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NCT06595238CompletedPhase 2

A Study in Participants With Obesity or Overweight With at Least One Weight-related Comorbidity

A Phase IIb Randomised, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of AZD6234 in Participants Living With Obesity or Overweight With Comorbidity

Source: ClinicalTrials.gov · Last updated 2 Oct 2026

Brief summary (registry, in English)

A Phase IIb Randomised, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of AZD6234 compared with placebo, given once a week as subcutaneous injection for 36 weeks, in male and female participants of at least 18 years of age who are living with obesity (body mass index \[BMI\] ≥ 30 kg/m2), or overweight (BMI ≥ 27 kg/m2) and at least one weight-related comorbidity

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
262 (actual)
First submitted
11 Sept 2024
Start date
1 Oct 2024
Primary completion date
3 Dec 2025
Lead sponsor
AstraZeneca
Diseases
Obesity
NCT number
NCT06595238
EU CT number
2024-514000-13-00

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 262
  • From 1 Oct 2024 to the primary completion date, 3 Dec 2025
  • 39 sites in 5 countries
  • 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 prescription or non-prescription medication for weight loss within the last 3 months prior to Screening
  • Previous or planned (within study period) bariatric surgery or fitting of a weight loss device (eg, gastric balloon or duodenal barrier)

Other illness

  • Have obesity induced by other endocrine disorders, such as Cushing's syndrome or Prader-Willi syndrome
  • History of type 1 diabetes mellitus or T2DM

Who the study is looking for

  • Adults ≥ 18 years of age
  • BMI of (a) ≥ 30 kg/m2, or (b) ≥ 27kg/m2 and have a current diagnosis of at least 1 weight-related comorbidities (treated or untreated)
  • A stable body weight for 3 months prior to Screening (±5% body weight change)

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (39)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
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HeidelbergAustraliaUnknown status
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MaroochydoreAustraliaUnknown status
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MaroubraAustraliaUnknown status
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MerewetherAustraliaUnknown status
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HamiltonCanadaUnknown status
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MontrealCanadaUnknown status
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SarniaCanadaUnknown status
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SherbrookeCanadaUnknown status
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StouffvilleCanadaUnknown status
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TorontoCanadaUnknown status
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HullUnited KingdomUnknown status
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LeicesterUnited KingdomUnknown status
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PenarthUnited KingdomUnknown status
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RotherhamUnited KingdomUnknown status
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ChūōkuJapanUnknown status
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Shinjuku-kuJapanUnknown status
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Suita-shiJapanUnknown status
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AustinUnited StatesUnknown status
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DallasUnited StatesUnknown status
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GulfportUnited StatesUnknown status
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HialeahUnited StatesUnknown status
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IndianapolisUnited StatesUnknown status
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Kansas CityUnited StatesUnknown status
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KnoxvilleUnited StatesUnknown status
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LargoUnited StatesUnknown status
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Long BeachUnited StatesUnknown status
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Lutherville-TimoniumUnited StatesUnknown status
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MobileUnited StatesUnknown status
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North CharlestonUnited StatesUnknown status
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OmahaUnited StatesUnknown status
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OrlandoUnited StatesUnknown status
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PhoenixUnited StatesUnknown status
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Port ArthurUnited StatesUnknown status
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PortsmouthUnited StatesUnknown status
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RidgelandUnited StatesUnknown status
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San AntonioUnited StatesUnknown status
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StatesvilleUnited StatesUnknown status
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TampaUnited StatesUnknown status
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WoodstockUnited StatesUnknown status

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