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Clinical Trial Summary

This study is single-arm, none randomized, open label, two-dose-cohorts, single center clinical trial for evaluation of the safety and efficacy of Oshadi D and Oshadi R in patients with BCC. Patients will receive Oshadi D and Oshadi R for 60 -90 days until the planned surgical excision of the lesion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02007317
Study type Interventional
Source Oshadi Drug Administration
Contact
Status Completed
Phase Phase 2
Start date November 2013
Completion date March 2017

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