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Clinical Trial Summary

This is a single-arm phase II clinical trial evaluating the safety and efficacy of the PD-L1 inhibitor durvalumab as first-line therapy in 47 patients with advanced NSCLC and ECOG Performance Status 2 (PS2).


Clinical Trial Description

Durvalumab will be supplied in glass vials containing 500 mg of liquid solution at a concentration of 50 mg/mL for intravenous (IV) administration. Durvalumab will be administered at 1500 mg (fixed dose) every 4 weeks until disease progression, death, unacceptable toxicity or withdrawal of consent for a maximum of 12 months of therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02879617
Study type Interventional
Source Academic Thoracic Oncology Medical Investigators Consortium
Contact
Status Completed
Phase Phase 2
Start date April 4, 2017
Completion date June 4, 2022

See also
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