[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"primary-hyperlipidemia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:primary-hyperlipidemia":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,67],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":4},"100637657","phase-3-a-clinical-study-to-evaluate-the-efficacy-and-safety-of-bempedoic-acid-100637657",false,"NCT07623915","A Clinical Study to Evaluate the Efficacy and Safety of Bempedoic Acid","A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of Bempedoic Acid in Patients With Hyperlipidemia Not Adequately Controlled by Statins","Inclusion Criteria:\n\n1\\. 18 years and older. 2. 18.5 kg\u002Fm2 ≤Body Mass Index (BMI) ≤35 kg\u002Fm2. 3. Diagnosis with ASCVD or have high-risk ASCVD, and\u002For diagnosis with HeFH.4.Be on stable lipid-modifying therapy for at least 4 weeks prior to screening, including moderate to high-dose statins with or without other lipid-modifying therapy (cholesterol absorption inhibitors\\[ezetimibe, Hyzetimibe\\]，fibrates \\[except gemfibrozil\\]）; 5.Fasting LDL-C must meet any one of the following\n\n1. For participants with high risk of ASCVD: LDL-C ≥ 2.6 mmol\u002FL (or 100 mg\u002FdL);\n2. For participants with extremely high risk of ASCVD: LDL-C≥ 1.8 mmol\u002FL (or 70 mg\u002FdL); 3) For participants with ultra-high risk of ASCVD: LDL-C≥ 1.4 mmol\u002FL (or 55 mg\u002FdL).\n\n6.Fully understand the purpose and requirements of the study, voluntarily participate in the clinical trial, and sign a written informed consent form.\n\nExclusion Criteria:\n\n1. Known allergy to any component of the investigational drug or its excipients or related preparations, or a history of allergic diseases (e.g., asthma, urticaria, eczema) or allergic constitution.\n2. Diagnosis with HoFH.\n3. History of tendon diseases or tendon ruptures before the screening.\n4. Severe, uncontrolled concomitant conditions that may affect drug absorption or have a significant impact on lipid level.\n5. Hyperthyroidism or uncontrolled hypothyroidism\n6. Uncontrolled hypertension\n7. Severe cardiovascular or cerebrovascular events in the past 3 months\n8. History of nephrotic syndrome or glomerulonephritis or severe renal dysfunction.\n9. Liver disease or dysfunction","ALL","18 Years",{"count":19,"type":20},222,"ESTIMATED","INTERVENTIONAL",[23],"PHASE3","This trial is a multicenter randomized, double-blind, placebo-controlled phase III study to evaluate the efficacy and safety of Bempedoic Acid Tablets in patients with hyperlipidemia not adequately controlled by Statins.",[26],"Primary Hyperlipidemia","NOT_YET_RECRUITING","2026-05-29",{"date":30,"type":31},"2026-06-03","ACTUAL",{"date":33,"type":20},"2026-06-12",{"date":35,"type":20},"2027-08-28",{"name":37,"class":38},"CSPC Ouyi Pharmaceutical Co., Ltd.","INDUSTRY",{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":46,"enrollmentInfo":47,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":51,"conditions":52,"keywords":53,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":66},"100579334","phase-2-zhibitai-capsules-for-the-treatment-of-primary-hyperlipidemia-100579334","NCT06822946","Zhibitai Capsules for the Treatment of Primary Hyperlipidemia","Zhibitai Capsules for the Treatment of Primary Hyperlipidemia (Tan yu hu Jie, qi Xue bu li Zheng) A Randomized, Double-blind, Parallel Controlled, Multicenter, Phase II Clinical Trial","Inclusion Criteria:\n\n1. Age between 18 and 75 years old (inclusive), regardless of gender;\n2. BMI (Body Mass Index) between 18.0 kg\u002Fm² and 30.0 kg\u002Fm²;\n3. Meets the diagnostic criteria for primary hyperlipidemia (tan yu hu jie, qi xue bu li zheng);\n4. LDL-C level ≥ 3.4 mmol\u002FL and TG level ≤ 4.5 mmol\u002FL;\n5. Diagnosis before and after the run-in period meets the above criteria, and the absolute difference between the two LDL-C measurements before and after the run-in period does not exceed 12%;\n6. Agrees to follow dietary and lifestyle modification guidance during the trial, maintain a stable diet and exercise routine throughout the study, take medication as required, and complete diary cards;\n7. Agrees to participate in this clinical trial and voluntarily signs the informed consent form.