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Completed Phase 2 Interventional Accepts healthy volunteers

Efficacy, Safety and Tolerability of AZD6234 in Participants Living With Overweight or Obesity With Type 2 Diabetes Who Are on a Stable Dose of GLP-1 Receptor Agonist

ClinicalTrials.gov ID: NCT06851858

Public ClinicalTrials.gov record NCT06851858. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 4:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Randomised, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of AZD6234 in Participants Living With Overweight or Obesity With Type 2 Diabetes Who Are on a Stable Dose of GLP-1 Receptor Agonist

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase II study is a randomized, parallel group, double blinded, placebo-controlled, multicenter to evaluate the efficacy, safety, and tolerability of AZD6234 in adults with overweight or obesity and type 2 diabetes on stable GLP-1 RA therapy.

Study identification

NCT ID
NCT06851858
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
69 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 12, 2025 (Actual)
Primary completion
May 26, 2026 (Actual)
Completion
May 26, 2026 (Actual)
Last update posted
Sep 24, 2026

2025 – 2026

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Research Site Birmingham Alabama 35205 —
Research Site Mobile Alabama 36608 —
Research Site Doral Florida 33166 —
Research Site Jacksonville Florida 32216 —
Research Site Miami Florida 33135 —
Research Site Miami Florida 33136 —
Research Site Winter Park Florida 32789 —
Research Site Canton Georgia 30114 —
Research Site Fayetteville Georgia 30214 —
Research Site Chicago Illinois 60640 —
Research Site Oak Brook Illinois 60523 —
Research Site Newton Kansas 67114 —
Research Site Lexington Kentucky 40509 —
Research Site Kansas City Missouri 64114 —
Research Site Las Vegas Nevada 89119 —
Research Site Norman Oklahoma 73069 —
Research Site Knoxville Tennessee 37909 —
Research Site San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06851858, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 24, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06851858 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →