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Clinical Trial Summary

The primary purpose of this study is to assess the efficacy of oral TBP-PI-HBr as compared with intravenous (IV) imipenem-cilastatin with respect to the overall response (combined clinical cure plus microbiological eradication) at the Test-of-Cure (TOC) visit in hospitalized adult participants (≥18 years of age) with cUTI or AP.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06059846
Study type Interventional
Source Spero Therapeutics
Contact Caroline Wass
Phone +1 857-242-1555
Email cwass@sperotherapeutics.com
Status Recruiting
Phase Phase 3
Start date December 21, 2023
Completion date December 2025

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