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Study to Assess the Potential for Adrenal Suppression Following Treatment With DSXS in Patients With Plaque Psoriasis

Plaque Psoriasis Clinical Trial

Official title:
An Open Label, Safety Study to Assess the Potential for Adrenal Suppression Following Maximal Use Treatment With DSXS (Taro Pharmaceuticals U.S.A., Inc.) in Patients With Plaque Psoriasis.

Clinical Trial Summary

An open label, safety study to assess the potential for adrenal suppression following maximal use treatment with DSXS administered twice daily for 28 days in patients with moderate to severe plaque psoriasis.

Clinical Trial Description

1. The objective of this study is to evaluate the potential of DSXS to suppress HPA axis function in patients with moderate to severe plaque psoriasis

2. To evaluate the efficacy parameters, pharmacokinetics and adverse event (AE) profile of DSXS ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02601469
Study type Interventional
Source Taro Pharmaceuticals USA
Contact
Status Completed
Phase Phase 2
Start date September 4, 2015
Completion date August 25, 2017
View Details
See also
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