drugset / Trial / NCT06470763

A Study Evaluating ANV600 Single Agent or in Combination With Pembrolizumab in Participants With Advanced Solid Tumors (EXPAND-1)

NCT06470763 ↗

Phase 1/2 Completed 63 enrolled Anaveon AG Merck Sharp & Dohme LLC · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of study ANV600-001 is to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, immunogenicity and antitumor activity of ANV600 administered as a single agent or in combination with pembrolizumab in adult participants with advanced solid tumors.

Timeline

Start
2024-07-01
Primary completion
2026-06-22
Completion
2026-06-22

Drugs

EvaluationDrugModalityDoseRoute
Subject ANV600 Unknown — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous

Indications