[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jiangsu Aosaikang Pharmaceutical Co., Ltd.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":117},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,68,91],{"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":39},"100601364","phase-3-askc202-combined-with-limertinib-versus-platinum-based-chemotherapy-in-treatment-of-locally-advanced-or-metastatic-nsclc-with-met-amplificationoverexpression-after-failure-of-egfr-tki-therapy-100601364",false,"NCT07109531","ASKC202 Combined With Limertinib Versus Platinum-based Chemotherapy in Treatment of Locally Advanced or Metastatic NSCLC With MET Amplification\u002FOverexpression After Failure of EGFR-TKI Therapy","A Randomized, Controlled, Open-Label, Multicenter, Phase 3 Study to Evaluate the Efficacy and Safety of ASKC202 in Combination With Limertinib Versus Platinum-based Chemotherapy in Participants With MET Amplification\u002FOverexpression Locally Advanced or Metastatic NSCLC Who Have Failed After Prior EGFR-TKI Therapy.","Inclusion Criteria:\n\n1. Willing and able to provide signed and dated informed consent;\n2. Patients at least 18 years of age;\n3. Locally advanced or metastatic non-small cell lung cancer (NSCLC);\n4. Objective disease progression following prior EGFR-TKI therapy;\n5. EGFR mutation with MET amplification\u002FOverexpression by a central laboratory;\n6. Measurable lesions based on RECIST 1. 1;\n7. ECOG performance status 0 or 1;\n8. Expected survival \\>12 weeks;\n9. Adequate bone marrow reserve or organ function.\n\nExclusion Criteria:\n\n1. Prior or ongoing treatment with any c-Met target;\n2. Previously received systemic chemotherapy;\n3. Patients requiring continuous use of systemic immunosuppressants or systemic corticosteroids within 2 weeks prior to the first dose.\n4. Patients who underwent other major surgical procedures other than diagnosis or biopsy within 4 weeks prior to the first dose, or who were expected to undergo major surgeries during the study period;\n5. Prior to the first administration, there are unhealed toxic reactions of ≥ grade 2 (CTCAE 5.0 standard) associated with any previous treatment, any level of hair loss, and platinum drugs Except for grade 2 neuropathy caused;\n6. Patients with leptomeningeal metastasis, brainstem metastasis, or spinal cord compression;\n7. Presence of dysphagia or gastrointestinal disorders that may interfere with oral medication absorption;\n8. Previous history includes interstitial lung disease (ILD), drug-induced ILD, radiation pneumonitis requiring steroid therapy, or evidence of clinically active ILD；\n9. Have previously received hematopoietic stem cell transplants or solid organ transplants, or plan to receive hematopoietic stem cell transplants or solid organ transplants during the current period of study;\n10. There are serious or active infections that required intravenous antibiotics or hospitalization, such as HBV (HBsAg-positive and peripheral HBV-DNA titer test≥1×104 copies\u002FmL or 2000 IU\u002FmL), HCV, HIV, and syphilis;\n11. Serious or uncontrolled cardiovascular disease;\n12. Pregnant or lactating females;\n13. Other primary malignancies have been diagnosed within the last 5 years, and the following conditions can be enrolled: non-melanoma skin cancer, superficial bladder cancer, cervical carcinoma in situ that has undergone surgery and has been cured;","ALL","18 Years",{"count":19,"type":20},286,"ESTIMATED","INTERVENTIONAL",[23],"PHASE3","This study is designed to compare the safety and efficacy of ASKC202 combined with Limertinib Versus platinum-based chemotherapy in locally advanced or metastatic NSCLC With MET Amplification\u002FOverexpression after disease progression on EGFR tyrosine kinase inhibitor.",[26],"Locally Advanced or Metastatic NSCLC","RECRUITING","2026-08-17",{"date":30,"type":31},"2026-08-19","ACTUAL",{"date":33,"type":31},"2025-08-04",{"date":35,"type":20},"2028-12-31",{"name":37,"class":38},"Jiangsu Aosaikang Pharmaceutical