drugset / Trial / NCT05830097

A Study of Bi-Ligand-Drug Conjugate CBP-1019 in Patients With Advanced Solid Tumors

NCT05830097

Phase 1/2 Unknown 260 enrolled Coherent Biopharma (Hefei) Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this phase I study is to evaluate the safety and potential efficacy and to determine the recommended phase 2 dose (RP2D) of CBP-1019, a bi-specific ligand conjugated drugs in patients with advanced solid tumors.

Timeline

Start
2023-03-14
Primary completion
2025-06-30
Completion
2025-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject CBP-1019 Other / unclassified Intravenous