drugset / Trial / NCT04191148

Safety, Tolerability, and PK of LBP-EC01 in Patients With Lower Urinary Tract Colonization Caused by E. Coli

NCT04191148

Phase 1 Completed 36 enrolled Locus Biosciences
RandomizedParallel-groupTriple-blindBasic science

Summary

Study LBx-1001 is a multi-center randomized, double-blind study to assess the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of LBP-EC01 in patients with indwelling urinary catheters, or requiring intermittent catheterization, and/or patients with asymptomatic bacteriuria caused by Escherichia coli (E. coli). This study population has been selected because LBP-EC01 is a phage cocktail where active bacterial host engagement is required to allow for amplification of the phage and evaluation of the safety and PK of the phage cocktail. Eligible patients will require confirmation of colonization with a urine sample taken within 10 days of randomization that cultures contain ≥10\^3 E. coli colony forming unit (CFU)/mL, without the patient having clinical signs or symptoms of an active urinary tract infection (UTI) requiring antibiotic treatment. Patients should have E. coli as the primary colonizing bacteria and must not have a secondary bacterial colonization at levels equal to or greater than that seen from E. coli.

Timeline

Start
2019-12-30
Primary completion
2020-11-19
Completion
2020-11-19

Drugs

EvaluationDrugModalityDoseRoute
Subject LBP-EC01 Other / unclassified 1.5e+10 unknown Other
Subject LBP-EC01 Other / unclassified 3e+10 unknown Other