drugset / Trial / NCT03182920

A Study of Lasmiditan in Healthy Participants

NCT03182920

Phase 1 Completed 35 enrolled Eli Lilly and Company
RandomizedCrossoverDouble-blindBasic science

Summary

The purpose of this study is to look at the amount of study drug that gets into the blood stream and how long it takes the body to get rid of it by comparing the results of healthy elderly participants to those of healthy young participants. The tolerability of the study drug will be evaluated. Information about any side effects that may occur will also be collected. This study will last up to approximately 19 days, not including screening. This study requires either one (Group 2) or two (Group 1) stays at the clinic each of at least four days/three nights. Participants will return for a follow-up seven days after last dose of study drug. Screening is required within 28 days prior to Day 1. This study is for research purposes only and is not intended to treat any medical condition.

Timeline

Start
2017-06-16
Primary completion
2017-08-14
Completion
2017-08-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Lasmiditan Small molecule 200 mg Oral

Indications

No indication recorded.