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Clinical Trial Summary

This is an open-label, multicenter, parallel-group study in participants with normal renal function, mild, moderate, or severe renal impairment, or end stage renal disease (ESRD) undergoing standard intermittent dialysis. The pharmacokinetics (PK) of the inactive prodrug VNRX-7145, its active parent drug VNRX-5236, and ceftibuten will be evaluated after a single oral dose of ceftibuten/VNRX-7145.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05488678
Study type Interventional
Source Venatorx Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 1
Start date October 12, 2022
Completion date November 21, 2023

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