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Clinical Trial Summary

The main purpose of this study was to evaluate the safety and tolerability of CDP1 in patients with advanced solid tumor, to explore dose limited toxicity (DLT), and to determine the recommended dose (RP2D) for phase II clinical trials.


Clinical Trial Description

OBJECTIVES:

Primary:

To evaluate the safety and tolerability of CDP1 in patients with advanced solid tumor, to explore the dose limited toxicity (DLT), and to determine the recommended dose (RP2D) for phase II clinical trial.

Secondary:

To evaluate the pharmacokinetics of CDP1 in patients with advanced solid tumor.

To evaluate the immunogenicity of CDP1 in patients with advanced solid tumor.

To evaluate the initial efficacy of CDP1 in patients with advanced solid tumor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04151810
Study type Interventional
Source Dragonboat Biopharmaceutical Company Limited
Contact Zhang Xiaolei, doctor
Phone (+86)021-50276381
Email zhangxiaolei@dragonboatbio.com
Status Not yet recruiting
Phase Phase 1
Start date December 30, 2019
Completion date June 30, 2021

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