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Clinical Trial Summary

An open-label, Phase I/II study to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of AST-3424 administered as a single agent


Clinical Trial Description

This is an open-label phase I/II clinical study to evaluate the safety, tolerability, MTD/RP2D, pharmacokinetics, preliminary efficacy, and the relationship between AKR1C3 expression and efficacy of AST-3424 monotherapy in advanced solid tumors. The study is divided into phase I and Phase II. The maximum tolerated dose will be explored in phase I. In phase II, participants will be treated with AST-3424 according to the Phase I confirmed dose. Phase II clinical study will first be conducted in hepatocellular carcinoma (HCC). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06239155
Study type Interventional
Source Ascentawits Pharmaceuticals, Ltd
Contact Claire Hao
Phone (0086)13207649065
Email claire.hao@ascentawitspharm.com
Status Recruiting
Phase Phase 1/Phase 2
Start date September 3, 2019
Completion date November 30, 2025

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