| Eligibility |
Inclusion Criteria:
1. =18 years of age on the day of signing informed consent, male or female.
2. Voluntarily agree to provide signed informed consent and are willing and able to
comply with all aspects of the protocol.
3. Histologically or cytologically confirmed diagnosis of HCC. Diagnosis of HCC can be
made without a biopsy if radiographic hallmarks of arterial hypervascularity and
venous/ late phase washout are present by either dynamic contrast enhanced MRI or
helical multidetector CT scan using contrast for a lesion > 2 cm, or by both
modalities for a lesion 1~2 cm.
4. Barcelona Clinic Liver Cancer (BCLC) Stage C or BCLC stage B with bilobar involvement
and infiltrative nature that is not amendable for local therapy (BCLC Classification
see Appendix 7, Section 14.7).
5. Stage 1 only: At least first-line standard treatment failure (disease progression
confirmed by imaging) or intolerance with no restriction on the number of prior lines
of systemic treatment.
6. Stage 2 only: Patients must have objective radiographic disease progression or
intolerance (Intolerance is defined as currently discontinued after =28 days of
treatment due to toxicity) after only one prior line of systemic immunotherapy
treatment with an anti-PD-1/ PD-L1 mAb administered either as monotherapy or in
combination with other checkpoint inhibitors or other therapies (Prior locoregional
therapy such as surgery, radiofrequency ablation or trans-arterial chemoembolization
are also allowed but not counted as systemic therapy, provided that progression has
been documented after these therapies, and =4 weeks have elapsed since the last
therapy).
7. Eligible for treatment with Sorafenib, as determined by investigators according to the
Package Insert and clinical judgment.
8. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1 within 7
days prior to the first dose of study intervention.
9. Patients must have at least one measurable lesion according to RECIST 1.1 as
determined by the investigator, and that has not been the target of local or regional
therapy including trans-arterial chemoembolization, intra-arterial chemotherapy,
ethanol, or radiofrequency ablation; a new area of tumor progression within or
adjacent to a previously treated lesion, if clearly measurable by a radiologist, is
acceptable.
10. Stage 2 only: Patients must have at least one target lesion according to mRECIST that
meet all the following criteria:
- The lesion can be classified as a RECIST 1.1 measurable lesion.
- The lesion is suitable for repeat measurement.
- The lesion shows intratumoral arterial enhancement on contrast-enhanced CT or
MRI.
11. Life expectancy in the judgement of the Investigator > 12 weeks.
12. Recovery to = Grade 1 (CTCAE V5.0) from toxicities related to any prior treatments
unless the adverse events are clinically non-significant and/ or stable with or
without supportive therapy, except for alopecia (any grade) and Grade 2 peripheral
neuropathy.
13. Collection of an archived tissue sample will be requested (where available) to support
evaluation of the clinical utility of biomarker assessment in newly obtained vs.
archived tissue samples; however, a subject will not be precluded from participating
in the study if tissue sample is not available for collection or is otherwise
insufficient for analysis.
14. Patients must have adequate organ function as defined below (Specimens must be
collected within 7 days prior to the start of study intervention):
- Child-Pugh Liver Function Class A (see Appendix 6 in Section 14.6)
- AST or ALT = 5.0 × ULN and total bilirubin = 2 × ULN
- Serum albumin = 2.8 g/ dL
- Creatinine Clearance (CrCL) = 40 ml/ min (Cockcroft-Gault formula: CrCL (mL/ min)
= [140-age(year)] × body weight (Kg)/ [72 × Scr (mg/ dl)]{ × 0.85 for female
subjects})
- International normalized ratio (INR) = 2.0 (except for warfarin therapy)
- Hemoglobin = 8.5 g/ dL, absolute neutrophil count > 1000/ mm3, platelet count
= 60 000/ mm3 (no blood transfusion or blood products or granulocyte
colony-stimulating factor within 14 days, corrected with erythropoietin or
darbepoetin a are allowed)
15. Participants with hepatitis B virus (HBV) or hepatitis C virus (HCV) infection will be
allowed if they meet the following criteria:
- HBV-HCC: Resolved HBV infection (as evidenced by detectable HBV surface antibody,
detectable HBV core antibody, undetectable HBV DNA, and undetectable HBV surface
antigen) or chronic HBV infection (as evidenced by detectable HBV surface antigen
or HBV DNA). Subjects with chronic HBV infection must have HBV DNA < 500 IU/ mL
and must be on antiviral therapy. Active or uncontrolled clinically serious HBV
infections are excluded.
- HCV-HCC: Stable or resolved HCV infection (as evidenced by detectable HCV RNA or
antibody).
16. No other prior malignancy is allowed except for the following: adequately treated
basal cell or squamous cell skin cancer, adequately treated Stage I or II cancer from
which the patient is currently in complete remission per investigators' clinical
judgment.
17. Women of child-bearing potential must have a negative urine or serum pregnancy within
3 days prior to receiving the first dose of study medication and must use accepted
highly effective methods of contraception from the time of signing the informed
consent through 6 months after the last dose of study drug. Men treated or enrolled on
this protocol must also agree to use adequate contraception prior to the study, or be
surgically sterile, for the duration of study participation, and for 3 months after
completion of study drug administration. See Appendix 1 for protocol-approved highly
effective methods of contraceptive combinations.
Exclusion Criteria:
1. Pregnant or breastfeeding patients or expecting to conceive or father children within
the projected duration of the study.
