drugset / Trial / NCT06466265

Study of DNP002 in Patients With Solid Tumors

NCT06466265 ↗

Phase 1 Unknown 36 enrolled Kumho HT Inc.
NaSequentialOpen-labelTreatment

Summary

This is an open-label, Phase 1, first-in-human, dose-escalation study designed to assess the safety, tolerability, pharmacokinetics, and preliminary efficacy of the anti-Carcinoembryonic-antigen-related-cell-adhesion-molecule-6 (CEACAM6) antibody DNP002 in patients with advanced solid tumors.

Timeline

Start
2021-05-24
Primary completion
2024-12
Completion
2025-06

Drugs

EvaluationDrugModalityDoseRoute
Subject DNP002 Unknown — Intravenous

Indications

No indication recorded.