RecruitingPhase 3NCT07776509

A Study to Evaluate Effect of AZD6234 as an Adjunct to Incretin-based Therapies in Adult Participants With Obesity or Overweight With Weight-related Comorbidity With or Without Type 2 Diabetes Mellitus

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 (SELENE 3)


Sponsor

AstraZeneca

Enrollment

500 participants

Start Date

Aug 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The study will evaluate how well AZD6234 works and how safe it is in adults with excess weight or obesity. Efficacy of AZD6234 will be compared to placebo in percent body weight change from baseline at 68 weeks of treatment.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called AZD6234 and a drug called Placebo for people with obesity or overweight, weight-related comorbidity, and other related conditions. The study is currently recruiting participants at 96 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAZD6234

IMP injected subcutaneously, once a week.

DRUGPlacebo

Placebo matching IMP dose injected subcutaneously, once a week.


Locations(96)

Research Site

Escondido, California, United States

Research Site

Lincoln, California, United States

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Walnut Creek, California, United States

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Fleming Island, Florida, United States

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Jacksonville, Florida, United States

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Stockbridge, Georgia, United States

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Woodstock, Georgia, United States

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Champaign, Illinois, United States

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Chicago, Illinois, United States

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Beltsville, Maryland, United States

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Oxon Hill, Maryland, United States

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Kansas City, Missouri, United States

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Las Vegas, Nevada, United States

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Somerset, New Jersey, United States

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Statesville, North Carolina, United States

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Fargo, North Dakota, United States

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Columbus, Ohio, United States

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Portland, Oregon, United States

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Smithfield, Pennsylvania, United States

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Franklin, Tennessee, United States

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Houston, Texas, United States

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Manassas, Virginia, United States

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Renton, Washington, United States

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Buenos Aires, Argentina

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CABA, Argentina

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Ciudad de Buenos Aires, Argentina

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Ramos Mejía, Argentina

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Rosario, Argentina

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San Nicolás, Argentina

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Belo Horizonte, Brazil

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Campinas, Brazil

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Campinas, Brazil

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São Paulo, Brazil

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São Paulo, Brazil

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São Paulo, Brazil

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Calgary, Alberta, Canada

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Calgary, Alberta, Canada

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Surrey, British Columbia, Canada

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Vancouver, British Columbia, Canada

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Guelph, Ontario, Canada

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Hamilton, Ontario, Canada

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Stouffville, Ontario, Canada

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Toronto, Ontario, Canada

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Joliette, Quebec, Canada

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Montreal, Quebec, Canada

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Beijing, China

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Changchun, China

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Chengdu, China

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Chengdu, China

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Guangzhou, China

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Huzhou, China

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Nanjing, China

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Nanjing, China

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Ningbo, China

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Aarhus N, Denmark

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Gandrup, Denmark

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Herlev, Denmark

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Herlev, Denmark

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Holbæk, Denmark

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Hvidovre, Denmark

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Middelfart, Denmark

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Odense, Denmark

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Vejle, Denmark

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Holon, Israel

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Jerusalem, Israel

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Kfar Saba, Israel

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Petah Tikva, Israel

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Petah Tikva, Israel

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Tel Aviv, Israel

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Chūōku, Japan

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Ichinomiya-shi, Japan

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Izunokuni-shi, Japan

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Kamakura-shi, Japan

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Kawagoe-shi, Japan

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Kitakyushu-shi, Japan

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Kyoto, Japan

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Kyoto, Japan

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Mito, Japan

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Nishinomiya-shi, Japan

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Ōmihachiman, Japan

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Yokohama, Japan

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Linköping, Sweden

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Lund, Sweden

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Mölndal, Sweden

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Örebro, Sweden

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Stockholm, Sweden

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Ankara, Turkey (Türkiye)

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Ankara, Turkey (Türkiye)

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Antalya, Turkey (Türkiye)

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Center, Turkey (Türkiye)

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Istanbul, Turkey (Türkiye)

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Airdrie, United Kingdom

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Chippenham, United Kingdom

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Hull, United Kingdom

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Llandough, United Kingdom

Research Site

Rotherham, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT07776509


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