La Mesa, CANCT07684144Now EnrollingIRB Ready

Obesity Clinical Trial in La Mesa, CA

Access cutting-edge obesity treatment through this phase 3 clinical trial at a research site in La Mesa. Study-provided care at no cost to qualified participants.

Sponsored by Amgen

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Expert Care in La Mesa

Access obesity specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related obesity treatment provided free

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Check if you qualify for this obesity clinical trial in La Mesa, CA

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Why Participate?

  • No-Cost Study Care

  • Local to La Mesa

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit La Mesa site if eligible
  4. 4Begin participation

About This Obesity Study in La Mesa

The primary objective of this trial is to evaluate the long-term efficacy, safety, and tolerability of maridebart cafraglutide in participants with obesity and type 2 diabetes mellitus. Trial 20210182 is extension of trial 20210184 (NCT06858878).

Sponsor: Amgen

Who Can Participate

Inclusion Criteria

Signed informed consent form (ICF) indicating compliance with the requirements and restrictions listed in the ICF and this protocol.
Participants completing Study 20210184 must meet the following criteria:
Completed the Week 72 visit in Study 20210184.
Did not permanently discontinue the investigational product in the parent trial (20210184).
Randomized within 7 days of week 72 visit in the parent trial.
Participants must use protocol-specified contraception during treatment and for 16 weeks after the last dose of trial intervention.

Exclusion Criteria

Planned (during the trial) surgical, endoscopic, or device-based treatment for obesity.
Body mass index (BMI) ≤ 18.5 kilograms per meter square (kg/m\^2).
Participant has known sensitivity to any of the products or components to be administered during dosing.
History of ischemic optic neuropathy.
Any malignancy diagnosed during the parent trial, except for the following treated with curative intent:
Nonmelanoma skin cancers
Breast ductal carcinoma in situ
Cervical carcinoma in situ
Prostate cancer in situ
Newly identified (during the parent trial) multiple endocrine neoplasia syndrome type 2, or family history (first-degree relative\[s\]) history of medullary thyroid carcinoma (MTC).
Patient Health Questionnaire-9 (PHQ-9) score ≥ 15 at the Week 72 visit from the parent trial (20210184) before randomization.
Any suicidal ideation (category 4 or 5) or any suicidal behavior on the Columbia-Suicide Severity Rating Scale (C-SSRS), Since Last Visit version, at the Week 72 visit from the parent trial before randomization.
Participant unlikely to be able to complete all protocol-required procedures, restrictions and requirements, in the judgment of the individual and investigator.
History or evidence of any other clinically significant disorder, condition, disease (including, but not limited to known drug or alcohol abuse, eating disorders, and conditions identified during the parent trial) that, in the opinion of the investigator, would pose a risk to participant safety.
Currently pregnant (confirmed with positive pregnancy test) or breastfeeding or planning to become pregnant or breastfeed while on trial until an additional 16 weeks after the last dose of trial intervention.
Major surgical procedures planned during the trial.
Participants with minor surgical procedures (not requiring general anesthesia or deep sedation) planned during the trial may be eligible at the discretion of the investigator.
Investigative site personnel directly affiliated with the trial and/or their immediate family (ie, spouse, parent, child, or sibling, whether biological or legally adopted).

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in La Mesa?

Yes, this clinical trial (NCT07684144) has an active research site in La Mesa, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Obesity Treatment Options in La Mesa, CA

If you're searching for obesity treatment options in La Mesa, CA, this clinical trial (NCT07684144) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our La Mesa research site is actively enrolling participants for this phase 3 clinical trial. You'll receive care from experienced obesity specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all obesity clinical trials near you to find additional studies recruiting in your area.

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