[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-hepatitis-b-virus-infection\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-hepatitis-b-virus-infection":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100622855","phase-1-a-study-on-ib-001-dose-response-and-tolerability-in-healthy-adults-and-those-with-chronic-hepatitis-b-100622855",false,"NCT07389044","A Study on IB-001 Dose Response and Tolerability in Healthy Adults and Those With Chronic Hepatitis B","A Phase 1, Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate Safety, Tolerability, Pharmacokinetics, And Preliminary Efficacy of Single and Multiple Ascending Doses of IB-001 in Healthy Participants and Participants With Chronic Hepatitis B","PART A: Healthy Volunteers\n\nInclusion Criteria:\n\n1. Able and willing to provide written informed consent.\n2. Male or female aged 18 to 70 years.\n3. Females must not be of childbearing potential OR those who are of childbearing potential must be non-pregnant and non-lactating and willing to use a highly effective method of contraception. Males whose partners are of childbearing potential must either be surgically sterile or willing to use a highly effective acceptable method of contraception.\n4. Non-tattooed, clear injection site suitable for SC injection and monitoring in the opinion of the Investigator.\n\nExclusion Criteria:\n\nHealthy Volunteer participants must not meet any of the following criteria at Screening or upon admission to the site (on Day -1).\n\n1. Major surgery requiring general anesthesia within 12 weeks prior to Screening or is expected to have surgery requiring general anesthesia during the course of the study.\n2. History of severe allergic or anaphylactic reactions, or sensitivity to the IP or its constituents.\n3. Blood donation or blood loss of ≥ 1 unit (450 mL) of whole blood within 4 weeks before Screening or plasma donations within 7 days prior to dosing of investigational product (IP).\n4. Any underlying medical condition (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrinological, tumor, pulmonary, immune, mental, or cardiovascular and cerebrovascular diseases).\n5. History of malignancy, except for non-melanoma skin cancer, excised more than 1 year prior to Screening or cervical intraepithelial neoplasia that has been successfully cured more than 5 years prior to Screening.\n6. Current hepatitis A virus (HAV) infection, hepatitis B virus (HBV) infection, hepatitis C virus (HCV) infection.\n7. Positive test for HIV-1 or HIV-2 antibodies.\n8. Any other active infection requiring systemic antiviral or antimicrobial therapy that will not be completed within 2 weeks of first dosing.\n9. Clinically significant abnormalities on Screening ECG or history of cardiac arrhythmias, risk factors for Torsade de Pointes (hypokalemia, hypomagnesemia, decompensated heart failure and acute myocardial infarction), and a QTcF \\> 450 ms (males) or QTcF \\> 470 ms (females) at Screening.\n10. Physical examination findings at Screening that are considered clinically significant by the Investigator and likely to adversely impact study conduct and\u002For interpretation.\n11. Clinically significant abnormal vital signs\n12. Laboratory abnormalities considered clinically significant by the Investigator at Screening. From Cohort A3 onwards, participants with blood platelet counts \\\u003C 150 × 109\u002FL or absolute neutrophil counts \\\u003C 1.5 × 109\u002FL will be excluded.\n13. Use of any prescribed or over-the-counter medications (including vitamins or herbal remedies) within 2 weeks of first dosing or within 5 times the elimination half-life of the medication prior to first dosing.\n14. Any suspicion or history of drug and\u002For alcohol abuse within the last year.\n15. Pregnant or planning to become pregnant during the course of the study, or currently breastfeeding.\n16. Use of more than 5 cigarettes, or equivalent, a day in the 3 months prior to Screening. Is unwilling to abstain from nicotine-containing products for 48 hours prior to admission to the site and during the in-house stay at the clinical research unit.\n17. Receipt of any investigational drug or product within 90 days of Study Day 1 or within 5 times the elimination half-life of the medication prior to first dosing with the IP, whichever is earlier. Receipt of an invasive medical device within 90 days before first dosing with the IP that in the opinion of the PI or designee may impact the ability of the participant to complete all protocol-required procedures. Participants must not have participated in interventional clinical studies more than 4 times per year.