A Study of LY3410738 in Healthy Adult Participants
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy
In brief
The main purpose of this study is to assess the safety and tolerability of LY3410738 and to look at the amount of the study drug, LY3410738, that gets into the blood stream and how long it takes the body to get rid of it when given in healthy adult participants. For each participant, the total duration of the study will be 53 days, including screening.
Key facts
- Study ID
- NCT06181045
- Run by
- Eli Lilly and Company
- People needed
- 42
- Starts
- 2021-02-24
- Expected to finish
- 2021-08-04
- Last updated by the study team
- 2023-12-26
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must have Body mass index (BMI) within the range of 18.0 to 32.0 kilograms per square meter (kg/m²), inclusive
- Male and female participants in good health, determined by no clinically significant findings from medical history, 12-lead Electrocardiogram (ECG), vital sign measurements, or clinical laboratory evaluations as assessed by the investigator
- Female participants of non-childbearing potential and male participants who follow standard contraceptive methods
- Must comply with all study procedures, including the 3-night stay at the Clinical Research Unit (CRU) and follow-up phone call
You may not qualify if…
- History or presence of any diseases or conditions of clinical significance by the Investigator (or designee) and/or Sponsor
- Positive serologic test for hepatitis B surface antigen (HBsAg), hepatitis B virus immunoglobulin M (HBV IgM) core antibody, hepatitis C virus (HCV) antibody, or human immunodeficiency virus (HIV) antibody at Screening.
- Positive polymerase chain reaction (PCR) test for COVID-19 at Screening
- Known ongoing alcohol and/or drug abuse within 2 years prior to Screening
- History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee)
- Have previously received LY3410738 in any other study investigating LY3410738, within 30 days prior to Day 1
Where it is running
- Covance Clinical Research Unit — Daytona Beach, Florida, United States
- Covance Clinical Research Unit — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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