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Clinical Trial Summary

The primary purpose for this multi-center, non-interventional study is to evaluate the duration of response defined as duration from first documented response of complete response (CR) or partial response (PR) until disease progression (as determined by the treating physician) for participants with laBCC.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02674009
Study type Observational
Source Hoffmann-La Roche
Contact
Status Completed
Phase
Start date September 17, 2015
Completion date March 31, 2019

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