\n18. Use of any prescribed or over-the-counter medications (including vitamins, supplements, or herbal remedies) within 2 weeks of first dosing with the IP or within 5 times the elimination half-life of the medication prior to first dosing with the IP (whichever is longer). Note: Simple analgesia (paracetamol \\\u003C 2 g\u002Fday, nonsteroidal anti-inflammatory drug \\[NSAID\\] at therapeutic doses) may be permitted at the discretion of the PI, and may only be used as premedication prior to dosing of IP if recommended by the SRC.\n19. Has received live vaccine(s) within 28 days of Screening or plans to receive live vaccines within 28 days of dosing with the IP on Study Day 1. Note: COVID-19 vaccines are not considered live vaccines.\n20. Any suspicion or history of drug and\u002For alcohol abuse within the last year.\n21. Positive toxicology Screening panel (urine test including qualitative identification of tetrahydrocannabinol, cocaine, amphetamines, benzodiazepines, opiates, methadone, methamphetamines, ecstasy, and phencyclidine).\n22. Positive alcohol breath test at Screening and\u002For on Study Day -1.\n23. History (within 90 days of Screening) of alcohol consumption exceeding 2 standard drinks per day on average (1 standard drink = 10 grams of alcohol). Alcohol consumption will be prohibited at least 48 hours before dosing with the IP on Study Day 1, and during the in-house stay at the clinical research unit.\n24. Uses more than 5 cigarettes, or equivalent, per day in the 3 months prior to Screening, and\u002For is unwilling to abstain from nicotine-containing products for 48 hours prior to admission to the site and during the in-house stay at the clinical research unit.\n25. Pregnant (positive serum pregnancy test at Screening or a positive urine pregnancy test predose on Study Day -1), planning to become pregnant during the course of the study, or currently breastfeeding.\n26. Any other factor that makes it inappropriate for study participation per the Investigator's judgment.\n\nPART B: Participants with Chronic Hepatitis B (CHB)\n\nInclusion Criteria:\n\n1. Able and willing to provide written informed consent.\n2. Male or female aged 18 to 70 years,\n3. BMI between 18 and 35 kg\u002Fm2.\n4. Females must not be of childbearing potential OR those who are of childbearing potential must be non-pregnant and non-lactating and willing to use a highly effective method of contraception. Males whose partners are of childbearing potential must either be surgically sterile or willing to use a highly effective acceptable method of contraception.\n5. Diagnosed with CHB and are HBeAg-negative (on 2 occasions at least 6 months apart) and have HBsAg titers of ≥ 100 IU\u002FmL at Screening.\n6. Participants must be treatment naive (i.e., have never received treatment with HBV antiviral medicines \\[NUCs, IFN\\] or an investigational anti-HBV agent) or currently not treated (i.e., not been on treatment with approved \\[NUCs, IFN\\] or investigational anti-HBV medicines within 12 months prior to randomization).\n7. Vital signs and physical examination are normal, or abnormal values are not clinically significant in the opinion of the Investigator.\n\nExclusion Criteria:\n\n1. Evidence or history of liver disease of non-HBV etiology, including but not limited to HAV, HCV, HDV, or HEV (endemic regions only) infections; drug- or alcohol-related liver disease; autoimmune hepatitis; hemochromatosis; Wilson's disease; α-1 antitrypsin deficiency; primary biliary cirrhosis; primary sclerosing cholangitis; non-alcoholic steatohepatitis; or any other non-HBV liver disease considered clinically significant by the Investigator. Participants with metabolic dysfunction-associated steatotic liver disease without any signs of steatohepatitis or those with documented Gilbert's Syndrome, are eligible.\n2. Diagnosed or suspected hepatocellular carcinoma (HCC).\n3. Significant liver fibrosis or cirrhosis (FibroScan result \\> 8.5 kPa within 12 months of Screening; Prior liver biopsy with Metavir F3 fibrosis or F4 cirrhosis within 2 years of Screening; AST-to-Platelet Index (APRI) \\> 1 and FibroTest result \\> 0.5 within 12 months of Screening).\n4. Positive for HIV-1 or HIV-2 at Screening.