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Clinical Trial Summary

This is a study to evaluate the maximum tolerated dose (MTD), occurrence of all adverse events (AEs) and serious adverse events (SAEs), pharmacokinetic parameters and antitumor effect of TQB3912 tablets in Chinese adult patients with advanced malignant neoplasm. The study was divided into phase Ia and phase Ib, Phase Ia: Dose escalation period, to evaluate the safety and tolerability of TQB3912 tablets, determine MTD; Phase Ib: Effectiveness exploration period, to expand the safe and effective dose group, and to recommend appropriate dosage and method for subsequent clinical research.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05997342
Study type Interventional
Source Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Contact Qiang Wei, Doctor
Phone +86 028-85422449
Email wq933@hotmail.com
Status Not yet recruiting
Phase Phase 1
Start date August 2023
Completion date August 2025

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