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Completed Phase 3 Interventional Results available

Mesalamine 4 g Sachet for the Induction of Remission in Active, Mild to Moderate Ulcerative Colitis (UC)

ClinicalTrials.gov ID: NCT02522767

Public ClinicalTrials.gov record NCT02522767. 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, 5:06 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 4 g Extended Release Granules (Sachet) for the Induction of Clinical and Endoscopic Remission in Active, Mild to Moderate Ulcerative Colitis

Brief summary

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

The purpose of this trial is to investigate the efficacy of mesalamine for the induction of clinical and endoscopic remission in subjects with active, mild to moderate UC. Subject will receive 4 g extended release granules (sachet) once daily.

Study identification

NCT ID
NCT02522767
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ferring Pharmaceuticals
Industry
Enrollment
228 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
Oct 2015 (Actual)
Primary completion
Feb 6, 2018 (Actual)
Completion
Apr 3, 2018 (Actual)
Last update posted
Mar 15, 2021

2015 – 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 37076 —
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 75 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02522767, 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 Mar 15, 2021 · 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 NCT02522767 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →