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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
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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Cancer Center, Korea
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.