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Clinical Trial Summary

This an open label study to assess the pharmacokinetics of CT1812 in normal healthy volunteers.


Clinical Trial Description

Open label study to assess PK in 36 older healthy volunteers. Subjects will be screened 35 days prior dose to determine eligibility. On day -1 subjects will be admitted to the clinical research unit and on day 1 will be randomized to receive one of the following doses: 150 mg BID, 150 mg QD or 300 mg QD in the fed state. Subjects will be confined in the Clinical Research Unit where they will continue to receive study drug and complete safety assessments, PK and CSF draws, until day 16 when they will be discharged. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05248672
Study type Interventional
Source Cognition Therapeutics
Contact
Status Completed
Phase Phase 1
Start date February 15, 2022
Completion date June 1, 2022

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