Pilot study to evaluate the next-dose transition from Zolpidem to Lemborexant for treatment of insomnia.

Updated on 23 November 2020


The purpose of this study is to evaluate the next-dose transition from Zolpidem (Ambien) to Lamborexant for treatment of insomnia.



Compensation for time and travel for all completed study visits for qualified participants.

Condition Insomnia
Clinical Study IdentifierTX227885
Last Modified on23 November 2020


Yes No Not Sure

Inclusion Criteria

Currently taking Zolpidem (or other brand), 18 or older, not other sleeping disorder, 7 hours or more in bed each night, and otherwise in general good health
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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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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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