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Clinical Trial Summary

The primary purpose of this study is to find the recommended dose of LGK974 as a single agent and in combination with PDR001 that can be safely given to adult patients with selected solid malignancies that have progressed despite standard therapy or for which no effective standard therapy exists


Clinical Trial Description

This open-label multicenter phase 1 dose escalation study will be the first to administer LGK974 as a single agent or in combination with PDR001 in humans. The study will comprise of 2 parts: a dose escalation of LGK974 as a single agent, followed by a safety expansion in specific disease indications; and a dose escalation of LGK974 in combination with PDR001, followed by a safety expansion in cutaneous melanoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01351103
Study type Interventional
Source Novartis
Contact
Status Active, not recruiting
Phase Phase 1
Start date December 1, 2011
Completion date June 18, 2024

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