Co., Ltd.","INDUSTRY",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":47,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":51,"conditions":52,"keywords":55,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":39},"100651395","phase-2-ask0912-versus-polymyxin-b-for-injection-in-adults-with-hospital-acquired-or-ventilator-associated-bacterial-pneumonia-100651395","NCT07759934","ASK0912 Versus Polymyxin B for Injection in Adults With Hospital-Acquired or Ventilator-Associated Bacterial Pneumonia","A Multicenter, Randomized, Open-label Phase 2 Study to Evaluate the Efficacy and Safety of ASK0912 for Injection Versus Polymyxin B for Injection in Adult Patients With Hospital-acquired Bacterial Pneumonia\u002FVentilator-associated Bacterial Pneumonia","Inclusion Criteria:\n\n* 1\\. Aged 18-75 years on the day of informed consent signature;\n* 2\\. Require intravenous antibiotic therapy for hospital-acquired bacterial pneumonia (HABP)\u002Fventilator-associated bacterial pneumonia (VABP).\n* 3\\. At least one clinical sign or symptom of HABP\u002FVABP.\n* 4\\. At least one laboratory abnormality of HABP\u002FVABP.\n* 5\\. Chest imaging at screening demonstrating new or progressive infiltrates consistent with pneumonia.\n* 6\\. APACHE II score ≤ 30.\n* 7\\. Appropriate lower respiratory tract specimen obtained at screening for Gram stain and bacterial culture.\n* 8\\. Subjects receiving HABP\u002FVABP-active antibiotics within 72h pre-enrollment may enroll if ≤24h therapy, or ≥48h with persistent\u002Fworsening HABP\u002FVABP signs\u002Fsymptoms at screening.\n* 9\\. Women of childbearing potential must have a negative pregnancy test (serum or urine) prior to enrollment.\n* 10\\. Male subjects must use highly effective contraception throughout the study period.\n\nExclusion Criteria:\n\n* 1\\. Subjects with known allergy to polymyxins or carbapenems, regardless of the severity of the reaction; or subjects with a severe hypersensitivity reaction to any other β-lactam agent.\n* 2\\. Subjects who have received any investigational product within 3 months prior to enrollment, or subjects who have previously participated in this clinical study.\n* 3\\. Has a baseline lower respiratory tract specimen Gram stain that shows the presence of Gram-positive cocci only.\n* 4\\. Known or suspected pneumonia caused by Mycoplasma, Chlamydia, Legionella, fungi, parasites, viruses, or chemical etiologies (including gastric aspiration, inhalation injury).Additionally, subjects with confirmed or suspected community-acquired bacterial pneumonia (CABP) are excluded.\n* 5\\. Presence of underlying pulmonary conditions that may interfere with efficacy assessment, such as pulmonary tuberculosis, lung abscess, empyema, obstructive pneumonia, granulomatous disease, recent pulmonary embolism, moderate-to-severe bronchiectasis, severe chronic obstructive pulmonary disease, bronchial obstruction, idiopathic interstitial pneumonia, etc.\n* 6\\. Presence of other active infections that may interfere with efficacy assessment, or bacterial infectious foci requiring concomitant treatment with antibacterial agents prohibited by the study protocol, such as invasive fungal infection, endocarditis, central nervous system infection (e.g., meningitis, brain abscess, post-shunt infection), septic arthritis requiring vancomycin, etc.\n* 7\\. Severe cardiac disorders, including severe arrhythmia, significant myocardial ischemia, congestive heart failure classified as NYHA Class III-IV.\n* 8\\. Subjects with liver cirrhosis classified as Child-Pugh Class C.\n* 9\\. Subjects with documented immunodeficiency or impaired immune function, including HIV infection, hematological malignancies, bone marrow transplantation, etc.; or subjects receiving immunosuppressive therapy, including immunosuppressants, chemotherapeutic agents, drugs for prevention of transplant rejection, and corticosteroids (prednisone ≥ 20 mg\u002Fday for more than 14 days).