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Clinical Trial Summary

This study will enroll and treat subjects with cutaneous neurofibromas with NFX-179, a topical study drug. Eligible subjects will receive treatment for 28 days and be observed by a study doctor for approximately 56 days. Subjects will be randomly assigned to 1 of 4 treatment groups. 3 of the treatment groups will receive a specific dose NFX-179, and 1 group will receive placebo. The subject, study doctor, and NFlection Therapeutics will not know what treatment group each subject is assigned. Study participation requires at least 7 clinic visits, blood, urine, and tissue collection, images of the treated cutaneous neurofibromas, electrocardiograms, and information regarding the subject's medical and disease history.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04435665
Study type Interventional
Source NFlection Therapeutics, Inc.
Contact
Status Completed
Phase Phase 2
Start date August 21, 2020
Completion date April 14, 2021

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