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Clinical Trial Summary

This is a phase 1 dose escalation study testing the addition of an anti-IL6 (siltuximab) to standard induction chemotherapy for high-risk AML.


Clinical Trial Description

Administration of siltuximab at day 8 of induction following a classical induction using idarubicin 8mg/m2/d for 5 days and cytarabine 100mg/m2/d for 7 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05697510
Study type Interventional
Source Nantes University Hospital
Contact MARION GAUTIER
Phone +33253526204
Email marion.gautier@chu-nantes.fr
Status Recruiting
Phase Phase 1
Start date March 16, 2023
Completion date June 30, 2025

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