\n* 10\\. Presence of any one of the following abnormalities: aspartate aminotransferase (AST) and\u002For alanine aminotransferase (ALT) \\> 5 × upper limit of normal (ULN); AST and\u002For ALT \\> 3 × ULN accompanied by total bilirubin \\> 1.5 × ULN; creatinine clearance \\\u003C 80 mL\u002Fmin (calculated using the Cockcroft-Gault formula); absolute neutrophil count \\\u003C 1 × 10⁹\u002FL; platelet count \\\u003C 60 × 10⁹\u002FL.\n* 11\\. Subjects with a history or evidence of severe renal disease, or receiving hemodialysis or peritoneal dialysis.\n* 12\\. Subjects presenting with shock.\n* 13\\. Subjects scheduled to undergo major surgery during the study period.\n* 14\\. Subjects with a known history of epilepsy or neuromuscular junction disorders such as myasthenia gravis.\n* 15\\. Subjects with any past or current disease, treatment, laboratory abnormality, or other condition that, in the investigator's opinion, may compromise the quality of study data or increase treatment risks during the study, e.g., subjects requiring valproic acid therapy during the study.\n* 16\\. Subjects with any psychiatric or psychological disorder judged by the investigator to potentially increase trial risks, impair protocol compliance, or hinder study completion, such as recent (within the past 12 months) or active suicidal ideation\u002Fbehavior.\n* 17\\. Subjects judged by the investigator on clinical assessment to be at risk of death within the 7-14-day treatment phase despite adequate antibiotic therapy for pneumonia.\n* 18\\. Female subjects who are breastfeeding or plan to breastfeed prior to the end of the study.\n* 19\\. Any other conditions rendering the subject unsuitable for participation in this study as determined by the investigator.",{"count":48,"type":20},60,[50],"PHASE2","This is a randomized, active-controlled, multicenter phase II clinical trial. The study aims to evaluate the efficacy, safety and tolerability of two different dosing regimens of ASK0912 for Injection compared with Polymyxin B Sulfate for Injection in adult patients with hospital-acquired bacterial pneumonia (HABP) or ventilator-associated bacterial pneumonia (VABP) caused by multidrug-resistant or carbapenem-resistant Gram-negative bacilli. Eligible subjects will be randomly assigned to one of three treatment groups: ASK0912 Regimen 1, ASK0912 Regimen 2, or Polymyxin B Sulfate active comparator group. Subjects will receive assigned intravenous study treatment for 7 to 14 days. The primary efficacy endpoints include clinical cure rate at the Test of Cure (TOC) visit and Day 28 all-cause mortality in the modified intent-to-treat (MITT) population. Safety assessments will be conducted throughout the study to monitor adverse events, laboratory parameters and other safety indicators.",[53,54],"Ventilator-associated Bacterial Pneumonia (VABP)","Hospital-acquired Bacterial Pneumonia (HABP)",[56,57,58,59],"Hospital-Acquired Bacterial Pneumonia","Ventilator-Associated Bacterial Pneumonia","Polymyxin B","ASK0912","2026-08-09",{"date":62,"type":31},"2026-08-12",{"date":64,"type":31},"2026-03-25",{"date":66,"type":20},"2027-12-25",{"name":37,"class":38},{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":21,"phases":77,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},"100462780","phase-1-study-to-assess-the-safety-tolerability-pharmacokinetics-and-preliminary-anti-tumor-activity-of-askc202-with-or-without-ask120067-100462780","NCT05306132","Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumor Activity of ASKC202 With or Without ASK120067","A Phase I ,Open, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumor Activity of ASKC202 With or Without ASK120067 in Patients With Advanced Solid Tumors","Inclusion Criteria:\n\n1. Willing and able to provide signed and dated informed consent;\n2. Aged 18 years old or more, male or female;\n3. Part 1 (Monotherapy Dose-Escalation) and Part 3 (Monotherapy Expansion): the subjects with locally advanced or metastatic solid tumors for whom no standard therapy regimens are available currently or who are intolerable to standard therapy regimens; Part 3: the subjects with MET gene amplification or protein overexpression; Part 3 cohort 1: histologically or cytologically confirmed unresectable locally advanced or metastatic NSCLC.