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A Study Evaluating Safety and Therapeutic Activity of ANV419 in Patients With Advanced Cancer. — ANV419-001  

Lung Cancer Clinical Trial

Official title:
ANV419 First in Human Study Phase 1: Open-label, Dose Escalation Study of ANV419 as Single Agent and in Combination With Ipilimumab in Patients With Relapsed/Refractory Advanced Solid Tumors

Clinical Trial Summary

The purpose of this study is to test the safety and efficacy of ANV419 (single agent) and in combination with ipilimumab in patients with relapsed/refractory advanced solid tumors.

Clinical Trial Description

The purpose of this First-in-Human, open-label, dose escalation study is to assess the initial safety and efficacy profile of ANV419 intravenous infusion alone and in combination with ipilimumab in patients with advanced solid tumours. It will evaluate the safety and tolerability of ANV419 alone and in combination with ipilimumab and, the safest and best dose of ANV419 when used alone or in combination. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04855929
Study type Interventional
Source Anaveon AG
Contact Claudia Schusterbauer, MD
Phone +41615218383
Email anv419-001clinicaltrial@anaveon.com
Status Recruiting
Phase Phase 1
Start date May 25, 2021
Completion date January 2025
View Details
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