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Study identifier: NCT05488340 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Urinary Tract Infections  ·  Sponsor: Locus Biosciences

PhasePhase 2
Planned participants318
Who can joinFemale, 18 Years to 75 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Locus Clinical Operations  ·  (919) 495-4510  ·  clinicaloperations@locus-bio.com

Paul Kim  ·  (919) 495-4510  ·  Paul.kim@locus-bio.com

Always discuss trial participation with your own doctor first.

Locations (17)

Research Site 138Fresno, California, United StatesCompleted
Research Site 131Lancaster, California, United StatesRecruiting
Research Site 123Los Angeles, California, United StatesRecruiting
Research Site 125Montebello, California, United StatesCompleted
Research Site 152Murrieta, California, United StatesRecruiting
Research Site 137San Diego, California, United StatesRecruiting
Research Site 126Tustin, California, United StatesRecruiting
Research Site 102Doral, Florida, United StatesRecruiting
Research Site 151Hialeah, Florida, United StatesRecruiting
Research Site 140Jensen Beach, Florida, United StatesCompleted
Research Site 103Miami, Florida, United StatesRecruiting
Research Site 149Miami, Florida, United StatesRecruiting

+ 5 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05488340