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Clinical Trial Summary

This study is as an open-label study to be conducted at multiple study centres across New Zealand and Australia designed to characterise the safety, tolerability and preliminary assessment of the anti-tumour efficacy of bacTRL-IL-12 after intravenous (IV) infusion. The study will consist of a screening period (Day -14 to Day -2), treatment and observation (Day 1 to Day 22), safety follow-up period (Day 28 to Day 31), and efficacy follow-up period (until progression, death, revocation of consent, or lost to follow-up).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04025307
Study type Interventional
Source Iqvia Pty Ltd
Contact
Status Terminated
Phase Phase 1
Start date August 5, 2019
Completion date December 29, 2020