\n\n4）Part 2:(Combination Therapy Dose-Escalation):a)histologically or cytologically confirmed unresectable locally advanced or metastatic NSCLC;b)Histologically confirmed EGFR sensitizing mutation (Ex19del or L858R).；c)Disease progression following treatment with a third-generation EGFR TKI, or treatment with a first-\u002Fsecond-generation EGFR-TKI with confirmed T790M-negative status upon progression; d)MET gene amplification or protein overexpression.\n\n5\\) Part 4:(Combination Therapy Dose-Expansion):a)histologically or cytologically confirmed unresectable locally advanced or metastatic NSCLC;b)Histologically confirmed EGFR sensitizing mutation (Ex19del or L858R).；c)MET gene amplification or protein overexpression.\n\n6\\) At least one measurable lesion (based on the RECIST 1.1 criterion) (this article is only for the dose expansion phase); 7) ECOG score 0\\~1; 8) Expected survival time ≥ 3 months; 9) Major organ function is essentially normal (no transfusions, erythropoietin (EPO), granulocyte colony-stimulating factor (G-CSF), or other medically supportive care have been received in the 14 days prior to the administration of the study drug), and laboratory tests during the screening period meet the following criteria: system Laboratory test values haematology Absolute neutrophil count ≥1.5 ×109\u002FL platelet ≥90×109\u002FL haemoglobin ≥90g\u002FL kidney Serum creatinine or Creatinine clearance (CrCl). ≤ 1.5 × ULN or\n\n≥60 mL\u002Fmin (estimated from the Cockcroft-Gault formula) liver Total bilirubin ≤1.5 × ULN or ≤2 × ULN (for patients with liver cancer or liver metastases). AST(SGOT) and ALT (SGPT). ≤2.5 × ULN or ≤5 × ULN (for patients with liver cancer or liver metastases). Coagulation (no anticoagulation was received in the 7 days prior to the administration of the study drug).\n\nInternational normalized ratio (INR) or prothrombin time (PT). ≤1.5 × ULN Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN 10) Women of childbearing age must have a pregnancy test (serum or urine) within 7 days of enrolling and have a negative result, or meet one of the following criteria to prove that there is no risk of pregnancy: a Postmenopausal is defined as amenorrhea at least 12 months after age \\>50 years and discontinuation of all exogenous hormone replacement therapy; b Women younger than 50 years of age who are considered postmenopausal if they have been amenorrhea for 12 months or more after stopping all exogenous hormone therapy, and luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels are within the laboratory reference values for postmenopausal; c Previously undergone irreversible sterilization procedures, including hysterectomy, bilateral ovarian resection, or bilateral salping, with the exception of bilateral tubal ligation; 11) Women of childbearing age should use strict contraceptive contraception throughout trial 7 and within 3 months after the last dose of the test drug; male subjects should use strict contraception throughout the trial period and for 6 months after the last dose of the test drug and no sperm donation; 12) The patient understands the purpose and steps of the trial, voluntarily participates in the trial, and signs a written informed consent form; 13) Patients have good comprehension, are able to follow protocol requirements and can cooperate with investigators in this trial.