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Clinical Trial Summary

To determine the Objective Response Rate (ORR) of immunotherapy with Nivolumab (Group 1) and Nivolumab plus Relatlimab (Group 2) in patients with locally advanced/metastatic squamous cell carcinoma of the skin using Response Criteria in Solid Tumors Version 1.1 (RECIST1.1) per site assessment (Time Frame Group 2: From first dose up to 5 years)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04204837
Study type Interventional
Source Salzburger Landeskliniken
Contact Martin Laimer, MD
Phone +4357255
Email m.laimer@salk.at
Status Recruiting
Phase Phase 2
Start date March 6, 2017
Completion date December 2027

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