drugset / Trial / NCT06304571

A Study of HC006 in Subjects With Advanced Solid Tumors

NCT06304571

Phase 1 Recruiting 76 enrolled HC Biopharma Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to characterize the safety, tolerability, pharmacokinetics (PK), Immunogenicity and preliminary antitumor activity of HC006 in subjects with advanced solid tumor malignancies. This study is a first-in-human (FIH) study of HC006 in subjects with advanced solid tumors.

Timeline

Start
2024-02-27
Primary completion
2026-03-15
Completion
2026-07-16

Drugs

EvaluationDrugModalityDoseRoute
Subject HC006 Monoclonal antibody

Indications