Safety and Tolerability of Lu AG06479 in Healthy Young Men

  • STATUS
    Recruiting
  • participants needed
    66
  • sponsor
    H. Lundbeck A/S
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Updated on 5 August 2020
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Summary

The purpose of this study is to investigate the safety and tolerability of Lu AG06479 and what the body does to Lu AG06479 after swallowing single doses of the drug

Description

Part A: randomized, sequential

Part B: open-label, cross-over

Details
Condition Healthy
Age 18years - 45years
Treatment Placebos, Lu AG06479
Clinical Study IdentifierNCT04473651
SponsorH. Lundbeck A/S
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Healthy, young, non-smoking men, weight 60 kg, and a body mass index (BMI) 18.5 kg/m2 and 30 kg/m2 at the Screening Visit
Other in- and exclusion criteria may apply
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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