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Clinical Trial Summary

Open-label, uncontrolled, phase 1-2 study to evaluate the safety, tolerability, pharmacodynamic effects, and preliminary efficacy of ABX196 administered in combination with nivolumab in patients with hepatocellular carcinoma


Clinical Trial Description

This is an open-label, uncontrolled phase 1-2 study to evaluate the safety, tolerability, pharmacodynamic effects, and preliminary efficacy of ABX196 administered in combination with nivolumab in patients with hepatocellular carcinoma. The study consists of 2 phases, a Dose Escalation Phase and an Expansion Phase. Nivolumab will be administered, consistent with the US prescribing information, as a 30-minute IV infusion on Days 1 and 15 of each 28-Day cycle. ABX196 will be administered as an IM injection 120 minutes (+/- 15 minutes) after the completion of the nivolumab infusion on Day 1 of every other 28-Day cycle (i.e., every 8 weeks). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03897543
Study type Interventional
Source Abivax S.A.
Contact Paul GINESTE, PhD
Phone +33 153 830 961
Email paul.gineste@abivax.com
Status Recruiting
Phase Phase 1/Phase 2
Start date August 30, 2019
Completion date June 30, 2023

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