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Terminated Phase 2 Interventional Results available

Treatment of Septic Shock by Inhibiting Autodigestion and Preserving Gut Integrity With Enteric LB1148

ClinicalTrials.gov ID: NCT02317549

Public ClinicalTrials.gov record NCT02317549. 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 20, 2026, 1:52 PM EDT

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

Official title

Treatment of Septic Shock by Inhibiting Autodigestion and Preserving Gut Integrity With Enteric LB1148 (SSAIL Trial)

Brief summary

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

Septic shock is a potentially life-threatening condition that can result in multi-organ dysfunction syndrome (MODS) and mortality. LB1148 was formulated to preserve gut integrity during physiological shock and ameliorate the subsequent autodigestion leading to MODS and mortality. The purpose of this study in septic shock patients is to determine if enteral administration of LB1148 will increase the number of days alive without cardiovascular, pulmonary or renal replacement therapy through Day 28.

Study identification

NCT ID
NCT02317549
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Leading BioSciences, Inc
Industry
Enrollment
8 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Apr 2015 (Type not available)
Primary completion
Mar 2016 (Actual)
Completion
Mar 2016 (Actual)
Last update posted
Jun 1, 2020

2015 – 2016

United States locations

U.S. sites
26
U.S. states
20
U.S. cities
26
Facility City State ZIP Site status
Providence Hospital Mobile Alabama 36608 —
Community Regional Medical Center, Fresno Fresno California 93721 —
Long Beach Memorial Medical Center Long Beach California 90806 —
UC Davis Medical Center Sacramento California 95817 —
OSF Saint Francis Medical Center Peoria Illinois 61637 —
University of Iowa Iowa City Iowa 52242 —
University of Kansas Medical Center Kansas City Kansas 66160 —
ARH Regional Medical Center Hazard Kentucky 41701 —
University of Louisville Hospital Laboratory Louisville Kentucky 40202 —
Lahey Hospital and Medical Center Burlington Massachusetts 01805 —
Baystate Medical Center Springfield Massachusetts 01199 —
University of Michigan Health Center Ann Arbor Michigan 48109 —
Henry Ford Hospital Detroit Michigan 48202 —
Mayo Clinic Labs - Rochester Campus Rochester Minnesota 55905 —
Barnes Jewish Hospital St Louis Missouri 63110 —
St. Patrick Hospital Missoula Montana 59802 —
Cooper University Hospital Camden New Jersey 08103 —
New York Methodist Hospital Brooklyn New York 11215 —
UNC Chapel Hill Chapel Hill North Carolina 27599 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
Mercy St. Vincent Medical Center, Clinical Research Offices Toledo Ohio 43608 —
OU Medical Center Oklahoma City Oklahoma 73104 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Ben Taub Hospital Houston Texas 77030 —
University of Virginia Health System Charlottesville Virginia 22908 —
Froedtert Hospital and Medial College of Wisconsin Milwaukee Wisconsin 53226 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02317549, 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 Jun 1, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02317549 live on ClinicalTrials.gov.

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