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Brief Title: A Study Evaluating Safety and Therapeutic Activity of ANV419 in Patients With Advanced Cancer.
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
Study ID: NCT04855929
Brief 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.
Detailed 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.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Hospital Vall d'Hebrón, Barcelona, , Spain
START Madrid, Hospital Universitario HM Sanchinarro, Madrid, , Spain
University Hospital Basel, Basel, , Switzerland
Cantonal Hospital St.Gallen, Saint-Gall, , Switzerland
Royal Marsden Hospital, London, , United Kingdom
Name: Eduard Gasal, MD
Affiliation: Anaveon AG
Role: STUDY_DIRECTOR