drugset / Trial / NCT06025344

A Relative Bioavailability Study With a Novel PanCytoVir™ Oral Suspension (100 mg/ml)

NCT06025344

Phase 1 Completed 14 enrolled TrippBio, Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

An open-label, balanced, randomized, two-treatment, two-sequence, two-period, crossover, single dose oral relative bioavailability study of a novel PanCytoVir™ oral suspension (100 mg/mL) versus probenecid 500 mg tablets in normal healthy, adult, human subjects under fasting conditions.

Timeline

Start
2024-09-01
Primary completion
2024-09-30
Completion
2024-10-15

Drugs

EvaluationDrugModalityDoseRoute
Subject PanCytoVir™ Unknown 1000 mg Oral
Subject Probenecid Small molecule 1000 mg Oral

Indications

No indication recorded.