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Clinical Trial Summary

The aim of this study is to establish a clinical bridge to Lamisil® tablets by conducting a clinical pharmacokinetic (PK) study comparing the systemic exposure of a Lamisil® tablet with that of with TDT 067 under maximal use conditions.

Under maximal use conditions in onychomycotic subjects, the aim is to confirm that there are significantly lower plasma levels of terbinafine and its major metabolites after a topical administration of TDT 067 for 28 days in comparison with a single oral 250 mg Lamisil® tablet.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01790165
Study type Interventional
Source Celtic Pharma Development Services
Contact
Status Completed
Phase Phase 2
Start date December 2009
Completion date June 2012

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