A Phase II Clinical Trial of Hydronidone Capsules(F351) in Patients With Liver Fibrosis Induced by HBV Chronic Hepatitis

Hepatitis B, Chronic Clinical Trial

— HBV  

Official title:

Randomed and Double-blinded Phase II Clinical Trial of Hydronidone Capsules(F351) in Patients With Liver Fibrosis Induced by HBV Chronic Hepatitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02499562
• Other study ID #: GNI-F351-201402
• Status: Completed
• Phase: Phase 2
• Start date: June 25, 2015
• Est. completion date: November 20, 2020

Study information

• Verified date: June 2022
• Source: Shanghai Genomics, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To explore the effective dose and safety of the effect of hydronidone and entecavir on hepatic fibrosis in chronic viral hepatitis B.

Description:

Primary observation indexes: Hepatic fibrosis Ishak score after treatment decreases by the proportion not less than 1 compared with that before treatment. Secondary observation indexes : 1. Negative conversion ratio of HBV DNA after treatment (HBV DNA<1×103copies/mL) and falling range. 2. The falling proportion of Fibrocan Kpa value after treatment compared with that before treatment. 3. The falling proportion that decreases not less than 1 level and progression-free fibrosis after treatment compared with that before treatment. 4. The improvement of ALT of liver function.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 168
• Est. completion date: November 20, 2020
• Est. primary completion date: November 20, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Aged 18-65, all genders.

2. History of chronic hepatitis B, HBsAg positive?six months.

3. ALT<eight-fold ULN (maximum).

4. Significant liver fibrosis confirmed by liver biopsy.

5. HBeAg positive patients, HBV DNA>2.0×104 IU/mL (copies/mL); HBeAg negative patients,HBV DNA>2.0×103 IU/mL (104copies/mL).

6. Having not accepted the antiviral therapy with interferon and/or nucleoside analog.

7. Having not taken anti-inflammatory drugs to protect liver within 1 month before selection.

8. Capable of understanding and signing the informed consent before the study.

Exclusion Criteria:

1. Failing to meet any one requirement of the inclusion criteria.

2. Having suffered massive hemorrhage of gastrointestinal tract within 3 months before selection

3. TBiL>three-fold ULN.

4. AFP>100 ug/L

5. PLT?60×109/L

6. PTA<50%

7. Having obvious space-occupying lesion in liver as shown by B ultrasound examination.

8. With a portal vein ?1.2cm wide as shown by B ultrasound examination.

9. BMI index>30.

10. The patient who suffered from liver function decompensation hepatic cirrhosis and liver neoplasms.

11. The patient with alcoholic, drug-induced, hereditary, immune and other viral and non- viral chronic hepatitis.

12. The patient with angiocarpy, lung, kidney, incretion, nerve and blood system disease and mental disease.

13. The patient with active peptic ulcer.

14. Gestational and breast feeding women.

15. The subject is the legal disabled person according to the Law of the People's Republic of China on the Protection of Disabled Persons of the April 2008 edition.

16. The subject who participated in other drug tests within recent 3 months.

17. The patient who is suspected with poor compliance or disagrees to participate in the test.

18. The patient who is considered by other investigators not to be suitable for participating in the study.

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis A
• Hepatitis B
• Hepatitis B, Chronic
• Liver Cirrhosis

Intervention

Drug:
• Hydronidone
The investigational products in the test groups and control group shall be orally taken 30 minutes before meals for 52 continuous weeks. There are respectively 60 cases in the test group I, II, III and the control group, totally 240 cases.
• Placebo

• Entecavir

Locations

Country	Name	City	State
China	Shanghai General Hospital	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Shanghai Genomics, Inc.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in hepatic fibrosis in chronic viral hepatitis B		one year