\n\nExclusion Criteria:\n\n1. Have previously received or are receiving any treatment for c-Mets (including all monoclonal antibodies or small molecule drugs targeted at the target, except for crizotinib);\n2. Have received chemotherapy, hormone therapy, immunotherapy, or biological therapy such as antibody therapy within 4 weeks prior to the first dose, or traditional Chinese medicine with anti-tumor indications within 2 weeks, or small molecule targeted therapy with an interval of less than 5 half-lives; palliative radiotherapy within 7 days or extensive\u002Ftherapeutic radiotherapy within 14 days prior to the first dose;\n3. Those who still need to continue to use systemic immunosuppressants or systemic corticosteroids (≥ 10 mg of prednisone or its equivalent other corticosteroid) for 2 weeks prior to the first dose;\n4. Patients who have used strong inhibitors or strong inducers of CYP3A within 2 weeks prior to the first administration, or who need to continue treatment with these drugs during the study period;\n5. Participation in clinical trials of other drugs within 4 weeks prior to the first administration (except for failed screening);\n6. Patients who underwent other major surgical procedures other than diagnosis or biopsy within 4 weeks prior to the first dose, or who were expected to undergo major surgeries during the study period;\n7. Prior to the first administration, there are unhealed toxic reactions of ≥ grade 2 (CTCAE 5.0 standard) associated with any previous treatment, any level of hair loss, and platinum drugs Except for grade 2 neuropathy caused;\n8. Patients with primary central nervous system tumors or central nervous system metastases including meningeal metastases (except those who are asymptomatic and stable, do not require steroid use for at least 4 weeks before the first dose);\n9. Gastrointestinal disorders (e.g., Crohn's disease, ulcerative colitis, intestinal obstruction, short bowel syndrome) or other malabsorption conditions that have difficulty swallowing or affect drug absorption;\n10. There are any other serious or uncontrolled acute and chronic diseases, such as severe or uncontrollable liver or kidney disease (except liver and kidney cancer), uncontrollable hypertension (blood pressure \\> 150\u002F95 mmHg after antihypertensive therapy), and Acute pancreatitis, uncontrollable hyperglycemia (fasting blood glucose \\>8.0 mmol\u002FL after hypoglycemic therapy), severe or uncontrolled eye lesions, etc\n11. Previous history includes interstitial lung disease (ILD), drug-induced ILD, radiation pneumonitis requiring steroid therapy, or evidence of clinically active ILD\n12. Have previously received hematopoietic stem cell transplants or solid organ transplants, or plan to receive hematopoietic stem cell transplants or solid organ transplants during the current period of study;\n13. If not controlled, large pleural effusions, pericardial effusions, or ascites that need to be drained still need;\n14. There are serious or active infections that required intravenous antibiotics or hospitalization, such as HBV (HBsAg-positive and peripheral HBV-DNA titer test≥1×10\\^4 copies\u002FmL or 2000 IU\u002FmL), HCV, HIV, and syphilis\n15. Meets any of the following cardiac criteria:\n\n    a Average QTc interval prolongation of 3 ECG examinations at rest (QTcF: 450 ms\\> for men \\> 470 ms for women, corrected by Fredericcia's formula); b Presence of uncontrolled or symptomatic arrhythmias, familial arrhythmias, or congenital long QT syndromes; c Had undergone coronary angioplasty, stent implantation, and coronary artery bypass grafting within 6 months before admission; d Myocardial ischemia or myocardial infarction, unstable angina within 6 months before admission; e Judged to be class III-IV congestive heart failure according to the New York Heart Association's cardiac function grade; f Echocardiography (ECHO) shows a left ventricular ejection fraction (LVEF) ≤ 50%;\n16. allergies, or a previous history of severe allergies, or known allergies to any of the components of the drug under study;\n17. Pregnant, Lactating women;\n18. Other primary malignancies have been diagnosed within the last 5 years, and the following conditions can be enrolled: non-melanoma skin cancer, superficial bladder cancer, cervical carcinoma in situ that has undergone surgery and has been cured;\n19. Alcohol abuse, substance abuse, and other conditions that may increase the risk of the study or may interfere with study execution and analysis of results, or that