the pancreas, but especially for GIP, these are poorly investigated. Because of this, only GLP-1 based drugs (GLP-1 receptor agonists) are on the market for the treatment of type 2 diabetes and obesity. Nonetheless, a new drug is in clinical development: a combined GIP-GLP-1-receptor agonist (tirzepatide), which has shown better results than GLP-1 alone. The mechanism behind these impressive effects are unknown and in this study, the investigators will look into the exptrapancreatic effects of GIP and GLP-1, separate and combined and thus elucidate the mechanisms of action of this new drug class.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Total pancreatectomy

  • Caucasians between 30-75 years of age

  • Blood haemoglobin >7.0 mmol/l for males and >6.5 mmol/l for females

Exclusion

Exclusion Criteria:

  • Pancreatectomy within the last 3 months

  • Ongoing chemotherapy or chemotherapy within the last 3 months

  • Treatment with GLP-1 receptor agonists within the last 3 months

  • Renal impairment (estimated by estimated glomerular filtration rate (eGFR) <60ml/min/1.73 m2) and/or albuminuria

  • Calcium related disease, hypo-/hyperthyroidism

  • Known significant liver disease, plasma alanine aminotransferase (ALT) or aspartateaminotransferase (AST) ≥3 × normal value or INR (The international normalised ratiobased on prothrombin time) outside the normal range

  • Severe arteriosclerotic heart disease or heart failure (New York Heart Association (NYHA) group III or IV)

  • Pregnancy and/or breastfeeding

  • Use of more than 14 units of alcohol per week or abuse of narcotics

  • Any condition that the investigator feels would interfere with trial participation

Study Design

Total Participants: 12
Treatment Group(s): 1
Primary Treatment: Intravenous Infusion
Phase:
Study Start date:
February 19, 2025
Estimated Completion Date:
July 14, 2025

Connect with a study center

  • Center for Clinical Metabolic Research, Gentofte Hospital

    Hellerup, 2900
    Denmark

    Site Not Available

  • Center for Clinical Metabolic Research, Gentofte Hospital

    Hellerup 2620516, 2900
    Denmark

    Site Not Available

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