drugset / Trial / NCT04866485

A Study to Evaluate Safety, Tolerability, PK/PD and Preliminary Efficacy of HBM4003 Combined With Anti-PD-1 Antibody

NCT04866485

Phase 1 Unknown 66 enrolled Harbour BioMed (Guangzhou) Co. Ltd.
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multi-center phase 1 study. The trial, consisting of Part 1a dose confirmation and Part 1b dose expansion, is designed to evaluate the safety, tolerability, PK/PD and preliminary efficacy of HBM4003 in combination with pembrolizumab in patients with advanced NSCLC and other solid tumors.

Timeline

Start
2021-06-14
Primary completion
2023-02
Completion
2023-02

Drugs

EvaluationDrugModalityDoseRoute
Subject PORUSTOBART Monoclonal antibody
Background Pembrolizumab Monoclonal antibody

Indications