CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 29 enrolled
Drug / intervention
ANV419drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05578872
NCT05578872Phase 2Completed

A Phase 1/2 Study of ANV419 as Monotherapy or in Combination With Anti-PD-1 or Anti-CTLA-4 Antibody Following Anti-PD-1/Anti-PD-L1 Antibody Treatment in Patients With Unresectable or Metastatic Cutaneous Melanoma (OMNIA-1)

Anaveon AG·interventional·Posted Oct 13, 2022·Updated Aug 26, 2025

In Brief

A Phase 2 clinical trial evaluating ANV419 for Melanoma (Skin) and 4 related conditions. Completed, enrolled 29 participants across 25 sites in 5 countries.

Detailed Summary

The purpose of this study is to evaluate the efficacy and safety of ANV419 monotherapy or the combination of ANV419 with anti-PD1 antibody or with anti-CTLA4 antibody in adult participants with advanced (unresectable or metastatic) cutaneous melanoma. The study has 3 parts. Part 1 to evaluate ANV419 in monotherapy and Parts 2 and 3 to evaluate ANV419 in combination with anti-PD1 antibody or anti-CTLA4 antibody. Parts 2 and 3 were not initiated, as the prespecified efficacy criteria to graduate to Part 2 were not met at the interim analysis of Part 1.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Germany, Italy, Spain, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2023202420252026
First PostedOct 13, 2022
Enrollment StartDec 16, 2022
Primary CompletionAug 1, 2024
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 3.7 years ago

Interventions

ANV419drug

ANV419 administered by intravenous (IV) infusion