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Study identifier: NCT06348303 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

Study to Assess Drowsiness, Cognition, Fall Risk After Metaxalone 640 mg and Metaxalone 800 mg

Condition: Healthy Participants  ·  Sponsor: Primus Pharmaceuticals

PhasePhase 4
Planned participants20
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

Every participant will receive Metaxalone in two (2) stages, one week after the other. A single dose of each Metaxalone dose will be taken one (1) time after a high fat meal which must be eaten within 30 minutes. Every participant will be given written tests to measure drowsiness, reaction time and thinking process and will also be asked to take walking tests to assess fall risk. Participation in this study will last approximately 2-4 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (1)

ClinOhio Research InstituteColumbus, Ohio, United States

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Source record: clinicaltrials.gov/study/NCT06348303