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Study of the Effects of Brilacidin Oral Rinse on Radiation-induced Oral Mucositis in Patients With Head and Neck Cancer — Brilacidin  

Head and Neck Neoplasms Clinical Trial

Official title:
Phase 2 Study to Evaluate the Efficacy & Safety of Brilacidin Oral Rinse Administered Daily for 7 Weeks in Attenuating Oral Mucositis in Patients With Head & Neck Cancer Receiving Chemoradiation

Clinical Trial Summary

Oral Mucositis (OM) is a painful and debilitating side effect of many of the drug/radiation regimens used to treat cancer. This study examines the investigational drug brilacidin and its possible application in prevention of oral mucositis in patients undergoing chemoradiation for treatment of head and neck cancer.

Clinical Trial Description

This study will examine whether daily oral rinses with a solution containing brilacidin will prevent the occurrences of OM or lessen the severity of OM if it occurs. Patients will use an oral rinse 3 times daily for up to seven weeks during chemoradiation for head and neck cancer. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02324335
Study type Interventional
Source Innovation Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 2
Start date August 14, 2014
Completion date November 22, 2017
View Details
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