drugset / Trial / NCT02864082

A Safety and Tolerability Study of Topical PAT-001 in Congenital Ichthyosis

NCT02864082

Phase 2 Completed 19 enrolled Patagonia Pharmaceuticals, LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Congenital ichthyosis (CI) is a large, heterogeneous family of inherited skin disorders of cornification resulting from an abnormality of skin keratinization, such as scaling and thickening of the skin. Treatment options include keratolytic agents, which can abruptly lead to extensive shedding or peeling of scales. PAT-001 primarily acts as a keratolytic agent; thus, making it a potential drug candidate for the treatment of skin disorders associated with hyperkeratinization, such as CI. The current study intends to evaluate the safety and tolerability of PAT-001 in patients with CI of either the Lamellar or X-Linked subtypes.

Timeline

Start
2017-03-08
Primary completion
2018-02-13
Completion
2018-12-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Isotretinoin Other / unclassified 0.1 % Topical
Subject Isotretinoin Other / unclassified 0.2 % Topical

Indications