the investigator believes that there are other reasons for which they are not suitable for this clinical study.",{"count":76,"type":20},150,[78],"PHASE1","This study is the first-in-human of ASKC202, which is an open-label, non-randomized, multicenter study with a dose escalation phase and a dose expansion phase.",[81],"Advanced Solid Tumor","2025-12-16",{"date":84,"type":31},"2025-12-23",{"date":86,"type":31},"2022-08-08",{"date":88,"type":20},"2027-12",{"name":37,"class":38},3,{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":97,"eligibilityCriteria":98,"healthyVolunteers":11,"sex":16,"minAge":99,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":39},"100563318","phase-1-the-safety-and-pharmacokinetics-of-askc200-in-osteoarthritic-knee-pain-100563318","NCT06614608","The Safety and Pharmacokinetics of ASKC200 in Osteoarthritic Knee Pain","A Multi-Center, Randomized, Double-blind Phase I Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Efficacy of ASKC200 in Patients with Osteoarthritic Knee Pain","ASKC200","Inclusion Criteria:\n\n1. Sign informed consent prior to any inspection and evaluation, and understand and follow test requirements;\n2. Age 40-75 years old (including boundary value) at the time of signing the informed consent, gender is not limited;\n3. Primary knee osteoarthritis was confirmed by clinical and imaging examination;\n4. Knee osteoarthritis pain history ≥6 months;\n5. Tibial joint X-ray within 3 months prior to drug administration showed that the tibiofemoral joint of the target knee was graded Kellgren-Lawrence II or III;\n6. Before the first medication, the WAADPI NRS score of the study knee was ≥5, and the WAADPI NRS score of the contralateral knee was \\\u003C4;\n7. Be willing to discontinue the use of nonsteroidal anti-inflammatory drugs, acetaminophen, and other pain medications, and only use the acetaminophen provided in the study for emergency treatment of knee osteoarthritis pain during the study period;\n8. Body mass index (BMI) ≤40.0 kg\u002Fm2.\n\nExclusion Criteria:\n\n1. Secondary arthritis caused by other causes;\n2. The study knee has other knee pathologic findings confirmed by clinical evaluation or imaging\n3. There are other conditions that can cause study knee pain or other physical pain;\n4. Other medications for osteoarthritis were used within 1 week prior to the first dose;\n5. Patients with chronic pain in other parts of the body requiring long-term oral analgesic therapy, or those requiring combined treatment with systemic glucocorticoids;\n6. Open knee injury or knee surgery occurred in the study knee within 6 months before the first medication; Or have had any major surgical procedures within 3 months prior to the first medication;\n7. The study knee has received intra-articular injection treatment (such as steroids or sodium hyaluronate, etc.) within 3 months before the first medication;\n8. Received physical therapy for study knee osteoarthritis (such as electrotherapy or acupuncture) within 3 months before the first medication;\n9. Used any capsaicin-containing product or non-steroidal anti-inflammatory drug on the knee within 2 weeks prior to the first administration;\n10. Have An open wound, skin erythema or edema, skin infection, or any other skin lesion in the study knee prior to initial administration;\n11. A history of alcohol or drug dependence within 12 months prior to the first administration or a positive urine drug test during the screening period.","40 Years","75 Years",{"count":102,"type":20},24,[78],"This is a multi-center, randomized, double-blind clinical trial to evaluate the safety, tolerability, pharmacokinetics, and efficacy of ASKC200 in subjects with OA of the knees and determine the phase II recommended dose. Assigned doses will be applied for 60 minutes on each of four consecutive days.",[106,107],"Osteoarthritis, Knee","Pain","NOT_YET_RECRUITING","2024-09-25",{"date":111,"type":31},"2024-09-27",{"date":113,"type":20},"2024-10",{"date":115,"type":20},"2025-12",{"name":37,"class":38},""]