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Active, not recruiting Phase 2Phase 3 Interventional

LMN-201 for Prevention of C. Difficile Infection Recurrence

ClinicalTrials.gov ID: NCT05330182

Public ClinicalTrials.gov record NCT05330182. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 3:11 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-blind, Placebo-controlled Study of LMN-201 for Prevention of C. Difficile Infection Recurrence

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multisite study to evaluate the safety, tolerability, and efficacy of LMN-201 in participants recently diagnosed with CDI who are scheduled to receive or are receiving SOC antibiotic therapy against C. difficile.

Study identification

NCT ID
NCT05330182
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Lumen Bioscience, Inc.
Industry
Enrollment
375 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 28, 2024
Primary completion
Aug 30, 2026
Completion
Nov 30, 2026
Last update posted
Jul 29, 2026

2024 – 2026

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Kaiser Permanente Escondido California 90027
Gastroenterology Center of Connecticut Hamden Connecticut 06518
University of South Florida Tampa Florida 33606
Metro Infectious Disease Consultants, LLC Burr Ridge Illinois 60527
Baptist Health Research Lexington Kentucky 40503
Henry Ford Health System Detroit Michigan 48202
University of Minnesota Minneapolis Minnesota 55455
Mayo Clinic - Rochester Rochester Minnesota 55905
Weill Cornell Medicine New York New York 10021
IMA Clinical Research Mount Airy North Carolina 27030
MD Anderson Cancer Center Houston Texas 77030
Clinical Alliance for Infectious Diseases - Infectious Diseases, LLC Annandale Virginia 22003
University of Virginia School of Medicine Charlottesville Virginia 22903
Kaiser Permanente-Mid Atlantic Springfield Virginia 22015
UW Health University Hospital Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05330182, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 29, 2026 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05330182 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →