The Efficacy and Safety of 12-week SOF/VEL Regimen Combined With Prophylactic Use of TAF for Treatment-naïve Genotype 1-6 HCV/HBV Co-infection Adult Patients With or Without Compensated Cirrhosis in China

Inclusion Criteria:

1. Willing and able to provide written informed consent
2. Male or female, age≥18 years
3. Bodyweight≥40 kg
4. HCV RNA positive (15 IU/mL )at Screening
5. HCV genotype 1, 2, 3, 4, 5, 6, or indeterminate as assessed at Screening by theCentral Laboratory
6. Chronic HBV/HCV coinfection (≥ 6 months) documented by prior medical history or liverbiopsy. For non-cirrhotic patients, and for HBeAg positive patients, HBVDNA<20000IU/ml. For HBeAg negative patients, HBV DNA<2000IU/ml. For cirrhosis patients, HBV DNA was dectable or undectable. Cirrhosis Determination (approximately 20% of subjects may have cirrhosis)

• Cirrhosis by B Ultrasound/CT/ MRI.
• Cirrhosis is defined as Fibroscan® with a result of ≥ 17.5 kPa
• Absence of cirrhosis is defined as Fibroscan with a result of <10.6 kPa within ≤ 6 months of Day 1

7. Classification as treatment naïve for CHC patients Treatment naïve is defined ashaving never been exposed to approved or experimental HCV-specific direct-actingantiviral agents or prior treatment of HCV with interferon or ribavirin
8. Individuals must not be taking or requiring treatment with HBV antiviral therapy atscreening. For participants that are HBV treatment experienced, the most recenttreatment must have been completed at least 6 months prior to Day 1.
9. Patients with HBsAg positive as least 6 month without decompensated cirrhosis.
10. Liver imaging within 6 months of Day 1 is required in cirrhotic patients only toexclude hepatocellular carcinoma (HCC)
11. Females of childbearing potential (as defined in Appendix 4) must have a negativeserum pregnancy test at Screening and a negative urine pregnancy test on Day 1 priorto enrollment
12. Male subjects and female subjects of childbearing potential who engage inheterosexualinter course must agree to use protocol specified method(s) ofcontraception as described in Appendix 4
13. Lactating females must agree to discontinue nursing before the study drug isadministered
14. Subject must be of generally good health, with the exception of chronic HBV/HCVinfection, as determined by the Investigator
15. Subject must be able to comply with the dosing instructions for study drugadministration and able to complete the study -

Exclusion Criteria: 1. Any direct antiviral drugs (DAAs) used before screening, including non-structuralproteins NS3/4A inhibitor, NS5A inhibitor or NS5B polymerase inhibitor. 2. Patients who received hepatitis B antiviral therapy within 6 months. 3. Diagnosis of primary liver cancer or support for the following evidence:alpha-fetoprotein (AFP) >100 ng/ml or cirrhosis imaging studies of the liver revealedsuspicious nodules in the liver 4. A history of malignant tumors within 5 years prior to screening, except for specificcancers that have been cured by surgical resection (eg.Basal cell skin cancer, etc.),or patients suspected of having malignant tumors 5. Current or previous evidence of liver decompensation, including but not limited to:Child-Pugh score Grade B or C, ascites, or hepatic encephalopathy, variceal bleedingor diuretics for the treatment of ascites. 6. A current or previous history of a major medical condition or any other major medicaldisorder that may interfere with the individual's treatment, assessment or complianceprogram. 1. Clinically significant disease (except HBV, HCV) or any other major disease thatmay interfere with subject treatment, assessment, or protocol compliance;subjects that are currently undergoing assessment of a potentially clinicallysignificant disease (except HBV，HCV) are also excluded. 2. Gastrointestinal disease, or the condition after surgery may interfere with theabsorption of the study drug. 3. Difficulty in collecting blood and/or poor venous access for blood collection. 4. Solid organ transplantation. 5. Severe lung disease, severe heart disease or porphyria. 6. Psychiatric hospitalization, attempted suicide and/or a period of disability dueto mental illness in the past 5 years. Subjects with psychiatric illness (withoutpreviously mentioned conditions) who are well-controlled or who have not neededmedication for the past 12 months before Day 1 may Will be included in the study. 7. Serious drug allergies (such as allergic reactions or hepatotoxicity). 7. Pregnant or lactating women. 8. HIV or HDV infection. 9. Screening ECG for clinically significant abnormalities 10. Subjects have the following laboratory test parameters at screening: 1. ALT > 10 Upper Limit of Normal (ULN) 2. AST > 10 ULN 3. Direct bilirubin > 1.5 ULN 4. platelets < 50,000/L 5. HbA1c > 8.5% 6. eGFR < 30 mL/min/1.73 m2，estimated glomerular filtration rate (eGFR) using theCockcroft-Gault equation，eGFR will be calculated by the Cockcroft-Gault method:eGFRCG (mL/min) = [(140 - age (yrs))× weight (kg) × (0.85 if female)] / (serumcreatinine (mg/dL) × 72), where weight is total body mass in kilograms. 7. Female subjects with hemoglobin < 11 g/dL; male subjects with hemoglobin < 12g/dL 8. albumin < 3 g/dL 9. INR > 1.5 x ULN unless the subject has known hemophilia or remains stable foranticoagulant therapy affecting INR 11. Chronic liver disease other than HCV pathogens (eg hemochromatosis, Wilson's disease,alpha-1 antitrypsin deficiency, cholangitis). 12. Known hypersensitivity to SOF/VEL, TAF and RBV (only for GT 3 cirrhosis patients).