HCV-positive HCC patients after curative treatment
Conditions
Interventions
investigational material(s)
Generic name etc : NIK-333
INN of investigational material : -
Therapeutic category code : 4-- Agents affecting cellular function
Dosage and Administration for Investigatio
Sponsors
Kowa Company, Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1)Patients with HCV-positive HCC who meet the following conditions before radical treatment 1)Patients diagnosed as having typical HCC on dynamic CT,CTA/CTAP, or dynamic MRI (nodule visualized as a high signal intensity area in the arterial phase and as a relatively low signal intensity area in the portal and equilibrium phases) performed within 8 weeks (56 days) before treatment start prior to radical therapy 2)Patients with the first primary HCC or the first recurrence of primary HCC (2)Patients who received the radical therapies. The treatment duration (from the start to the end of the treatment) should be within 4 weeks (28 days) for each of the radical therapies. (3)Patients showing a complete cure, as confirmed by the dynamic CT images taken from 8 weeks (56 days) to 12 weeks (84 days) after the end of the treatment show a non-stained low-concentration area overlapping the tumor image observed before complete cure. (4)Patients who are able to begin treatment with the study drug within 8 weeks (56 days) after dynamic CT to confirm complete cure (5)Patients confirmed of satisfying the following conditions based on the screening performed at subject registration 1)Positive for serum hepatitis C virus nucleic acid (HCV-RNA) 2)Grade A on Child-Pugh classification 3)Platelet count of 50 000/microL or higher (6)Patients with ECOG Performance Status score of 0 to 1 (7)Patients of the age of 20 years or older at the time of informed consent
Exclusion criteria
Exclusion criteria: (1) Patients positive for HBs antigen (2) Patients showing vascular invasion of HCC on imaging diagnosis (3) Patients who have also undergone transcatheter arterial embolization therapy (TAE/TACE), transarterial infusion therapy (TAI), and chemolipiodolization in combination with the radical therapy (4) Patients who want to receive antiviral therapy such as concomitant therapy with intaferon during the study period (5) Patients who have received other study drugs, anticancer drugs, or interferons after radical therapy (6) Patients who have hypertension as a complication, and whose blood pressure cannot be controlled by drug therapy (systolic blood pressure of 160 mmHg or higher or diastolic blood pressure of 100 mmHg or higher, as determined at subject registration) (7) Patients who have a history of allergy to CT contrast media, and whose participation in this study is judged to be inappropriate by the investigator or the subinvestigator (8) Patients with a history of total gastrectomy (9) Patients with a history of cardiac arrest (10) Patients with any of the following laboratory values or complications 1) Creatinine >= 1.5mg/dL 2) Albumin urine >= 1000mg/g Creatinine 3) Cardiac disorder corresponding to CTC-AE grade 3 in severity 4) HbA1c >= 7.4 under treatment with insulin 5) Autoimmune disease or asthma being treated with oral steroid (11) Patients confirmed of having another malignant neoplasm or who had undergone a radical therapy of HCC within the past 5 years to treat another malignant neoplasm (however, this does not apply to endoscopic resection and resection of intraepithelial carcinoma) (12) Patients who are pregnant, who have a possibility of being pregnant or who have a desire to become pregnant during the study period (13) Lactating women (14) Patients who have a history of allergy to retinoid-related substances (vitamin A, etc.) in the past (15) Patients who participated in another clinical study within past 6 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| efficacy Recurrence-free survival Time to recurrence of HCC or death, regardless of cause | — |
Secondary
| Measure | Time frame |
|---|---|
| efficacy Disease-free survival Time to recurrence of HCC, death, regardless of cause, or occurrence of secondary cancer (malignant tumors other than HCC) efficacy Time to recurrence Time to recurrence of HCC | — |
Countries
Japan
Outcome results
None listed