← Eichor
Study identifier: NCT05071898 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pharmacogenetics of Response to GLP1R Agonists

Condition: Obesity · Diabetes Type 2  ·  Sponsor: University of Maryland, Baltimore

PhasePhase 1
Planned participants600
Who can joinAll sexes, 18 Years to 89 Years
Healthy volunteersYes

About this study

Overweight/obese otherwise healthy volunteers will be recruited from the Old Order Amish population in Lancaster County, PA. Lancaster County, PA. Pharmacodynamic responses to GLP1R agonist will be assessed by conducting frequently sampled intravenous glucose tolerance tests (FSIGT) both before and after semaglutide for six weeks. The proposal proposes two specific aims: 1. Specific Aim #1. To identify genetic variants associated with effects of a GLP1R agonist to enhance glucose-stimulated first phase insulin secretion in the two FSIGTs (before and after administration of drug). 2. Specific Aim #2. To identify genetic variants associated with the effect of a GLP1R agonist to accelerate the rate of glucose disappearance as assessed in the two FSIGTs (before and after administration of drug). Genotyping will be conducted using a high-density array with comprehensive coverage of DNA sequence variants. In addition, the analysis will leverage a global imputation panel generated from 1,025 Amish individuals.

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

Talk to the study team

Amber L Beitelshees, PharmD  ·  (410)706-0118  ·  abeitels@som.umaryland.edu

Simeon I Taylor, MD, PhD  ·  (410)706-6439  ·  staylor2@som.umaryland.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Amish Research ClinicLancaster, Pennsylvania, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05071898