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NCT07784725 · AstraZeneca

A Study to Evaluate Effect of AZD6234 in Adult Participants With Obesity or Overweight With Weight-related Comorbidity Without Type 2 Diabetes Mellitus

(SELENE 1)

What this study is about

The study will evaluate how well AZD6234 works and how safe it is in adults with excess weight or obesity.

View original scientific description

The study will evaluate how well AZD6234 works and how safe it is in adults with excess weight or obesity.

Interventions

DRUG

AZD6234

IMP injected subcutaneously, once a week. Unit dose strength as per CSP.

DRUG

Placebo

Placebo matching IMP dose injected subcutaneously, once a week.

Primary outcome measures

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

Time frame: 68 weeks

To evaluate the effect of AZD6234 as compared to placebo in percent body weight change

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Males \& females (inclusive of all gender identities) age ≥18 years
  • BMI ≥30 kg/m2 OR BMI ≥27 kg/m2 with at least one of the following weight related comorbidities (treated or untreated): hypertension, dyslipidaemia, obstructive sleep apnoea, cardiovascular disease, heart failure, chronic kidney disease, metabolic dysfunction-associated steatotic liver disease, osteoarthritis of the knee, or stress urinary incontinence
  • Stable body weight (≤5% body weight change) for at least 3 months prior to Randomisation
  • History of at least one self-reported unsuccessful attempt to lose body weight in their lifetime

Exclusion criteria

  • Obesity primarily caused by other endocrine disorders
  • History of Type 1 or Type 2 Diabetes Mellitus, HbA1c ≥6.5% (48 mmol/mol), and/or treatment with glucose-lowering agent(s) within 3 months prior to Screening
  • Significant hepatobiliary disease and/or any of the following results at Screening:
  • ALT ≥ 3.0 × ULN
  • AST ≥ 3.0 × ULN
  • TBL \> 1.5 × ULN (except for cases of known Gilbert's Syndrome)
  • Has received treatment with a GLP-1 receptor agonist or GLP-1 containing medication for any indication within 3 months before Randomisation.

Where

  • Dothan, Alabama
  • Huntsville, Alabama
  • Mesa, Arizona
  • Escondido, California
  • Clearwater, Florida
  • Jacksonville, Florida
  • Stockbridge, Georgia
  • Champaign, Illinois
  • Chicago, Illinois
  • Ames, Iowa
  • Troy, Michigan
  • Jefferson City, Missouri

And 21 more locations — see the full list below.

Related conditions & keywords

Obesity or OverweightObesityOverweightAZD6234

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Aug 25, 2026 · Source of record for eligibility and locations

📊
1 of 2500 participants interested
0% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

NOT_YET_RECRUITING

Dothan

Alabama

Location available
NOT_YET_RECRUITING

Huntsville

Alabama

Location available
NOT_YET_RECRUITING

Mesa

Arizona

Location available
View Mesa location page
NOT_YET_RECRUITING

Escondido

California

Location available
NOT_YET_RECRUITING

Clearwater

Florida

Location available
NOT_YET_RECRUITING

Jacksonville

Florida

Location available
NOT_YET_RECRUITING

Stockbridge

Georgia

Location available
NOT_YET_RECRUITING

Champaign

Illinois

Location available
NOT_YET_RECRUITING

Chicago

Illinois

Location available

And 24 more locations available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

Find More Obesity Trials by City

Browse all obesity clinical trials in these cities — not just this study.

Browse More Trials by Condition

Looking for Obesity or Overweight Treatment in Dothan?

Join others in Alabama exploring innovative treatment options through clinical research

Obesity or Overweight Treatment Options in Dothan, Alabama

If you're searching for Obesity or Overweight treatment in Dothan, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Dothan, Huntsville, Mesa and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Obesity or Overweight. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Alabama
Now Enrolling
Up to 2500 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Obesity or Overweight?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Obesity or Overweight

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Obesity or Overweight Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07784725. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.