drugset / Trial / NCT06148272

A Study of LY3971297 in Healthy Participants

NCT06148272 ↗

Phase 1 Active not recruiting 225 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this study is to measure side effects of LY3971297 injection administered under the skin in healthy participants and obese participants with high blood pressure (BP). Blood tests will be performed to check how much LY3971297 gets into the bloodstream and how long it takes the body to eliminate it. This is a 7-part study. The study duration will be approximately 60 days for Parts A and F, and approximately 90 days for Parts B, C, D, E, and G.

Timeline

Start
2023-12-07
Primary completion
2026-08
Completion
2026-08

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3971297 Unknown — Subcutaneous
Subject LY3971297 Unknown — Intravenous