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Clinical Trial Summary

To determine the recommended phase 2 dose (RP2D) of the combination of neratinib and sodium valproate when given to patients with advanced solid tumors. Then to explore the antitumor effects of the neratinib and sodium valproate combination in advanced solid tumors with attention to RAS-mutated tumors, EGFR-altered GBM, and ocular melanoma, as part of the phase 2 expansion cohort.


Clinical Trial Description

The purpose of this trial is to test the safety of combining 2 drugs, neratinib (Nerlynx) and divalproex sodium (Depakote DR), also commonly called valproate, when treating patients with advanced cancer. In an earlier stage of this trial the purpose was to test different doses of neratinib in combination with divalproex sodium to see which doses should be used in future research trials. This trial will also help us to learn how advanced tumors respond to the combination of neratinib and divalproex sodium. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03919292
Study type Interventional
Source Virginia Commonwealth University
Contact massey SIIT Team
Phone 804-628-9238
Email masseysiit@vcu.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date May 1, 2019
Completion date December 31, 2025

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