2. Fibrolamellar carcinoma or mixed hepatocellular cholangiocarcinoma.
3. Complete occlusion of the major portal vein or vena cava due to HCC (The major portal
vein is defined as the part of portal vein between the union of the splenic and
superior mesenteric veins and the first bifurcation into the left and right vein).
4. Major surgery within 4 weeks prior to the first dose of study intervention.
5. Previous identified allergy or hypersensitivity to components of WGI-0301 similar
drugs or liposomal drugs or related excipients.
6. Previous identified allergy or hypersensitivity to components of Sorafenib or similar
drugs.
7. Stage 2 only: Received prior Sorafenib therapy or any agents targeting AKT-PI3K
pathway.
8. Currently participating and receiving study therapy or has participated in a study of
an investigational agent and received study therapy or used an investigational device
within 4 weeks prior to the first dose of study intervention.
9. Locoregional therapy to liver within 6 weeks prior to the first dose, including but
not limited to TACE, radiotherapy, radiofrequency ablation, microwave (except
palliative radiotherapy for bone pain relief completed at least 2 weeks prior to the
first dose).
10. Patients on concomitant use of strong CYP3A4 inducers (see Appendix 3 in Section 14.3)
within 12 days prior to the first dose of study intervention. Additionally, patient in
use of transporters based on FDA Drug Development and Drug Interactions, Table of
Substrates, Inhibitors, and Inducers, or strong inducers of transporter, P-gp,
including apalutamide, carbamazepine, enzalutamide, mitotane, phenytoin, rifampin, St.
John's wort. Patient in use of strong inhibitors of transporters based on based on FDA
Drug Development and Drug Interactions, Table of Substrates, Inhibitors, and Inducers.
11. Clinically significant abnormalities of glucose metabolism (e.g., Patients with
diabetes mellitus type1 or diabetes mellitus type 2 requiring treatment, or those with
hemoglobin A1c (HbA1c) =8.0%.
12. clinically significant cardiovascular disease including:
- Uncontrolled chronic hypertension defined as systolic > 150 mmHg or diastolic >
90 mmHg on more than one measurement despite optimal therapy (initiation or
adjustment of BP medication prior to study entry is allowed provided that the
average of 3 BP readings prior to enrollment is < 150/ 90 mmHg).
- Hypotension as indicated by systolic blood pressure < 90 mmHg or mean arterial
pressure < 65 mmHg on 2 consecutive measurements at the Screening Visit.
- NYHA class III or IV Congestive heart failure, myocardial infarction or stroke,
unstable angina pectoris, pericardial effusion (excluding trace pericardial
effusion identified by echocardiography) or left ventricular ejection fraction <
45% within 6 months prior to the first dose.
- Primary cardiomyopathy (e.g., dilated cardiomyopathy, hypertrophic
cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, restrictive
cardiomyopathy, indeterminate cardiomyopathy).
- Bradycardia (known history of cardiovascular disease and either physical
examination at rest or electrocardiogram indicating heart rate < 50 bpm), or
screening ECG indicating QTcF = 470 msec, 2 retests at 30-minute intervals were
required for the first abnormal QTcF, and 3 mean values were taken, Or there is
severe arrhythmia requiring further treatment, including but not limited to
ventricular fibrillation, atrial fibrillation, sustained ventricular tachycardia,
second-degree or third-degree atrioventricular block, torsades de pointes, etc.
13. Clinically significant gastrointestinal disorders including:
- Medical history of difficulty swallowing, malabsorption, or other chronic
gastrointestinal disease, or conditions that may hamper compliance and/ or
absorption of the tested products
- Gastrointestinal perforation and/ or fistula intra-abdominal abscess or
intestinal obstruction within 6 months prior to the first dose
- Clinically significant gastric bleeding within 6 months prior to the first dose
(patients may be enrolled if esophageal and gastric varices are present on
imaging, but no bleeding event or inpatient medical intervention occurs within 6
months prior to the first dose)
14. Clinically significant bleeding risks including:
- Known hereditary or acquired bleeding or thrombotic tendencies (e.g., hereditary
hemorrhagic telangiectasia or von Willebrand disease)
- Bleeding symptoms such as hemoptysis (> 1/ 2 teaspoon bright red blood) and
gastrointestinal bleeding within 3 months prior to screening
- Thrombolytic agents within 10 days prior to the first dose
- Receiving anticoagulant therapy (e.g., anticoagulants, antiplatelets) with an
unstable anticoagulant regimen and/ or dosage (except sodium heparin for
maintenance of central venous catheter patency)
15. History of solid organ transplant.
16. Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)
related illness or is receiving systemic steroid therapy or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study intervention.
17. Known active or uncontrolled infection that could interfere with the study.
18. Uncontrolled ascites or pleural effusion requiring repeated drainage (investigator's
judgment).
19. Past or current history of neoplasm other than HCC, except for curatively treated
nonmelanoma skin cancer, in situ carcinoma of the cervix, or other cancer curatively
treated and with no evidence of disease for at least 3 years.
20. Known central nervous system (CNS) or brain metastasis that is either symptomatic or
untreated.
21. History of drug abuse or addiction at the present stage.
22. Subject has any other conditions or reason that, in the opinion of the Investigator,
interferes with the ability of the subject to participate in the trial, places the
subject at undue risk or complicates the interpretation of data.
|
