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Completed Phase 2 Interventional Results available

A Study to Evaluate LB1148 for Return of Gastrointestinal Function and Adhesions in Subjects Undergoing Bowel Resection

ClinicalTrials.gov ID: NCT02836470

Public ClinicalTrials.gov record NCT02836470. 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 23, 2026, 6:30 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

A Randomized, Double-Blind, Placebo-Controlled Proof of Concept Study to Evaluate LB1148 for Return of Gastrointestinal Function, Post-Operative Ileus and Intra-Abdominal Adhesions in Subjects Undergoing Elective Bowel Resection

Brief summary

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

The purpose of this study is to establish preliminary evidence of the efficacy, safety, and tolerability of LB1148 for the treatment of post-operative ileus and intra-abdominal adhesions in subjects undergoing elective bowel resection.

Study identification

NCT ID
NCT02836470
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Palisade Bio
Industry
Enrollment
112 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Oct 1, 2019 (Actual)
Primary completion
Sep 6, 2023 (Actual)
Completion
Sep 8, 2023 (Actual)
Last update posted
Jun 21, 2024

2019 – 2023

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
Site 315 Mobile Alabama 36617 —
Site 307 Yuma Arizona 85364 —
Site 329 Irvine California 92868 —
Site 310 Pasadena California 91105 —
Site 302 Sylmar California 91342 —
Site 312 Torrance California 90502 —
Site 306 Clearwater Florida 33756 —
Site 303 Miami Florida 33125 —
Site 331 Miami Florida 33126 —
Site 305 Miami Florida 33142 —
Site 308 Orlando Florida 32804 —
Site 328 Louisville Kentucky 40202 —
Site 321 Baltimore Maryland 21237 —
Site 324 Burlington Massachusetts 01850 —
Site 325 Rochester Minnesota 55905 —
Site 317 New York New York 10029 —
Site 323 New York New York 10075 —
Site 318 Chapel Hill North Carolina 27599 —
Site 301 Cleveland Ohio 44195 —
Site 322 Pittsburgh Pennsylvania 15212 —
Site 330 Wynnewood Pennsylvania 19096 —
Site 327 Charleston South Carolina 29425 —
Site 320 Dallas Texas 75390 —
Site 316 Fort Worth Texas 76104 —
Site 311 Houston Texas 77024 —
Site 319 Houston Texas 77030 —
Sie 309 Houston Texas 77089 —
Site 326 Salt Lake City Utah 84132 —

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 NCT02836470, 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 21, 2024 · Synced Oct 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02836470 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →