Overview

Exploratory Study of Norepinephrine to Prevent Radiodermatitis in Breast Cancer Patients

Status:
Terminated
Trial end date:
2013-04-01
Target enrollment:
Participant gender:
Summary
This study, a nonrandomized open-label Phase I safety and exploratory study, will evaluate the safety of topical norepinephrine in post-surgical breast cancer patients who are undergoing radiation therapy. The study will also provide information about whether topical norepinephrine can prevent or decrease the severity of the radiation dermatitis experienced by these patients.
Phase:
Phase 1
Details
Lead Sponsor:
ProCertus BioPharm, Inc
Collaborator:
University of Wisconsin, Madison
Treatments:
Norepinephrine