Clinical Trials Directory

Trials / Completed

CompletedNCT00867607

Safety, Tolerability, and Efficacy of 21 Days Dermal Application of MRX-6 on Mild to Moderate Contact Dermatitis

A Double-blind, Vehicle-controlled Study to Assess the Safety, Tolerability, and Efficacy of Three Weeks of Daily Dermal Application of MRX-6 (2% HyPE) on the Treatment of Mild to Moderate Contact Dermatitis of the Hand and Forearm

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

A Double-blind, Vehicle-controlled Study to Assess the Safety, Tolerability, and Efficacy of Three Weeks of Daily Dermal Application of MRX-6 or steroid on the Treatment of Mild to Moderate Allergic Contact Dermatitis of the Hand and Forearm. Total number of patients: up to 80.

Conditions

Interventions

TypeNameDescription
DRUGMRX-6b.i.d treatment for 21 days
DRUGSteroidb.i.d. 21 days

Timeline

Start date
2011-03-01
Primary completion
2013-04-01
Completion
2014-03-01
First posted
2009-03-24
Last updated
2015-04-21

Locations

2 sites across 1 country: Israel

Source: ClinicalTrials.gov record NCT00867607. Inclusion in this directory is not an endorsement.

Safety, Tolerability, and Efficacy of 21 Days Dermal Application of MRX-6 on Mild to Moderate Contact Dermatitis (NCT00867607) · Clinical Trials Directory