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Clinical Trial Summary

This trial will include:

- Study period up to 7 months.

- Office visits monthly lasting approximately 1 hour.

- Blood Draws.

- Oral medication that is taken 2 times daily.

- Photographs and biopsies if agreed.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00869089
Study type Interventional
Source University Hospital Case Medical Center
Contact
Status Completed
Phase Phase 2
Start date September 2008
Completion date January 2011

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