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Clinical Trial Summary

A Phase 2 study to investigate the efficacy and safety of lerapolturev alone or in combination with a programmed death receptor-1 (anti-PD-1) inhibitor.


Clinical Trial Description

This multi-center, open-label, randomized, Phase 2 will investigate the efficacy and safety of lerapolturev alone (Arm 1) or in combination with an anti-PD-1 inhibitor (Arm 2). Following a 6 participant safety run-in period, up to approximately 50 participants with cutaneous melanoma who previously failed anti-PD-1/L1-based therapy will be randomized 1:1 to receive either lerapolturev or lerapolturev plus an anti-PD-1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04577807
Study type Interventional
Source Istari Oncology, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date November 17, 2020
Completion date October 2024

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