NCT07118202Recruiting
TheraBionic P1 Device in Subjects With Advanced Hepatocellular Carcinoma
TheraBionic P1 Device for Patients With Advanced Hepatocellular Carcinoma (HCC) Who Fail First and Second Line Therapy
Source: ClinicalTrials.gov · Last updated 13 Apr 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if the TheraBionic P1 device given to patients with advanced hepatocellular carcinoma (HCC) who have no standard of care options can affect patients survival. The main questions it aims to answer are: * will the TheraBionic P1 device affect overall survival in advance HCC * the long term safety and tolerability of the TheraBionic P1 device * assessment of how the disease responded to the TheraBionic P1 device
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 198 (estimated)
- First submitted
- 5 Aug 2025
- Start date
- 20 Oct 2025
- Primary completion date
- 31 Aug 2028
- Lead sponsor
- Barbara Ann Karmanos Cancer Institute
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT07118202
What you commit to
- Study type: Interventional
- Planned participants: 198
- From 20 Oct 2025 to the primary completion date, 31 Aug 2028
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients taking any other investigational drugs
Other illness
- Patients with known active secondary malignancy, unless, in the opinion of the investigator, it is unlikely to interfere with the safety and efficacy of the endpoints
- Patients with a known severe (e.g., anaphylactic) allergy to nickel
Lab values
- Patients receiving calcium channel blockers and any agent blocking L-type of T-type Voltage Gated Calcium Channels, e.g., amlodipine, nifedipine, ethosuximide, ascorbic acid (vitamin C), etc. unless their medical treatment is discontinued to prior to treatment on study. Patients must agree to abstain from using calcium channel blockers and any agent blocking L-type or T-type voltage gated calcium channels for the duration of treatment on study.
Other
- Patients with active oral mucosal inflammation, ulceration, or other pathology that could interfere with the use of the device
- Patients who are breastfeeding. If a breastfeeding participant would like to be part of this study, breastfeeding must be discontinued.
- Patients that do not agree to be followed according to the study protocol or have cognitive or physical inability to use the device for the prescribed period and frequency (three 60-minute treatments in the morning, middle of the day, and evening)
Who the study is looking for
- Patients with advanced hepatocellular carcinoma (HCC) (defined as a liver tumor not eligible for local therapies given the extent of disease or a livor tumor that recurred after local therapy)
- Patients who have failed at least two lines of therapy\* or who are no longer eligible for any line of standard therapy or who are intolerant to at least two lines of therapy.
- Patients with evaluable disease
- Patients must be ≥ 22 years old and must be able to understand and sign an informed consent.
- Female patients of childbearing potential and their partners and male patients must agree to use adequate contraception during the period of study treatment.
- Patients with a life expectancy of at least 3 months
Age in the registry: 22 years to - · Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Karmanos Cancer Institute at McLaren Bay Region Coordinator of this site? Confirm its status | Bay City | United States | Recruiting |
| Karmanos Cancer Institute Coordinator of this site? Confirm its status | Detroit | United States | Recruiting |
| Karmanos Cancer Institute at McLaren Flint Coordinator of this site? Confirm its status | Flint | United States | Recruiting |
| Karmanos Cancer Institute at McLaren Greater Lansing Coordinator of this site? Confirm its status | Lansing | United States | Recruiting |
| Karmanos Cancer Institute at McLaren Lapeer Region Coordinator of this site? Confirm its status | Lapeer | United States | Recruiting |
| Karmanos Cancer Institute at McLaren Central Michigan, Morey Cancer Center Coordinator of this site? Confirm its status | Mount Pleasant | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.