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Clinical Trial Summary

The primary purpose of this study is to investigate the efficacy and safety of oral antimycobacterial therapy in patients with confirmed progressive pulmonary sarcoidosis. We suspect that the CLEAR regimen will improve the absolute FVC percent predicted in chronic pulmonary sarcoidosis participants.


Clinical Trial Description

Primary Objective: To assess the efficacy and safety of oral CLEAR therapy in patients with confirmed progressive pulmonary sarcoidosis.

Hypothesis: The CLEAR regimen will improve the absolute FVC percent predicted in chronic pulmonary sarcoidosis participants by augmenting T cell responses through the normalization of p56Lck expression and IL-2 production. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02024555
Study type Interventional
Source Vanderbilt University Medical Center
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Status Completed
Phase Phase 2
Start date March 2014
Completion date April 1, 2019