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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 Oct 19, 2026, 10:56 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 29, 2024 (Actual)
Primary completion
Aug 31, 2026 (Actual)
Completion
Dec 1, 2026 (Estimated)
Last update posted
Oct 5, 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 Oct 5, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05330182 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →