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Terminated Phase 2Phase 3 Interventional

Clonidine HCl MBT vs. Placebo to Prevent Chemoradiotherapy-Induced Severe Oral Mucositis in Oropharyngeal Cancer.

ClinicalTrials.gov ID: NCT04648020

Public ClinicalTrials.gov record NCT04648020. 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 28, 2026, 7:29 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 2b/3, Multicenter, Randomized, Double-blind, Placebo-controlled Study Comparing the Efficacy and Safety of Clonidine Mucoadhesive Buccal Tablet to Placebo to Prevent Chemoradiotherapy-induced Severe Oral Mucositis in Patients With Oropharyngeal Cancer

Brief summary

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

This study is being performed to evaluate the effectiveness of a new drug, clonidine HCl MBT, to prevent the onset of severe oral mucositis (SOM) in patients with oropharyngeal cancer (OPC) who are being treated with chemoradiotherapy. OPC occurs on the back of the tongue or throat and is often treated by the use of chemoradiotherapy, where radiation is localized to these areas. Radiation to the OPC affected tissues causes the release of small proteins called cytokines that cause damage to the area surrounding the tumor including the oral cavity. This damage is characterized by the formation of mucositis which includes redness, pain and ulcers in the mouth and back of the throat. In addition, as more chemoradiation is administered to treat OPC, the inability to eat a solid diet (a Grade 3 mucositis) or to consume anything at all by mouth (a Grade 4 mucositis) occurs in many patients. Collectively, Grade 3 and Grade 4 mucositis is referred to as SOM. It is a frequent, debilitating side effect of chemoradiation in OPC that may cause patients to stop or interrupt their treatment, develop other side effects like the inability to swallow, or require the increased use of pain medications. OPC survivors who have successful treatment of their tumors often develop permanent swallowing, speaking and range of motion issues that may be linked back to the inability to eat and/or drink caused by SOM during their chemoradiotherapy treatment. Clonidine may inhibit the production of cytokines that cause SOM and clonidine HCl mucoadhesive buccal tablet (MBT) has been designed to deliver sustained high levels of clonidine in the oral cavity, potentially decreasing cytokine production and leading to a decrease in the incidence of SOM. Clonidine HCl MBT is a once per day treatment provided as a tablet that a patient may self-administer to the gums, where it sticks tightly to release clonidine over many hours. The primary objective of this Phase 2b/3 study is to evaluate whether clonidine HCl MBT is more effective than placebo MBT in decreasing the incidence of SOM.

Study identification

NCT ID
NCT04648020
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Monopar Therapeutics
Industry
Enrollment
190 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
Feb 11, 2021 (Actual)
Primary completion
May 14, 2023 (Actual)
Completion
May 14, 2023 (Actual)
Last update posted
May 31, 2023

2021 – 2023

United States locations

U.S. sites
48
U.S. states
25
U.S. cities
45
Facility City State ZIP Site status
University of Arkansas for Medical Sciences Little Rock Arkansas 72205 —
Orange Coast Memorial Medical Center Fountain Valley California 92708 —
Long Beach Memorial Medical Center Long Beach California 90806 —
Pomona Valley Hospital Medical Center Pomona California 91767 —
Grand Valley Oncology Grand Junction Colorado 81505 —
Christiana Care Health Services Newark Delaware 19713 —
Boca Raton Regional Hospital Boca Raton Florida 33486 —
Miami Cancer Institute Miami Florida 33176 —
Memorial Healthcare System Pembroke Pines Florida 33028 —
University Cancer & Blood Center Athens Georgia 30607 —
IACT Health (Centricity Research) Columbus Georgia 31904 —
Decatur Memorial Hospital Decatur Illinois 62526 —
Edward Elmhurst Health Elmhurst Illinois 60126 —
NorthShore University Health Systems Evanston Illinois 60201 —
AMITA Health Hinsdale Illinois 60521 —
UnityPoint Health Cedar Rapids Iowa 52403 —
Des Moines Oncology Research Association Des Moines Iowa 50309 —
East Jefferson General Hospital Metairie Louisiana 70006 —
Louisiana State University Health - Shreveport Shreveport Louisiana 71103 —
Willis-Knighton Cancer Center Shreveport Louisiana 71103 —
Greater Baltimore Medical Center Baltimore Maryland 21204 —
Henry Ford Health System Detroit Michigan 48202 —
Cox Medical Centers Springfield Missouri 65807 —
Summit Health Florham Park New Jersey 07932 —
New York Cancer and Blood Specialists New York New York 10028 —
Northwell Health New York New York 11042 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27514 —
Novant Health Cancer Institute Charlotte North Carolina 28204 —
CaroMont Regional Medical Center Gastonia North Carolina 28054 —
Novant Health Cancer Institute - Forsyth Winston-Salem North Carolina 27103 —
Summa Health System Akron Ohio 44304 —
University of Cincinnati Medical Center Cincinnati Ohio 45219 —
Mercy Health Youngstown Ohio 44501 —
Stephenson Cancer Center Oklahoma City Oklahoma 73104 —
Oklahoma Cancer Specialists Tulsa Oklahoma 74146 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
AHN Cancer Institute - Allegheny General Pittsburgh Pennsylvania 15212 —
Mary Hillman Radiation Oncology Center at UPMC Shadyside Pittsburgh Pennsylvania 15232 —
Reading Hospital West Reading Pennsylvania 19611 —
Rhode Island Hospital Providence Rhode Island 02903 —
Charleston Oncology Charleston South Carolina 29406 —
Ballad Health Johnson City Tennessee 37604 —
Hendrick Cancer Center Abilene Texas 79601 —
Eastern Virginia Medical School Norfolk Virginia 23507 —
PeaceHealth Bellingham Washington 98225 —
Providence Regional Cancer Partnership Everett Washington 98201 —
Benaroya Research Institute at Virginia Mason Seattle Washington 98101 —
HSHS St. Vincent Hospital Cancer Centers at HSHS St. Vincent Hospital Green Bay Wisconsin 54301 —

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 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04648020, 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 May 31, 2023 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04648020 live on ClinicalTrials.gov.

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