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Clinical Trial Summary

The primary goal of this study is to gather efficacy data concerning the progression-free survival rate with electromagnetic fields plus Regorafenib when compared to historical data with Regorafenib alone as a second-line therapy in patients with advanced hepatocellular carcinoma who have received any first line systemic therapy either standard of care Sorafenib or Lenvatinib or any experimental therapy. Patients who have received any treatment that includes either electromagnetic fields or Regorafenib will be excluded.


Clinical Trial Description

Primary Objective: To estimate progression-free survival rates. Secondary Objectives - To obtain information concerning the feasibility of administration of the proposed treatment, including patient participation in trials using the proposed treatment. - To evaluate safety and tolerability in this patient population. - To evaluate the effect on levels of alpha-fetoprotein. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04327700
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Suspended
Phase Phase 2
Start date January 26, 2021
Completion date November 2025

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