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Clinical Trial Summary

The purpose of this study is to investigate the safety of multiple oral doses of Lu AG06474, how well the doses are tolerated, and what the body does to the drug after administering it to healthy young participants. This study also aims to compare how the body absorbs and uses Lu AG06474 when it is given in capsule form versus when it is given as an oral solution.


Clinical Trial Description

The study has 2 parts: Part A and Part B. Part A consists of up to 7 sequential cohorts (Cohorts A1 to A7), with 8 participants per cohort randomized to receive multiple doses of either Lu AG06474 or placebo: 6 will receive Lu AG06474 oral solution and 2 will receive placebo. Part B consists of 1 cohort (Cohort B1), with 12 participants: all participants will receive 2 single doses of Lu AG06474 (one as an oral solution and one in capsule form), taken 3 days apart. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05943327
Study type Interventional
Source H. Lundbeck A/S
Contact Email contact via H. Lundbeck A/S
Phone +45 36301311
Email LundbeckClinicalTrials@Lundbeck.com
Status Recruiting
Phase Phase 1
Start date June 28, 2023
Completion date August 15, 2024

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