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Terminated Phase 2 Interventional

Study of the Research Medicine CIN-103 in Adults With Irritable Bowel Syndrome With Predominant Diarrhea (IBS-D).

ClinicalTrials.gov ID: NCT06153420

Public ClinicalTrials.gov record NCT06153420. 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 24, 2026, 6:32 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, Multicenter, Parallel-Group Study to Evaluate the Efficacy, Safety, and Tolerability of CIN-103 in Adults With Irritable Bowel Syndrome With Predominant Diarrhea (IBS-D)

Brief summary

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

The goal of this clinical trial is to evaluate if the study drug, CIN-103, can help reduce the symptoms associated with irritable bowel syndrome with predominant diarrhea (IBS-D) in adult patients. The main questions it aims to answer are: * To evaluate the efficacy of CIN-103 on symptoms of IBS-D when given to patients with IBS-D compared to a placebo. * To evaluate the safety and tolerability of CIN-103 when given to patients with IBS-D compared to a placebo Participants will attend the following visits: * Screening Period (1 Visit) * Baseline Period (1 Visit) * Will complete daily diary and other Patient Reported Outcomes (PROs) as described in the protocol to assess eligibility for continued participation. * 12-Week Treatment Period (5 Visits) * Study drug taken twice daily by mouth. * Will complete daily diaries and other PROs as described in the protocol. * Follow- Up Period (1 Visit) Researchers will compare CIN-103 Dose 1, CIN-103 Dose 2, and placebo, to evaluate the clinical response to multiple dose strengths of CIN-103 relative to placebo on abdominal pain and stool consistency along with safety and tolerability.

Study identification

NCT ID
NCT06153420
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
CinPhloro Pharma, LLC
Industry
Enrollment
421 participants

Conditions and interventions

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
Dec 28, 2023 (Actual)
Primary completion
Jul 28, 2025 (Actual)
Completion
Jul 28, 2025 (Actual)
Last update posted
Dec 15, 2025

2023 – 2025

United States locations

U.S. sites
53
U.S. states
24
U.S. cities
48
Facility City State ZIP Site status
Digestive Health Specialists - Dothan Dothan Alabama 36305 —
Clinical Research Associates, LLC Huntsville Alabama 35801 —
Elite Clinical Studies LLC Phoenix Arizona 85018 —
GI Alliance - Sun City Sun City Arizona 85351 —
Applied Research Center of Arkansas Little Rock Arkansas 72212 —
Paragon Rx Clinical, Inc. - Garden Grove Garden Grove California 92840 —
Gastro Care Institute- lancaster Lancaster California 93534 —
Medical Associates Research Group San Diego California 92123 —
American Family Research Group Cape Coral Florida 33909 —
USA and International Research Inc. Doral Florida 33126 —
International Research Associates LLC Miami Florida 33183 —
Innovation Medical Research Center Palmetto Bay Florida 33157 —
Velocity Clinical Research,, Savannah Savannah Georgia 31406 —
Southwest Gastroenterology Oak Lawn Illinois 60453 —
DelRicht Research Mandeville Louisiana 70471 —
Tandem Clinical Research GI LLC Marrero Louisiana 70072 —
Tandem Clinical Research GI LLC Metairie Louisiana 70006 —
DelRicht Research New Orleans Louisiana 70115 —
Delta Research Partners, LLC West Monroe Louisiana 71291 —
DelRicht Research of Bethesda Clinical Trials Rockville Maryland 20852 —
St. Charles Clinical Research Weldon Spring Missouri 63304 —
Quality Clinical Research, Inc Omaha Nebraska 68114 —
Las Vegas Medical Research Las Vegas Nevada 89113 —
Digestive Disease Specialists Las Vegas Nevada 89128 —
Advanced Research Institute - Reno Reno Nevada 89511 —
Allied Digestive Health Clinical Research Organization Somers Point New Jersey 08244 —
Allied Digestive Health-Jersey Shore Gastroenterology - Point Commons Somers Point New Jersey 08244 —
Albuquerque Clinical Trials, Inc Albuquerque New Mexico 87102 —
Westchester Putnam Gastro Carmel Hamlet New York 10512 —
IMA Clinical Research PC and Affiliates- New York, NY New York New York 10128 —
NY Scientific New York New York 11235 —
Atrium Health - Center for Gastroenterology and Hepatology MMP Charlotte North Carolina 28204 —
Peters Medical Research High Point North Carolina 27262 —
IMA Clinical Research Mount Airy North Carolina 27030 —
Cleveland Clinic Cleveland Ohio 44195 —
Remington Davis, Inc. Columbus Ohio 43215 —
Great Lakes Gastroenterology Research LLC Mentor Ohio 44060 —
Northshore Gastroenterology Research, LLC Westlake Ohio 44145 —
Options Health Research LLC Tulsa Oklahoma 74104 —
Susquehanna Research Group, LLC Harrisburg Pennsylvania 17110 —
DelRicht Research of Charleston Clinical Trials Charleston South Carolina 29407 —
Palmetto Clinical Research Summerville South Carolina 29485 —
Galen Medical Group - Downtown Gastroenterology Location Chattanooga Tennessee 37404 —
Tri-Cities Gastroenterology Kingsport Tennessee 37663 —
Advanced Gastroenterology Union City Tennessee 38261 —
The University of Texas Health Science Center at Houston Bellaire Texas 77401 —
The Clinical Trials Network LLC Houston Texas 77074 —
Care and Cure Clinic Houston Texas 77090 —
GLRI - McAllen Research Pharr Texas 78577 —
Quality Research Inc San Antonio Texas 78209 —
Gastroenterology Research of San Antonio San Antonio Texas 78229 —
Advanced Research Institute Ogden Utah 84405 —
GI Alliance - Washington Gastroenterology Tacoma Washington 98405 —

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 NCT06153420, 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 Dec 15, 2025 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06153420 live on ClinicalTrials.gov.

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