drugset / Trial / NCT05824663

A Study Evaluating the Safety, Tolerance and Anti-tumor Activity of HBM1020 in Subjects With Advanced Solid Tumors

NCT05824663 ↗

Phase 1 Completed 17 enrolled Harbour BioMed US, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a study to evaluate the safety and tolerability of the study drug HBM1020 which contains two parts. Part 1 will enroll solid tumor participants and Part 2 will enroll renal cell carcinoma (RCC) and colorectal adenocarcinoma (CRC).

Timeline

Start
2023-05-23
Primary completion
2024-10-09
Completion
2024-10-09

Drugs

EvaluationDrugModalityDoseRoute
Subject HBM1020 Monoclonal antibody — Intravenous

Indications