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A Study Evaluating the Safety and Efficacy of HB0028 in Subjects With Advanced Solid Tumors

Cervical Cancer Clinical Trial

Official title:
A Phase I/II Open Label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Efficacy of HB0028 in Patients With Advanced Solid Tumors

Clinical Trial Summary

It is a phase I/II open label, multicenter study to assess the safety, tolerability, pharmacokinetics, and efficacy of HB0028 in patients with advanced solid tumors.

Clinical Trial Description

This is a phase I/II, multicenter, open-label, first-in-human study in patients with advanced solid tumors. During the phase I study, the safety and tolerability of HB0028 will be evaluated in patients with advanced solid tumors. In the phase II study, the safety and efficacy of HB0028 at the RP2D will be evaluated in cohorts of patients with specific solid tumors. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06223308
Study type Interventional
Source Shanghai Huaota Biopharmaceutical Co., Ltd.
Contact Yuan Tang, Bachelor
Phone 021-51320053
Email yuan.tang@huaota.com
Status Recruiting
Phase Phase 1/Phase 2
Start date September 9, 2022
Completion date October 1, 2024
View Details
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