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
| Type | Name | Description |
|---|---|---|
| DRUG | MRX-6 | b.i.d treatment for 21 days |
| DRUG | Steroid | b.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.