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Study on effect and safety for combination of immune checkpoint inhibitor and molecular-targeted therapies for liver cancer

Not Applicable
Conditions
unresectable hepatocellular carcinoma
Registration Number
JPRN-UMIN000043639
Lead Sponsor
agoya University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
91
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who wish to be excluded from the study. Patients who are pregnant, lactating, may become pregnant, or intend to become pregnant, or who wish to have a baby. Patients with the following serious complications: 1.Cardiovascular abnormalities such as heart failure, angina pectoris, or arrhythmia that are difficult to control even after treatment. 2. Myocardial infarction within 6 months of onset 3. Renal failure 4. Active infectious disease except for viral hepatitis 5. Active gastrointestinal bleeding 6. Other active cancer requiring treatment 7. Hepatic encephalopathy or severe mental disorder 8. Severe drug allergy 9. Serious autoimmune disease. Other conditions that the physician deems inappropriate for the safe conduct of this study.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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