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A Phase III Randomised, Double-Blind, Placebo-Controlled Multicentre Trial to Evaluate the Efficacy and Safety of AZD6234 as an Adjunct to Incretin-based Therapies in Participants with Obesity or Overweight with at Least One Weight-Related Comorbidity With or Without Type 2 Diabetes Mellitus

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523295-23-00
Enrollment
35
Registered
2026-09-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity or Overweight Weight-Related Comorbidity with/without Diabetes Mellitus, Type 2

Brief summary

Percent change in body weight from baseline at 68 weeks of treatment

Detailed description

Percent change in body weight from baseline at 68 weeks of treatment, Absolute change in weight from baseline at 68 weeks of treatment, Achievement of at least 5% body weight loss from baseline at 68 weeks of treatment, Achievement of at least 10% body weight loss from baseline at 68 weeks of treatment, Change in waist circumference from baseline at 68 weeks of treatment, Percent change in triglycerides from baseline at 68 weeks of treatment, Change in systolic blood pressure from baseline at 68 weeks of treatment, Change in HbA1c from baseline at 68 weeks of treatment, Occurrence and time to first occurrence of AE, serious AE (SAE), SAE with outcome death, AE leading to discontinuation of investigational intervention, AE leading to interruption of investigational intervention, other action taken related to investigational intervention, possibly related AE as assessed by Investigator, possibly related SAE as assessed by Investigator, Observed laboratory values change from baseline and time to first treatment emergent abnormality, Observed vital sign value (including systolic and diastolic blood pressure, pulse rate), change from baseline, and time to first treatment emergent abnormality, Observed ECG parameter, change from baseline, and time to first treatment emergent abnormality

Interventions

Sponsors

AstraZeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percent change in body weight from baseline at 68 weeks of treatment—

Secondary

MeasureTime frame
Percent change in body weight from baseline at 68 weeks of treatment, Absolute change in weight from baseline at 68 weeks of treatment, Achievement of at least 5% body weight loss from baseline at 68 weeks of treatment, Achievement of at least 10% body weight loss from baseline at 68 weeks of treatment, Change in waist circumference from baseline at 68 weeks of treatment, Percent change in triglycerides from baseline at 68 weeks of treatment, Change in systolic blood pressure from baseline at 68 weeks of treatment, Change in HbA1c from baseline at 68 weeks of treatment, Occurrence and time to first occurrence of AE, serious AE (SAE), SAE with outcome death, AE leading to discontinuation of investigational intervention, AE leading to interruption of investigational intervention, other action taken related to investigational intervention, possibly related AE as assessed by Investigator, possibly related SAE as assessed by Investigator, Observed laboratory values change from baseline and —

Outcome results

None listed

Source: EU CTIS · Data processed: Sep 22, 2026