\n\nExclusion Criteria:\n\n1. Known or suspected allergy to any component of the investigational product, or having an allergic constitution.\n2. According to the \"Chinese Guidelines for Lipid Management (2023)\", individuals classified as being at very high risk or extremely high risk for ASCVD.\n3. Confirmed homozygous familial hypercholesterolemia.\n4. Dyslipidemia caused by secondary reasons, such as nephrotic syndrome, hypothyroidism, renal failure, systemic lupus erythematosus, glycogen storage disease, myeloma, lipodystrophy, acute porphyria, polycystic ovary syndrome, drug-induced causes (e.g., phenothiazines, beta-blockers, glucocorticoids, certain contraceptives, etc.), or patients currently using heparin, thyroid hormone therapy, or other medications that affect lipid metabolism.\n5. Any surgical or medical condition that may significantly affect the absorption, distribution, metabolism, or excretion of the drug:\n\n   * History of major gastrointestinal surgery, such as gastrectomy, gastrointestinal anastomosis, or intestinal resection; ② Active or recurrent irritable bowel syndrome (IBS) or inflammatory bowel disease (except for those asymptomatic for at least 6 months prior to the screening visit);\n\n     * Current active gastritis, active ulcer, or gastrointestinal bleeding;\n\n       * History of pancreatic or gallbladder disease (except for those with prior cholecystectomy).\n6. Previous use of proprotein convertase subtilisin\u002Fkexin type 9 (PCSK9) inhibitors, such as evolocumab and alirocumab.\n7. Use of lipid-lowering drugs within 4 weeks prior to enrollment or within 5 half-lives of the drug (whichever is longer), such as statins, cholesterol absorption inhibitors, probucol, bile acid sequestrants, fibrates, niacin, high-purity fish oil preparations, weight-loss drugs (e.g., GLP-1 receptor agonists), and other traditional Chinese medicines, health products, or hospital preparations (e.g., formula granules, herbal decoctions) with clear lipid-lowering effects as stated in the instructions.\n8. History of acute or chronic liver disease, drug-induced liver injury, or cirrhosis (except for mild fatty liver indicated by abdominal ultrasound).\n9. ALT or AST ≥ 2 times the upper limit of normal (ULN), SCr \\> ULN, total bilirubin (TBIL) ≥ 1.5 times ULN, creatine kinase ≥ 3 times ULN, or any other laboratory test result (blood routine, urine routine, blood biochemistry) exceeding the ULN, and judged by the investigator as potentially affecting efficacy or safety evaluation.\n10. History of any of the following severe cardiovascular or cerebrovascular diseases:\n\n    ① Unstable angina or coronary artery bypass grafting within 3 months prior to the screening visit, or percutaneous coronary intervention.\n    * Myocardial infarction, shock, life-threatening arrhythmia, or significant ECG abnormalities (e.g., ST-segment abnormalities, pathological Q waves, abnormal QTc interval, etc.) within 6 months prior to the screening visit.\n\n      * History of left ventricular outflow tract obstruction (e.g., aortic stenosis, idiopathic hypertrophic subaortic stenosis).\n\n        * Heart failure ≥ Class II (NYHA classification) at screening. ⑤ Acute stroke within 6 months prior to the screening visit, excluding asymptomatic stroke.\n11. Uncontrolled hypertension (history of hypertension with regular medication, and two consecutive blood pressure measurements ≥ 180\u002F110 mmHg at screening), or history of type 1 diabetes, diabetic ketoacidosis, or uncontrolled type 2 diabetes (HbA1c \\> 7%).\n12. Patients with other severe metabolic diseases.\n13. History of myositis, myopathy, or rhabdomyolysis, severe muscle abnormalities, and neuropathy.\n14. Thyroid dysfunction (e.g., hyperthyroidism, hypothyroidism, etc.) (except for those judged by the investigator as clinically insignificant).