drugset / Trial / NCT05488340

A Study of LBP-EC01 in the Treatment of Acute Uncomplicated UTI Caused by Drug Resistant E. Coli (ELIMINATE Trial)

NCT05488340

Phase 2 Recruiting 318 enrolled Locus Biosciences Parexel · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2 superiority study of LBP-EC01, a recombinant bacteriophage cocktail, with an initial open-label 3-arm pharmacokinetic (PK) lead-in portion of 30 patients to evaluate the optimal dosing regimen to be used in the subsequent 288 patient blinded portion of the study which will be randomized 1:1 comparing LBP-EC01 + antibiotic versus placebo + antibiotic in patients with a history of prior urinary tract infection (UTI) cased by E. coli. All patients will be required to have an active acute uncomplicated UTI at baseline.

Timeline

Start
2022-07-13
Primary completion
2026-06
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject LBP-EC01 Other / unclassified 1e+10 unknown Other
Subject LBP-EC01 Other / unclassified 1e+11 unknown Other
Subject LBP-EC01 Other / unclassified 1e+12 unknown Other
Subject LBP-EC01 Other / unclassified 2e+12 unknown Other
Background Sulfamethoxazole Small molecule 800 mg Oral
Background Trimethoprim Small molecule 160 mg Oral