LY3502970 (Part B) for Healthy Subjects

LabCorp CRU, Inc., Madison, WI
Healthy Subjects+1 More ConditionsLY3502970 - Drug
Eligibility
18 - 70
All Sexes
What conditions do you have?
Select

Study Summary

This trial tests how well a drug, LY3502970, is absorbed and eliminated in overweight and obese patients and if it's safe and tolerated. It also looks at how food affects it. 135 days total.

Eligible Conditions
  • Healthy Subjects
  • Obesity

Treatment Effectiveness

Phase-Based Effectiveness

1 of 3
Phase 1

Study Objectives

3 Primary · 3 Secondary · Reporting Duration: Predose up to 92 days postdose

Day 92
PK: AUC[0-24] of LY3502970 in fed state
PK: Cmax of LY3502970 in fed state
PK: Maximum Observed Concentration (Cmax) of LY3502970
PK: Time to Maximum Observed Concentration (Tmax) of LY3502970
PK: Tmax of LY3502970 in fed state
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve from Time Zero to the 24 Hour Time Point (AUC[0-24]) of LY3502970

Trial Safety

Phase-Based Safety

1 of 3

Awards & Highlights

No Placebo Group
All patients enrolled in this trial will receive the new treatment.

Trial Design

2 Treatment Groups

LY3502970 (Part B)
1 of 2
LY3502970 (Part A)
1 of 2

Experimental Treatment

50 Total Participants · 2 Treatment Groups

Primary Treatment: LY3502970 (Part B) · No Placebo Group · Phase 1

LY3502970 (Part B)
Drug
Experimental Group · 1 Intervention: LY3502970 · Intervention Types: Drug
LY3502970 (Part A)
Drug
Experimental Group · 1 Intervention: LY3502970 · Intervention Types: Drug
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
LY3502970
2021
Completed Phase 2
~1160

Trial Logistics

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: predose up to 92 days postdose

Who is running the clinical trial?

Eli Lilly and CompanyLead Sponsor
2,497 Previous Clinical Trials
3,153,469 Total Patients Enrolled
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)Study DirectorEli Lilly and Company
1,278 Previous Clinical Trials
379,919 Total Patients Enrolled

Eligibility Criteria

Age 18 - 70 · All Participants · 3 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:

Frequently Asked Questions

Does the experimental program accept individuals below the age of sixty-five?

"According to the eligibility requirements of this trial, individuals between 18 and 70 are considered fit for participation. For those under eighteen or over 65 years old there are 114 studies available while 574 can be found respectively." - Anonymous Online Contributor

Unverified Answer

Are there still enrollment opportunities in this research endeavor?

"As evidenced on clinicaltrials.gov, the recruitment phase of this study has concluded; it was initially posted to the website on April 27th 2023 and last updated 24 days later. Although there are no longer any vacancies for this particular trial, 1144 other medical studies have open positions available at present." - Anonymous Online Contributor

Unverified Answer

Are there any limitations on who may participate in this experiment?

"To qualify for this research initiative, volunteers must be in good health and between the ages of 18-70. Approximately 50 individuals are needed to fulfill the trial's requirements." - Anonymous Online Contributor

Unverified Answer

What safety data is available for LY3502970 (Part A) in clinical trials?

"Due to the minimal amount of information available on LY3502970 (Part A), our team at Power have given it a safety rating of 1. This is because this trial is only in Phase 1, thus there are limited results regarding its efficacy and safety profile." - Anonymous Online Contributor

Unverified Answer
Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.