Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:05 PM
Ignite Modification Date:
2025-12-24 @ 3:05 PM
NCT ID:
NCT02965859
Eligibility Criteria:
Inclusion Criteria:
* Are at least 18 years of age and no older than 65;
* Subjects,with an established clinical history of HBV at Screening,has a positive HBsAg test(\>6months) regardless of a positive/negative HBeAg test;
* At Screening,HBV-DNA\>10\^5 copies/ml in HBeAg positive or HBV-DNA\>10\^4 copies/ml in HBeAg negative(HBV-DNA was evaluated by polymerase chain reaction fluorescent labeling.);
* Subjects with abnormal liver function test defined as alanine aminotransferase(ALT) was 2\~10 times upper limit of normal in HBeAg positive or 1.5\~10 times upper limit of normal in HBeAg negative;
* Subjects who are willing to require any other treatment for anti-hepatitis B during the study period;
* Subjects who are willing to take measures for effective non-pharmaceutical contraception;
* Given their signed written informed consent to participate;
Exclusion Criteria:
* Subjects with hepatitis C(HCV),hepatitis D(HDV),autoimmune hepatitis,hereditary liver disease or any other active hepatitis;
* A positive human immunodeficiency virus(HIV) test result;
* Subjects,who in the opinion of the investigator,have a current diagnosis of hepatocellular carcinoma or serum α-fetoprotein(AFP)\>100ug/L;
* Subjects with severe hepatitis or decompensated liver disease defined as hepatic encephalopathy,ascites,low protein blood syndrome(albumin ≤30g/l) or variceal bleeding;
* Serum Creatinine(SCr) exceeds upper limit of normal;
* At Screening,ALT\>10 times upper limit of normal,Total Bilirubin(TBIL)\>double upper limit of normal or transient hepatic decompensation caused by condition aggravation;
* Subjects who required treatment with nucleoside antiviral drugs such as lamivudine,Adefovir dipivoxil,Telbivudine,Tenofovir disoproxil or Entecavir before Screening;
* Subjects who require treatment with interferon-α，thymosin α-1 or other antiviral therapy,immunosuppressive agents,immune modulators within 6 months before Screening;
* Subjects with cardiac disease,hematological system disease,cancer,impaired immunity or psychiatric disease;
* Hemoglobin\<10g/dl,white blood cell count\<3.5 10\^9/L,platelets\<80 10\^9/L;
* Subjects,who in the opinion of the investigator,have a current diagnosis of pancreatitis pre-dose within 24 weeks;
* History of hypersensitivity or allergy to any of the study drugs;
* Subjects who participate in other clinical trials within 3 months prior to Screening;
* Women who are pregnant or lactating or planning a pregnancy recently;
* Subjects in the opinion of the investigator,could not participate in the study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT02965859
Study Brief:
Protocol Section:
NCT02965859