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Clinical Trial Summary

This is an open-label, balanced, randomized, two-period, crossover, single dose study to compare the relative bioavailability in normal healthy, adult, human subjects under Fed and Fasting conditions. Subjects will receive a single oral dose of probenecid oral suspension (100 mg/mL) under fed and fasted conditions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06025318
Study type Interventional
Source TrippBio, Inc.
Contact David E. Martin, PharmD
Phone 3015381878
Email davidmartin@trippbio.com
Status Not yet recruiting
Phase Phase 1
Start date June 2024
Completion date October 2024

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