\n15. Proven intolerance or inefficacy to HMG-CoA reductase inhibitors.\n16. History of malignancy within 5 years prior to the first dose, excluding cervical epithelial carcinoma, squamous cell carcinoma, or basal cell carcinoma of the skin that has been clinically cured for 5 years.\n17. Pregnant or lactating women, or individuals of either gender with plans for pregnancy within the next 3 months.\n18. Suspected or confirmed history of alcohol, drug, or substance abuse.\n19. Individuals with special dietary requirements who cannot adhere to the required diet and exercise control, including but not limited to those following extreme weight-loss diets, undergoing or planning to undergo intense exercise programs (e.g., marathon training, fitness training), or intending to start such training during the trial.\n20. Positive for any of the following: hepatitis B virus surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody, or syphilis-specific antibody (TPHA).\n21. Participation in other interventional clinical trials within the past 3 months.\n22. Individuals deemed unsuitable for participation in this clinical trial by the investigator.","75 Years",{"count":48,"type":20},192,[50],"PHASE2","Exploring the benefit risk ratio of increase in dosage of Zhibitai capsules (2 capsules at a time, 2 times a day) compared to the original dosage (1 capsule at a time, 1 day)",[26],[54,55],"zhibitai","primary hyperlipidemia","RECRUITING","2025-11-18",{"date":59,"type":31},"2025-11-20",{"date":61,"type":31},"2025-03-27",{"date":63,"type":20},"2026-04-30",{"name":65,"class":38},"Chengdu Diao Jiuhong Pharmaceutical Factory",1,{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":74,"targetDuration":4,"studyType":21,"phases":76,"briefSummary":77,"conditions":78,"keywords":79,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":66},"100576063","phase-3-a-clinical-study-to-evaluate-the-efficacy-tolerability-and-safety-of-bempedoic-acid-100576063","NCT06780410","A Clinical Study to Evaluate the Efficacy, Tolerability, and Safety of Bempedoic Acid","A Phase III Clinical Study to Evaluate the Efficacy, Tolerability, and Safety of Bempedoic Acid in Patients with Hyperlipidemia Not Adequately Controlled by Statins","Inclusion Criteria:\n\n* 1\\. 18 years and older, male or female.\n* 2\\. 18 kg\u002Fm2 ≤Body Mass Index (BMI) ≤35 kg\u002Fm2.\n* 3\\. Participants must agree to use reliable contraception from the screening day until 30 days after the last dose, and must not donate sperm or eggs for assisted reproduction purposes.\n* 4\\. Fully understand the purpose and requirements of the study, voluntarily participate in the clinical trial, and sign a written informed consent form, capable of completing the entire study process.\n\nExclusion Criteria:\n\n* 1\\. Known allergy to any component of the investigational drug or its excipients, or a history of allergic diseases (e.g., asthma, urticaria, eczema) or allergic constitution.\n* 2\\. Fasting triglycerides (TG) ≥ 5.64 mmol\u002FL (≥ 500 mg\u002FdL) at screening.\n* 3\\. History of malignant tumors prior to screening.\n* 4\\. History of drug, alcohol, amphetamines, or other drug abuse.\n* 5\\. Participation in other clinical studies and use of other investigational drugs or medical devices within 3 months prior to screening or within 5 half-lives of the drugs (whichever is longer).\n* 6\\. Pregnant or breastfeeding females, or those with a positive human chorionic gonadotropin (HCG) pregnancy test.\n* 7\\. Any other factors that the investigator believes makes the participant unsuitable for the study.",{"count":75,"type":20},240,[23],"This trial is a phase III study to evaluate the efficacy , tolerability, and safety of Bempedoic Acid Tablets in patients with hyperlipidemia not adequately controlled by Statins.",[26],[80,81,82,83],"Bempedoic Acid","Hyperlipidemia","Efficacy","Safety","2025-01-13",{"date":86,"type":31},"2025-01-17",{"date":88,"type":31},"2024-12-20",{"date":90,"type":20},"2025-10",{"name":92,"class":38},"Gan & Lee Pharmaceuticals."]