\n5. Active infection requiring systemic antiviral or antimicrobial therapy that will not be completed within 2 weeks of first dosing of investigational product (IP).\n6. Any of the following clinical laboratory values at Screening: ALT or AST ≥ 3 × ULN; blood platelet counts \\\u003C 120 × 109\u002FL; absolute neutrophil count \\\u003C 1.3 × 109\u002FL; hemoglobin \\\u003C 10.0 g\u002FdL; serum total bilirubin ≥ 1 × ULN (Note: for participants with documented Gilbert's Syndrome, total bilirubin ≥ 2 × ULN is acceptable); serum albumin \\\u003C 35 g\u002FL; eGFR of \\\u003C 60 mL\u002Fmin\u002F1.73 m2; INR \\> 1.2 × ULN.\n7. History of severe allergic or anaphylactic reactions, or sensitivity to the IP or constituents.\n8. Blood donation or blood loss of ≥ 1 unit (450 mL) of whole blood within 4 weeks before Screening or plasma donations within 7 days prior to first dosing with the IP.\n9. History or presence of immune-mediated disease (e.g., systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, autoimmune hepatitis, sarcoidosis, psoriasis of greater than mild severity, autoimmune uveitis), or cerebrovascular, chronic pulmonary or cardiac disease associated with functional limitation, retinopathy, uncontrolled thyroid disease (thyroid stimulating hormone \\[TSH\\] \\> 10 or \\\u003C 0.4 mU\u002FL), or uncontrolled seizure disorder, as determined by the Investigator. Participants who are positive for anti-thyroglobulin antibodies or anti-thyroid peroxidase antibodies will be excluded.\n10. History or presence of significant (as judged by the Investigator) cardiovascular, respiratory, renal, gastrointestinal, endocrine, hematological disorders, or diagnosed central or peripheral neurological disease, capable of significantly altering the absorption, metabolism, or elimination of drugs, of constituting a safety-related risk when taking the study treatment, requiring premedication, or of interfering with the interpretation of the data.\n11. Clinically significant 12-lead ECG abnormalities on Screening ECG or history of cardiac arrhythmias, risk factors for Torsade de Pointes (hypokalemia, hypomagnesemia, decompensated heart failure and acute myocardial infarction), and cardiac arrhythmias, risk factors for Torsade de Pointes (hypokalemia, hypomagnesemia, decompensated heart failure and acute myocardial infarction), and QTcF \\> 450 ms for males or QTcF \\> 470 ms for females at Screening.\n12. Physical examination findings that are considered clinically significant by the Investigator and likely to adversely impact study conduct and\u002For interpretation.\n13. Clinically significant abnormal vital signs, confirmed with retesting after at least 5 minutes of additional rest.\n14. History (within 90 days of Screening) of alcohol consumption exceeding 2 standard drinks per day on average (1 standard drink = 10 grams of alcohol).\n15. Positive alcohol breath test at Screening and\u002For on Study Day 1. Alcohol consumption will be prohibited at least 48 hours before each dose with the IP, and during any in-house stays in the clinical research unit or investigational site (if applicable).\n16. Use of more than 5 cigarettes per day or equivalent (e.g., cigarettes, vapes, nicotine patches, cigars, chewing tobacco) in the 3 months prior to Screening. Nicotine-containing products (eg, cigars, cigarettes, vapes) will be prohibited at least 48 hours before each dose with the IP, and during any in-house stays in the clinical research unit or investigational site (if applicable).\n17. Participants must not have participated in interventional clinical studies more than 4 times per year. Receipt of any investigational drug or product within 90-days of Study Day 1 or within 5 times the elimination half-life of the medication prior to first dosing with the IP, whichever is earlier. Receipt of a device within 90 days before first dosing with the IP that in the opinion of the Investigator may impact the ability of the participant to complete all protocol-required procedures or testing.\n18. Received solid organ or bone marrow transplant.\n19. Any immunosuppressing, immunomodulator (e.g., thymosin) or cytotoxic drug administrations within 6 months before first dosing with the IP (Day 1).\n20. Received any antiplatelet (e.g., aspirin, clopidogrel) or antithrombotic therapy (e.g., warfarin, dabigatran, apixaban) within 14 days prior to first dosing with the IP and throughout the study.