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Clinical Trial Summary

To investigate the efficacy and safety of AK160 in patients with Dupuytren's Contracture.

To determine plasma concentration after the first injection of AK160 in patients with Dupuytren's Contracture.


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 NCT01588353
Study type Interventional
Source Asahi Kasei Pharma Corporation
Contact
Status Completed
Phase Phase 3
Start date May 2012
Completion date January 2014

See also
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