drugset / Trial / NCT05003453

The Effectiveness of a Topical Palmitoylethanolamide (PEA) Formulation (Levagen+) for Reducing Symptoms of Eczema

NCT05003453

Phase 2/3 Completed 72 enrolled RDC Clinical Pty Ltd
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a double blind, randomised, non-clinical study with 2 groups (1 investigational group and 1 comparator group) aiming to assess the effectiveness of PEA for reducing eczema severity compared to a base comparator moisturiser in healthy adults aged over 18 years.

Timeline

Start
2021-11-29
Primary completion
2022-06-03
Completion
2022-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Palmidrol Small molecule 1.5 % Topical

Indications