NCT05117957CompletedPhase 2
Efficacy and Safety of Sorafenib in Previously Treated Advanced Hepatocellular Carcinoma: SOPT Study
Source: ClinicalTrials.gov · Last updated 24 Jul 2026
Brief summary (registry, in English)
To investigate the efficacy and safety of sorafenib administered as later lines of treatment in patients with advanced HCC.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 50 (actual)
- First submitted
- 21 Oct 2021
- Start date
- 8 Mar 2022
- Primary completion date
- 30 Jun 2025
- Lead sponsor
- Bo Hyun Kim
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT05117957
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 50
- From 8 Mar 2022 to the primary completion date, 30 Jun 2025
- 1 site 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.
Other illness
- Presence of active bacterial infection
- Other malignant disease (a history of treated malignancy -other than HCC- is allowable if the patient's malignancy has been in complete remission, off chemotherapy and without additional surgical intervention, during the preceding two years)
Other
- Fibrolamellar carcinoma or sarcomatoid carcinoma
- Having active brain metastasis or leptomeningeal metastasis
- Moderate to severe or intractable ascites
- Presence of hepatic encephalopathy
- Uncontrolled severe medical comorbidity
- Other patients judged by the investigator or sub-investigator to be inappropriate as subjects of this study
Who the study is looking for
- Signed written informed consent
- Age of 20 or more
- Histological or clinical diagnosis of HCC based on the guidelines of the Korean Liver Cancer Association-National Cancer Center
- Locally advanced unresectable or metastatic disease not amenable to curative surgical and/or locoregional therapies
- Intolerant to or progressed on at least 1 prior systemic treatment for HCC
- Having at least one measurable target lesion (per RECIST v1.1)
- \- Patients who received prior local therapy (e.g., radiofrequency ablation, transarterial chemoembolization, transarterial embolization, radiation therapy etc.) are eligible provided that other target lesion(s) have not been previously treated with local therapy or the target lesion(s) within the field of local therapy have subsequently progressed in accordance with RECIST 1.1.
- Child-Pugh class A or B7
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1
- Life expectancy of at least 16 weeks
- Adequate hematologic and hepatic function (should be obtained within 14 days prior to initiation of study treatment):
- Women of childbearing potential and men must agree to use highly efficient contraception since signing of the IC form until at least 5 months (women) and 7 months (men) after the last study drug administration.
Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| National Cancer Center, Korea Coordinator of this site? Confirm its status | Seoul | South Korea | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.