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Clinical Trial Summary

Single arm study of induction durvalumab (1500 mg IV) for 1 cycle (every 4 weeks), administered prior to starting concurrent definitive chemoradiation, followed by consolidation durvalumab (1500 mg IV every 4 weeks) for up to 12 cycles. The study will include an initial safety run-in portion. Patients in the safety run-in will be monitored through completion of induction durvalumab, chemoradiation, and 2 cycles of consolidation durvalumab for assessment of safety prior to completion of enrollment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04364048
Study type Interventional
Source Hoosier Cancer Research Network
Contact
Status Active, not recruiting
Phase Phase 2
Start date June 18, 2020
Completion date December 31, 2024

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