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NCT06851858CompletedPhase 2

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

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

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
69 (actual)
First submitted
13 Feb 2025
Start date
12 Mar 2025
Primary completion date
26 May 2026
Lead sponsor
AstraZeneca
NCT number
NCT06851858

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 69
  • From 12 Mar 2025 to the primary completion date, 26 May 2026
  • 17 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has received treatment with prescription or non-prescription medication for weight loss within the last 3 months prior to screening (other than a GLP-1 RA).
  • Self-reported weight change of \> 5 % in the 3 months prior to screening.
  • Use of insulin therapy for T2DM
  • Previous or planned (within study period) bariatric surgery or fitting of a weight loss device (eg, gastric balloon or duodenal barrier)

Other illness

  • Diabetes mellitus that is not clearly type 2 diabetes.

Lab values

  • Significant hepatobiliary disease (except for non-alcoholic steatohepatitis or nonalcoholic fatty liver disease without portal hypertension or cirrhosis)
    • 8\. Impaired renal function defined as eGFR ≤ 45 mL/minute/1.73m2 at screening

Who the study is looking for

  • Be 18 to 75 years old at the time of signing the informed consent.
  • Diagnosed with type 2 diabetes ≥ 180 days before screening.
  • HbA1c value at screening of ≥ 6.0% (42 mmol/mol) and ≤ 10% (86 mmol/mol).
  • On a stable maintenance dose of an injectable GLP-1 RA.
  • At Screening, have a BMI ≥ 27 kg/m2

Age in the registry: 18 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (17)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BirminghamUnited StatesUnknown status
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CantonUnited StatesUnknown status
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ChicagoUnited StatesUnknown status
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DoralUnited StatesUnknown status
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FayettevilleUnited StatesUnknown status
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JacksonvilleUnited StatesUnknown status
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Kansas CityUnited StatesUnknown status
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KnoxvilleUnited StatesUnknown status
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Las VegasUnited StatesUnknown status
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LexingtonUnited StatesUnknown status
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MiamiUnited StatesUnknown status
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MobileUnited StatesUnknown status
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NewtonUnited StatesUnknown status
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NormanUnited StatesUnknown status
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Oak BrookUnited StatesUnknown status
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San AntonioUnited StatesUnknown status
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Winter ParkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.