MedPath

S-CUBE

Phase 3
Conditions
Hepatocellular carcinoma
Registration Number
JPRN-jRCT2080220889
Lead Sponsor
Taiho Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1)Patients who are able to do oral administration
2)Patients who have the history of histologically and cytologically confirmed primary hepatocellular carcinoma.
3)Hepatocellular carcinoma patients who are failure to sorafenib monotherapy.
4)Life expectancy of 60 days or more following the start of treatment
5)Patients with written informed consent.

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Overall Survival
Secondary Outcome Measures
NameTimeMethod
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