\n21. Has received live vaccine(s) within 28 days of Screening or plans to receive live vaccines within 28 days of dosing with the IP. Note: COVID-19 vaccines are not considered live vaccines.\n22. Use of corticosteroids above 5 mg\u002Fday of prednisone (or equivalent) or other immunosuppressive medications within 4 weeks prior to Screening. Note: topical, intra-articular and inhaled steroids allowed.\n23. Use of any herbal medicines or supplements within 3 months prior to Screening visit that are known to be hepatotoxic based on Investigator's opinion or who have initiated any new herbal medicine or supplement within 30 days prior to Study Day 1. Eligibility to participate should be discussed with the Sponsor's medical representative.\n24. Pregnant (positive serum pregnancy test at Screening or a positive urine pregnancy test predose on Study Day 1), planning to become pregnant during the course of the study, or currently breastfeeding.\n25. Any other factor that makes it inappropriate for study participation per the Investigator's judgment.\n\nOther prohibited medications during the study: Treatments that may increase ALT or AST (eg, augmentin, \\> 2 g paracetamol\u002Fday, initiating treatment with an HMG-CoA \\[3-hydroxy-3-methylglutaryl coenzyme A\\] reductase inhibitor \\[statins\\]) should be avoided. The use of these drugs, if necessary, should be discussed with the PI or Sponsor's medical representative or designee, preferably before initiation of their administration. Simple analgesia (paracetamol \\\u003C 2 g\u002Fday, NSAID at therapeutic doses) may be prescribed as premedication prior to dosing of IP, if recommended by the SRC.",true,"ALL","18 Years","70 Years",{"count":21,"type":22},80,"ESTIMATED","INTERVENTIONAL",[25],"PHASE1","This study will examine the safety and tolerability of single and multiple doses of IB-001, and will be conducted in two parts:\n\nPart A: SAD study in approximately 50 Healthy Volunteers (HV). Part B: MAD study in approximately 30 adult participants living with Chronic Hepatitis B (CHB).",[28],"Chronic Hepatitis B Virus Infection",[30,31,32,33,34,35],"First in Human","Hepatitis B virus","HBV","Chronic Hepatitis B","Dose finding","Dose Ranging","RECRUITING","2026-06-30",{"date":39,"type":40},"2026-07-02","ACTUAL",{"date":42,"type":40},"2026-02-20",{"date":44,"type":22},"2027-07-01",{"name":46,"class":47},"IntegerBio","INDUSTRY",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":60,"conditions":61,"keywords":62,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100632872","phase-2-clinical-study-to-evaluate-the-efficacy-and-safety-of-hh-006-in-patients-with-chronic-hepatitis-b-virus-infection-100632872","NCT07519330","Clinical Study to Evaluate the Efficacy and Safety of HH-006 in Patients With Chronic Hepatitis B Virus Infection","Phase II Clinical Study to Evaluate the Efficacy and Safety of Multiple Dosing of HH-006 in Patients With Chronic Hepatitis B Virus Infection","Inclusion Criteria:\n\n* Sex: male or female; Age: 18 to 45 years old (inclusive);\n* Male body weight ≥ 50 kg, female body weight ≥ 45 kg, and body mass index (BMI): 18 kg\u002Fm² ≤ BMI ≤ 28 kg\u002Fm²;\n* HBsAg and\u002For HBV DNA positivity for more than 6 months (including 6 months), or previous liver biopsy results indicating chronic hepatitis B, or negative for anti-HBc IgM;\n* Virological and liver function indicators at screening:\n\nCohort 1: HBeAg-positive, 2000 IU\u002FmL ≤ HBsAg ≤ 100,000 IU\u002FmL, HBV DNA \\> 105 IU\u002FmL, 2 × upper limit of normal (ULN) ≤ ALT ≤ 8 × ULN; Cohort 2: HBeAg-negative, 100 IU\u002FmL ≤ HBsAg ≤ 3000 IU\u002FmL, 20 IU\u002FmL \\\u003C HBV DNA ≤ 2000 IU\u002FmL, ALT ≤ 5 × ULN; Cohort 3: HBeAg-negative, 100 IU\u002FmL ≤ HBsAg ≤ 3000 IU\u002FmL, HBV DNA ≤ 100 IU\u002FmL, ALT ≤ 2 × ULN;\n\n* Previous antiviral treatment:\n\nCohort 1 and Cohort 2: No interferon antiviral treatment within the past 1 year, and no nucleos(t)ide analogue (NA) treatment within the 6 months prior to screening; Cohort 3: No interferon antiviral treatment within the past 1 year; received only nucleos(t)ide analogue monotherapy for at least one year;\n\n* Fully understand the study content, procedures, and possible adverse reactions, and sign the written informed consent form (ICF);\n* Able to communicate effectively with the investigator and complete the study in accordance with the study requirements;\n* Male subjects who have not undergone sterilization and female subjects who have been postmenopausal for less than two years must agree to take adequate and effective contraceptive measure from screening until the last follow-up visit.