drugset / Trial / NCT02960997

Using Topical Sirolimus 2% for Patients With Epidermolysis Bullous Simplex (EBS) Study

NCT02960997 ↗

Phase 2 Completed 8 enrolled Stanford University
RandomizedCrossoverTriple-blindTreatment

Summary

Epidermolysis bullosa (EB) simplex is a rare orphan disease caused by a mutation in DNA leading to abnormal dominant keratins in the skin. Patients with EB simplex develop lifelong painful thick soles on their feet, and current standard of care is supportive. This pilot study will target the dominant mutant keratin proteins in the skin to ameliorate the severity of EB simplex. The purpose is to improve the function of EB simplex feet with an application of topical sirolimus, 2%. The investigators plan on inhibiting the mTOR pathway to down regulate the translation of defective keratin proteins and work through anti proliferative pathways.

Timeline

Start
2016-05
Primary completion
2018-12-14
Completion
2021-12-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirolimus Small molecule 2 % Topical