drugset / Trial / NCT05488340
A Study of LBP-EC01 in the Treatment of Acute Uncomplicated UTI Caused by Drug Resistant E. Coli (ELIMINATE Trial)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |