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Clinical Trial Summary

The main purpose of this study is to investigate effects of Lu AG06466 on seizure activity after increasing daily doses during 4 weeks in participants with an implanted responsive neurostimulation system.


Clinical Trial Description

This crossover study consists of 2 treatment periods, each of 29 days duration. On Day -1 of treatment period 1, eligible participants will be randomized (1:1) to a sequence of treatments (either Lu AG06466-placebo or placebo-Lu AG06466). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05081518
Study type Interventional
Source H. Lundbeck A/S
Contact
Status Terminated
Phase Phase 1
Start date September 29, 2021
Completion date April 14, 2022

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