To Evaluate Safety and Efficacy of FB-1603 in Hepatocellular Carcinoma Patient Receiving Transarterial Chemoembolization
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Placebo, FB-1603.
- Who it may be relevant to
- Registry conditions: Hepatocellular Carcinoma. Basic parameters: 18 years — 85 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Taiwan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Phase I/II Randomized, Double-blinded Study of FB-1603 to Evaluate the Safety and Efficacy in Hepatocellular Carcinoma Patients Receiving Transarterial Chemoembolization (FECHT Trial)
Overview
The goal of this clinical trial is to assess the efficacy of FB-1603 on improving liver function impairment in hepatocellular carcinoma patients receiving transarterial chemoembolization. The main question it aims to answer is: Changes in the level of liver function parameters, including AST, ALT, or total bilirubin, from baseline to Visit 3, Visit 4, Visit 5, and Visit 6 There is a comparison group: Researchers will compare arm 1 placebo to see if FB-1603 is work to treat the liver function. Participants will 1. Take drug FB-1603 990mg/day, FB-1603 1980mg/day or a placebo every day for 10 weeks. 2. Visit the clinic on day 4, 7, 10, 14, 28, 56 and 84 (follow-up)
Detailed description
I. Objectives:
* Primary objective: To assess the efficacy of FB-1603 on improving liver function impairment after transarterial chemoembolization (TACE) in subjects * Secondary objective:
* To evaluate the safety of FB-1603 in subjects * To evaluate selected parameters indicative of clinical efficacy * To assess postembolization syndrome improvement of FB-1603 compared with placebo * To evaluate virologic test level of FB-1603 compared with placebo * To assess liver stiffness change of FB-1603 compared with placebo * Exploratory objective:
* To assess the antioxidation activity of FB-1603 in hepatocellular carcinoma (HCC) subjects after TACE
II. Investigational product:
1. Name: FB-1603 oral capsule (FB-1603) 2. Dosage form: 165 mg oral capsule 3. Dose(s): Each arm consisted of 40 subjects.
* Arm 1: 4\*Placebo each time, TID (three times a Day), two weeks before and eight weeks after TACE * Arm 2: 2\*FB-1603 165 mg oral capsule and 2\*Placebo each time, TID (990 mg/day), two weeks before and eight weeks after TACE * Arm 3: 4\*FB-1603 165 mg oral capsule each time, TID (1980 mg/day), two weeks before and eight weeks after TACE 4. Dosing schedule:
All enrolled subjects will be randomly assigned (1:1:1) to receive low dose (990 mg/day), high dose (1980 mg/day) of FB-1603 165 mg oral capsule or placebo capsule three times a day for 10 weeks. Each subject starts receiving FB-1603 165 mg oral capsule or placebo capsule on two weeks before and eight weeks after TACE. The investigational drugs should be taken orally about 10 minutes before the breakfast, lunch, and dinner 5. Mechanism of action:
The proposed mechanism is that FB-1603 can improve liver function via decrease of oxidative stress. In previous study conducted in diethylnitrosamine (DEN) induced liver cirrhosis and cancer rat model (Report #: FENTU30SEP2009) shown that the extent of oxidative stress determined by NBT (Nitro blue tetrazolium) staining was significant decreased in treatment group orally administrated with 0.8, 1 or 2 g/kg/day of FB-1603 compared with the control group.
III. Developmental phase: phase I and II
IV. Study design:
1. placebo control study 2. Blinding: double blind 3. Randomized: yes 4. Parallel 5. Duration of treatment: days 10 weeks months years 6. Titration: forced 7. Single center
VI. Study procedures:
This is a randomized, double-blind, 10-week dose-finding study in 3 parallel arms.
The study is conducted as follows: eligible subjects are randomized parallelly into 3 arms. Each arm comprises 40 subjects orally receive active (FB-1603 165 mg oral capsule) or placebo (placebo capsule) two weeks before and eight weeks after TACE. Each subject will begin receiving FB-1603 oral capsule or placebo two weeks before TACE. As the appearance of the placebo capsule is identical to the FB-1603 165 mg oral capsule, study blinding will be maintained during the administration procedure. Other than staff involved in randomization, the sponsor, participants, and staff involved in the preparation of the study drug are blinded. Each subject is assigned to either active (FB-1603 165 mg oral capsule) or placebo treatment using a block randomization algorithm. Three times a day (TID) doses of FB-1603 165 mg oral capsule are escalated capsule low dose (990 mg/day) and high dose (1980 mg/day).
