Healthy Clinical Trial - A Study of Baricitinib in Healthy Participants

Status Completed

Clinical Trial Summary

The purposes of this study are to determine:

- If there are any differences in the amount of baricitinib in the blood/body when taken in two different forms.

- How a high-fat, high-calorie meal affects the amount of baricitinib in the blood/body.

- The safety and tolerability of baricitinib.

The study has two parts. Individuals will participate in only one part.

Participants will be admitted to the clinical research unit (CRU) and will be discharged from the CRU following the completion of 3 overnight stays.

Each part of this study will last from 8-10 days, not including screening. Follow-up will occur 7 to 14 days after the last dose of baricitinib.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Healthy

Clinical Trial Details

NCT number	NCT03212638
Study type	Interventional
Source	Eli Lilly and Company
Contact
Status	Completed
Phase	Phase 1
Start date	June 27, 2017
Completion date	November 1, 2017

View Details

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