LY4329090 for Obesity

Not yet recruiting at 2 trial locations

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug, LY4329090, as a potential treatment for obesity, to assess its tolerance and side effects in individuals who are overweight or have obesity. Blood tests will help researchers understand how the body processes this drug. Participants will be divided into two groups, each with different lengths of stay and visits to the research center. The trial suits those who are healthy, have a BMI between 27 and 40, and have maintained a stable weight for at least three months. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new drug.

Is there any evidence suggesting that LY4329090 is likely to be safe for humans?

A previous study administered LY4329090 to individuals with obesity to assess its safety. The study examined side effects and how the body processes the drug. Although detailed results from this study aren't publicly available, the treatment is currently in Phase 1 trials. Phase 1 trials represent the first stage of testing a new treatment in humans, primarily to ensure safety. This phase indicates limited information on how well people tolerate LY4329090, but it has passed initial safety tests in labs or with animals. Researchers closely monitor participants in these trials for any side effects, and the results provide insights into the drug's safety.12345

Why do researchers think this study treatment might be promising for obesity?

Unlike the standard obesity treatments, which often involve lifestyle changes or medications that suppress appetite, LY4329090 offers a novel approach by being administered subcutaneously (under the skin). This delivery method can enhance the precision and effectiveness of the treatment. Researchers are excited about LY4329090 because it may provide a more targeted and efficient way to manage obesity, potentially offering benefits over existing oral medications or surgical options. With its unique administration and potential for improved outcomes, LY4329090 could represent a significant advancement in obesity management.

What evidence suggests that LY4329090 might be an effective treatment for obesity?

Research has shown that LY4329090 is under study for its potential to aid weight loss in people with obesity. In this trial, participants will receive either LY4329090 or a placebo to assess its effectiveness. While limited data exists on its efficacy in humans, researchers are investigating it due to its promising mechanism of action. LY4329090 may assist by influencing metabolism and appetite, both crucial for managing obesity. Early tests with similar treatments have demonstrated weight reduction by targeting these areas. The hope is that LY4329090 will yield similar results and provide a new option for weight management.1467

Who Is on the Research Team?

C1

Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)

Principal Investigator

Eli Lilly and Company

Are You a Good Fit for This Trial?

This trial is for adults who are overweight or have obesity but are otherwise healthy. People with other significant health problems or conditions that could interfere with the study cannot participate.

Inclusion Criteria

Are overtly healthy with no comorbidities related to body mass index (BMI)
Have a BMI between 27.0 kilograms per square meter (kg/m²) and 40.0 kg/m², inclusive
Have had a self-reported stable weight for 3 months prior to screening
See 1 more

Exclusion Criteria

I have been diagnosed with abnormal calcium levels.
I have taken incretin drugs in the last 90 days.
Have an abnormal blood pressure and/or pulse rate at screening
See 16 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment Part A

Participants receive either LY4329090 or placebo administered subcutaneously. The study lasts about 10 weeks, including a 5-night stay in the Clinical Research Unit (CRU) and 5 outpatient visits.

10 weeks
5-night stay, 5 outpatient visits

Treatment Part B

Participants receive either LY4329090 or placebo administered subcutaneously. The study lasts about 21 weeks, including 4 stays totaling 11 nights and 14 outpatient visits to the CRU.

21 weeks
11-night stay, 14 outpatient visits

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • LY4329090

Trial Overview

The study is testing a new drug called LY4329090 compared to a placebo (inactive substance) in people with obesity or overweight. Participants will be randomly assigned to receive either the drug or placebo, and their responses will be monitored over several weeks.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Placebo Group

Group I: Placebo Part AExperimental Treatment1 Intervention
Group II: LY4329090 Part BExperimental Treatment1 Intervention
Group III: LY4329090 Part AExperimental Treatment1 Intervention
Group IV: Placebo Part BPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Eli Lilly and Company

Lead Sponsor

Trials
2,708
Recruited
3,720,000+
Dr. Daniel Skovronsky profile image

Dr. Daniel Skovronsky

Eli Lilly and Company

Chief Medical Officer since 2018

MD from Harvard Medical School

David A. Ricks profile image

David A. Ricks

Eli Lilly and Company

Chief Executive Officer since 2017

BSc from Purdue University, MBA from Indiana University

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