Interventions
- Drug Placebo
Placebo oral capsule - Drug FB-1603
FB-1603 (165 mg/cap) oral capsule
Primary outcome measures
- Changes in the level of liver function [Time frame: from baseline (day 0) to Visit 3 (day 4), Visit 4(day 7), Visit 5(day 10), and Visit 6(day 14)]
Secondary outcome measures (9)
- Changes in the level of liver function [Time frame: from baseline (day 0) to Visit 7 (day 28) and Visit 8 (day 56)]
- Frequency and severity of adverse event (AE) during the study [Time frame: up to 84 days]
- Clinically significant changes in blood chemistry [Time frame: from baseline (day 0) to Visit 3 (day 4), Visit 4 (day 7), Visit 5 (day 10), Visit 6 (day 14), Visit 7 (day 28), Visit 8 (day 56) and follow-up visit (day 84)]
- Clinically significant changes in coagulation test [Time frame: from baseline (day 0) to Visit 3 (day 4), Visit 4 (day 7), Visit 5 (day 10), Visit 6 (day 14), Visit 7 (day 28), Visit 8 (day 56) and follow-up visit (day 84)]
- Changes in measurements of indocyanine green retention (ICG) [Time frame: from baseline (day 0) to Visit 3 (day 4) and Visit 5 (day 10)]
- Level of liver fibrosis [Time frame: at the screening visit (day -28 to -15), Visit 8 (day 56) and FV/ET (day 84)]
- Incidence of postembolization syndrome [Time frame: from baseline (day 0) to Visit 3 (day 4), Visit 4 (day 7), Visit 5 (day 10), Visit 6 (day 14), Visit 7 (day 28) and Visit 8 (day 56)]
- Length of hospital stay after TACE [Time frame: Visit 2 (day 0)]
- Changes in the level of quantitative HBsAg or HCV RNA [Time frame: from screening visit (day -28 to -15) to Visit 8 (day 56) and FV/ET (day 84)]
Eligibility criteria
Inclusion criteria
- Aged 18-85 years (inclusive) of either gender
- Willing and able to provide signed informed consent
- Confirmed diagnosis of hepatocellular carcinoma by radiology, histology, or cytology
- Subject has the willingness to undergo TACE
- ECOG performance Status of 0-1
- The patient is expected to survive more than 3 months
- Laboratory values should meet all the following standards at the screening visit:
A. AST, ALP and ALT are ≤ 5x ULN. B. International Normalized Ratio (INR) ≤ 1.5 C. Prothrombin time < 4 sec above upper limit of normal D. Absolute neutrophil count ≥ 1.5×10\^9/L; Hemoglobin ≥ 9 g/dL; platelet ≥ 50×10\^9/L.
E. Total bilirubin < 2.5 mg/dL F. Serum creatinine < 2 mg/dL
- With liver stiffness measurement >7 kPa (assessed by FibroScan®) or > 1.5 m/sec (assessed by acoustic radiation force impulse elastography (ARFI))
Exclusion criteria
- Patients with evidence of macrovascular invasion
- Patients with evidence of extrahepatic spread
- Any condition representing a contraindication to TACE as determined by the investigators
- Acute liver failure or liver function decompensation patient perform, such as hepatic encephalopathy, and ascites
- Patients with acute or chronic active hepatitis B or C infection and are recommended to receive HBV or HCV treatment, e.g., Patient with HBV DNA ≥ 20,000 IU/ml or with detectable HCV RNA
- Patients who have severe organic diseases on heart, lungs, brain, kidney, and gastrointestinal tract by the judgment of investigators
- Patients with chronic pancreatitis
- Patients who are taking any prohibited drugs that might interfere the trial
- Patients who are not able to express the chief complaint, for example, the patients with psychosis and severe neurosis
- Patients with active infections (infection requiring the use systemic antibiotics) within 4 weeks prior to the screening visit
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Quadruple blind
- Primary purpose
- Supportive care
Study locations
Taiwan · 2 centers
- National Taiwan University Hospital — Taipei
- Linkou Chang Gung Memorial Hospital — Taoyuan
Identifiers
NCT: NCT06478719 · FB-1603_TACE_PII_2022_1