drugset / Trial / NCT06819735

Study of DT-7012 as a Single Agent and in Combination With an Immune Checkpoint Inhibitor in Participants With Advanced Solid Tumors

NCT06819735 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

This is a phase 1/2, dose-escalation, clinical study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of DT-7012 (an anti-CCR8 monoclonal antibody) as a single agent and in combination with an immune checkpoint inhibitor in adult participants with selected advanced solid tumors.

Timeline

Start
2025-06-25
Primary completion
2027-09
Completion
2028-01

Drugs

EvaluationDrugModalityDoseRoute
Subject DT-7012 Monoclonal antibody — Intravenous

Indications