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Clinical Trial Summary

To evaluate safety and the effect of isolated limb perfusion together with nivolumab as a way to increase efficacy and give further insights in early immunological mechanisms. In the first phase Ib part, 20 patients will be enrolled and followed for a minimum of 3 months. An independent data safety monitoring board (DSMB) will continuously review safety and judge the seriousness of the events and also recommend the study to stop if necessary. If the DSMB do not find safety issues, the trial will continue as a phase II trial.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03685890
Study type Interventional
Source Vastra Gotaland Region
Contact Roger Olofsson Bagge, MD, PhD
Phone +46 31 3428207
Email roger.olofsson.bagge@gu.se
Status Recruiting
Phase Phase 1/Phase 2
Start date April 1, 2019
Completion date December 31, 2029

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