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Study identifier: NCT05340868 Synced from ClinicalTrials.gov · July 29, 2026
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Genetics of the Acute Response to Oral Semaglutide

Condition: PreDiabetes · Prediabetic State · Obesity  ·  Sponsor: Medical University of Bialystok

PhaseNA
Planned participants1000
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The study aims to investigate the genetic basis of the response to short-term (3 months) orally administered semaglutide treatment, in terms of improving metabolic parameters, including the hormonal response to a standardized meal, and changes in body composition and liver steatosis. In the study, parameters such as fasting and 2-hour glucose during OGTT, HbA1c, body fat mass, body weight, total cholesterol, HDL and LDL, triglycerides, HOMA-IR, Matsuda Index and liver steatosis will be assessed. All the patients will undergo genome-wide genotyping. Moreover, in a subset of participants, muscle and fat biopsies will be performed, before and after the treatment, and liver, muscle and pancreas fat content will be assessed using MRI.

This description comes directly from the study's public registry record.

Talk to the study team

Lukasz Szczerbinski, MD, PhD  ·  +48858318150  ·  lukasz.szczerbinski@umb.edu.pl

Always discuss trial participation with your own doctor first.

Locations (1)

Clinical Research Centre, Medical University of BialystokBialystok, Podlaskie Voivodeship, PolandRecruiting

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Source record: clinicaltrials.gov/study/NCT05340868