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Hepatitis B virus infection is a worldwide disease and is still the most common cause of hepatocellular carcinoma (HCC).Existing treatments for hepatitis B infection have various side-effects including renal toxicity and drug resistance or failure.
Hepatitis B virus infection is a worldwide disease and is still the most common cause of hepatocellular carcinoma (HCC). Those carriers in China account for 33% of all chronic carriers globally. A big epidemiological study of patients with chronic hepatitis B has revealed that baseline HBV DNA level or cirrhosis is an independent predictor for the occurrence of HCC.
Antroquinonol is a new chemical entity isolated from the mycelium of Antrodia camphorata, which showed interesting anticancer and anti-inflammatory activities.Previous studies have indicated that signaling molecules, such as PI3K, AMPK, and mTOR, participate in Antroquinonol-induced cancer cell death, whereas Nrf2 and NF-kB are involved in the anti-inflammatory effects of Antroquinonol. Moreover, we also found the administration of Antroquinonol also differentially modulated T cell activity and reduced IL-18 production, but enhanced the activation of Nrf2 and, thus, suppressed oxidative stress by animal studies. These results demonstrate the potential applications of Antroquinonol in treating hepatitis B.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Antroquinonol 100 mg PO BID | Experimental | Antroquinonol (Hocena) 50mg/capsule. 2 capsules antroquinonol, twice a day. |
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| Antroquinonol 50 mg PO BID | Experimental | Antroquinonol (Hocena) 50mg/capsule. 1 capsule antroquinonol and 1 capsule placebo,twice a day. |
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| Placebo | Placebo Comparator | Placebo capsule, 2 capsules placebo, twice a day |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Antroquinonol | Drug | Antroquinonol will be provided as a capsule-shaped which contain 50 mg Antroquinonol. |
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| Measure | Description | Time Frame |
|---|---|---|
| Percentage | The percentage improvement between baseline and day 85 in quantitative HBsAg. | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| IU/mL | Sserum hapatitis B virus DNA level | 4 week |
| score | The Fibrosis-4 score helps to estimate the amount of scarring in the liver |
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Inclusion Criteria:
Exclusion Criteria:
Evidence of hepatic decompensation such as:
Abnormal hematological and biochemical parameters at screening A、 White blood cell count less than 2500 cells/uL B、 Absolute neutrophil count (ANC) less than 1,000 cells/mm3 (less than 750 mm3 for African or African-American subjects) C、 Hemoglobin less than 12 g/dL for males, less than 11 g/dL for females D、 Estimated GFR less than 50 mL/min
Suspected or confirmed liver diseases from etiologies other than HBV (such as alcohol, toxin, drug, shock, acute viral hepatitis A or E), co-infection with human immunodeficiency virus, hepatitis C virus or hepatitis delta virus, prior antiviral treatment with NUCs or interferon, and recent immunosuppressive therapy (including chemotherapy and systemic corticosteroid).
Immunodeficiency disorders or severe autoimmune disease
Severe pulmonary disorders or significant cardiac diseases
Gastrointestinal disorder with post-operative condition that could interfere with drug absorption
Significant psychiatric illness that in the judgment of the Investigator, is a contraindication to protocol participation or impairs a volunteer's ability to give informed consent
Any malignancy diagnosed within 5 years or evidence of hepatocellular carcinoma (e.g., α fetoprotein > 50ng/mL or radiologic evidence)
Solid organ transplantation
Current drug or alcohol abuse
Pregnancy or lactation
Under hepatitis B antiviral or interferon treatment within 3 months
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| Name | Affiliation | Role |
|---|---|---|
| Ching-Pin Lin, MD | Chung Shan Medical University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chung Shan Medical University Hospital | Taichung | Taiwan |
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| ID | Term |
|---|---|
| C545357 | antroquinonol |
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This is a single-center, phase IIa, double blind, and randomized, placebo-controlled trial of Antroquinonol in patients with hepatitis B infection. Subjects with diagnosis of hepatitis B meet inclusion/exclusion criteria will be randomized into 3 groups:
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| placebo | Other | The matching placebo will be packaged as Antroquinonol with appearance identical in all aspects |
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| 12 week |
| Unit/L | Glutamic Oxaloacetic Transaminase | 4 week |
| Unit /L | Glutamic Pyruvic Transaminase | 4 week |