\n\nExclusion Criteria:\n\n* Co-infected with hepatitis C, syphilis, or human immunodeficiency virus (HIV);\n* At screening: total bilirubin ≥ 3 × ULN and direct bilirubin (DBil) \\> 1 × ULN; hemoglobin \\\u003C 100 g\u002FL; platelet count \\\u003C 100,000\u002Fmm³ (100 × 109\u002FL); absolute neutrophil count \\\u003C 1,500\u002Fmm³ (1.5 × 109\u002FL); serum albumin \\\u003C 35 g\u002FL; prothrombin time international normalized ratio (INR) \\> 1.3; glycated hemoglobin (HbA1c) ≥ 7%; estimated glomerular filtration rate (eGFR) (MDRD formula) \\\u003C 60 mL\u002Fmin\u002F1.73 m² (Appendix 2 MDRD calculation formula);\n* Clinically significant electrocardiogram (ECG) abnormalities (e.g., QTcF \\> 450 ms in males, \\> 470 ms in females, severe arrhythmias such as torsade de pointes, paroxysmal ventricular tachycardia, symptomatic atrial fibrillation\u002Fflutter requiring emergency treatment, complete atrioventricular block); poorly controlled or refractory hypertension (e.g., systolic blood pressure ≥ 160 mmHg and\u002For diastolic blood pressure ≥ 100 mmHg after medication use, etc.);\n* Concurrent clinically significant other liver diseases, including but not limited to: moderate or severe fatty liver, alcoholic liver disease, autoimmune liver disease, hereditary metabolic liver disease, drug-induced liver injury, etc.;\n* History of progressive hepatic fibrosis or cirrhosis at any time prior to or during screening;\n* Current or prior history of hepatic decompensation manifestations, including but not limited to: ascites, hepatic encephalopathy, esophageal and gastric variceal bleeding, hepatorenal syndrome, etc.;\n* Previous history of hepatocellular carcinoma, or at screening: serum alpha-fetoprotein (AFP) ≥ 50 ng\u002FmL; or liver ultrasound, computed tomography (CT), or magnetic resonance imaging (MRI) findings suggestive of possible hepatocellular carcinoma;\n* Concurrent severe diseases or clinical conditions in other systems that, in the investigator's judgment, make the participant unsuitable for inclusion in this study:\n\n  1. Circulatory system diseases: e.g., unstable angina, myocardial infarction, congestive heart failure, etc.;\n  2. Respiratory system diseases: e.g., severe chronic obstructive pulmonary disease, etc.;\n  3. Primary or secondary kidney diseases (e.g., chronic renal decompensation, renal diseases secondary to diabetes, hypertension, vascular diseases, etc.);\n  4. Endocrine system diseases: e.g., poorly controlled diabetes or thyroid diseases, etc.;\n  5. Autoimmune diseases: e.g., systemic lupus erythematosus, primary immune thrombocytopenia, rheumatoid arthritis, inflammatory bowel disease, sarcoidosis, autoimmune hemolytic anemia, severe psoriasis, etc.;\n  6. Neuropsychiatric disorders: e.g., epilepsy, schizophrenia, depression, etc.;\n  7. Malignant tumors;\n* Lactating women or those with a positive pregnancy test;\n* Persistent alcohol consumption (average daily intake \\> 40 g alcohol for males, \\> 20 g alcohol for females) or illicit drug abuse within 6 months prior to screening (including the screening period);\n* Participation in any clinical trial of a drug (except for those who did not receive the investigational product) or medical device (except for non-invasive medical devices) within 3 months prior to screening;\n* Major trauma or major surgery within the past three months;\n* History of allergy to HH-003, HH-006, or polysorbate 80;\n* In the investigator's judgment, unsuitability for participation in this study, or close relationship with the study site: e.g., immediate family members of the investigator, or affiliated personnel (e.g., site staff or students).","45 Years",{"count":57,"type":22},45,[59],"PHASE2","Study HH006-202 is designed to assesses the efficacy and safety of HH-006 in adults chronic HBV infection. Eligible participants will receive study treatment for 48 weeks. All treated patients will also undergo a follow-up period after last study drug treatment.",[28],[63],"chronic hepatitis B virus infection","2026-06-11",{"date":66,"type":40},"2026-06-15",{"date":68,"type":40},"2026-05-14",{"date":70,"type":22},"2028-03-22",{"name":72,"class":47},"Huahui Health",1]