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Completed Phase 3 Interventional Results available

Mesalamine 2 g Sachet for the Maintenance of Clinical and Endoscopic Remission in Ulcerative Colitis (UC)

ClinicalTrials.gov ID: NCT02522780

Public ClinicalTrials.gov record NCT02522780. 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 6, 2026, 2:13 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 Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Investigating the Efficacy and Safety of Mesalamine 2 g Extended Release Granules (Sachet) for Maintenance of Clinical and Endoscopic Remission in Ulcerative Colitis

Brief summary

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

The purpose of this trial was to investigate the safety and efficacy of mesalamine 2 g extended release granules (sachet) once a day (QD) for maintenance of clinical and endoscopic remission in subjects with UC. The duration of treatment for each subject was 6 months.

Study identification

NCT ID
NCT02522780
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
276 participants

Conditions and interventions

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
Jan 31, 2016
Primary completion
Sep 18, 2018
Completion
Sep 18, 2018
Last update posted
Nov 7, 2021

2016 – 2018

United States locations

U.S. sites
18
U.S. states
9
U.S. cities
17
Facility City State ZIP Site status
Preferred Research Partners Little Rock Arkansas
United Research Institute Murrieta California
Research Associates of South Florida, LLC Miami Florida
IMIC Palmetto Bay Florida
Medical Research Center of Florida Pembroke Pines Florida
Lenus Research and Medical Group Sweetwater Florida
Clinical Trials of SWLA, LLC Lake Charles Louisiana
Cumberland Research Associates, LLC Fayetteville North Carolina
Wilmington Gastroenterology Associates Wilmington North Carolina
Associates in Gastroenterology, PLC Hermitage Tennessee
Quality Medical Research, PLLC Nashville Tennessee
BI Research Center Houston Texas
Biopharma Informatic Inc. Houston Texas
Digestive Health Center Pasadena Texas
DM Clinical Research Tomball Texas
Advanced Research Institute Ogden Utah
New River Valley Research Institute Christiansburg Virginia
Digestive & Liver Disease Specialists Norfolk Virginia

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 78 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02522780, 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 Nov 7, 2021 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02522780 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →