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.
Primary Objective: To estimate progression-free survival rates.
Secondary Objectives
| Condition | Hepatocellular Carcinoma |
|---|---|
| Treatment | Regorafenib, TheraBionic |
| Clinical Study Identifier | NCT04327700 |
| Sponsor | Wake Forest University Health Sciences |
| Last Modified on | 18 August 2023 |
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