[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Alebund Pharmaceuticals\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":71},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100587829","phase-3-a-study-of-a-novel-iron-based-phosphate-binder-ap301-in-patients-with-hyperphosphatemia-in-the-us-and-china-100587829",false,"NCT06933472","A Study of a Novel Iron-based Phosphate Binder AP301 in Patients With Hyperphosphatemia in the U.S. and China","A Randomized, Double-Blind, Multi-Regional, Phase 3 Study to Evaluate the Efficacy and Safety of AP301 on Serum Phosphorus Control in Chronic Kidney Disease Patients Receiving Maintenance Dialysis With Hyperphosphatemia","RESPOND-2","Key Inclusion Criteria:\n\n* Provision of signed and dated ICF\n* Age ≥ 12 years when signing the ICF\n* Patients on dialysis for ≥ 3 months before signing the ICF and throughout the study\n* For HD patients, spKt\u002FV ≥ 1.2; for PD patients, total Kt\u002FV ≥ 1.7\u002Fweek\n* Patients who receive phosphate-lowering drugs over 4 weeks and their serum phosphate level is:\n\n  1. Screening: 1.13 mmol\u002FL (3.5 mg\u002FdL) ≤ serum phosphate \\\u003C 2.58 mmol\u002FL (8.0 mg\u002FdL)\n  2. After washout: 1.94 mmol\u002FL (6.0 mg\u002FdL) ≤ serum phosphate \\\u003C 3.23 mmol\u002FL (10.0 mg\u002FdL)\n\nKey Exclusion Criteria:\n\n* History or plan of kidney transplantation\n* History or plan of parathyroid intervention 6 months before signing the ICF\n* Serum calcium \\\u003C 1.9 mmol\u002FL (7.6 mg\u002FdL) or \\> 2.75 mmol\u002FL (11 mg\u002FdL) at screening\n* Serum intact parathyroid hormone \\> 127 pmol\u002FL (1200 pg\u002FmL) at screening\n* Presence of clinically significant gastrointestinal (GI) disorder\n* History of gastrectomy or duodenectomy, or GI surgery within 3 months before signing the ICF\n* Known allergic to any ingredient of AP301, or known history of severe allergies leading to emergency medical care\n* Female who are breastfeeding","ALL","12 Years",{"count":20,"type":21},264,"ESTIMATED","INTERVENTIONAL",[24],"PHASE3","The goal of this clinical trial is to learn if AP301 could work in the patients receiving maintenance dialysis with elevated blood phosphate. The main questions it aims to answer are:\n\n* Does AP301 lower blood phosphate levels?\n* Does AP301 works on serum calcium level, calcium times phosphate level, and intact parathyroid hormone level?\n* What discomfort or medical problem do the patients have when taking AP301?\n* Does AP301 improve quality of life in Chinese patients?\n\nThe researchers will compare AP301 to an ineffective comparator (a look-alike substance that contains low dose AP301) to see if AP301 works to treat elevated blood phosphate.\n\nIn the study, the patients will experience the following stages in a chronicle order:\n\n* Stop all using blood phosphate-lowering drugs,\n* Take AP301 or the comparator three times a day for 8 weeks,\n* Take AP301 three times a day for 24 weeks, and\n* Take AP301 or the comparator three times a day for 3 weeks.\n\nIn the first 32 weeks, the dose of AP301 will be adjusted upwards or downwards based on the patient's blood phosphate level and the study doctor's judgment.\n\nIf the participant has a blood phosphate level above or below a certain level, they may receive additional treatment to lower the blood phosphate level.",[27,28,29,30],"Hyperphosphatemia","Chronic Kidney Disease, Receiving Dialysis","ESRD (End-Stage Renal Disease)","Dialysis",[27,32,30,33],"AP301","ESKD","RECRUITING","2026-01-28",{"date":37,"type":38},"2026-01-29","ACTUAL",{"date":40,"type":38},"2025-06-13",{"date":42,"type":21},"2027-01-10",{"name":44,"class":45},"Alebund Pharmaceuticals","INDUSTRY",42,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":70},"100567291","phase-1-a-study-to-evaluate-the-safety-tolerability-pk-and-pd-of-ap303-in-dkd-patients-100567291","NCT06666283","A Study to Evaluate the Safety, Tolerability, PK and PD of AP303 in DKD Patients","A Randomized, Double-blind, Placebo-controlled Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AP303 Following 2-week Oral Administration in Diabetic Kidney Disease Patients With Renal Impairment.","Inclusion Criteria:\n\n1. Male and female participants, ≥30 years of age at the time of signing the informed consent form.\n2. BMI (body mass index) 18-30 kg\u002Fm².\n3. Patient has a clinical diagnosis of Type 2 Diabetes Mellitus and is taking at least one type of hypoglycemic drugs, before screening visits, the doses of hypoglycemic drugs, including insulin, need to be stable for at least two weeks..\n4. Patient must be on a stable dose of angiotensin converting anzyme inhibitior (ACEI) or Angiotensin II receptor blockers (ARB) for at least 4 weeks prior to screening.\n5. Hemoglobin A1c ≥6.5% but ≤10.5% at the screening visit.\n6. Estimated GFR ≥30 mL\u002Fmin\u002F1.73m² but \\\u003C 60 mL\u002Fmin\u002F1.73m² at the screening visit.\n7. Urinary albumin to creatinine ratio ≥ 30 mg\u002Fg at the screening visit.\n\nExclusion Criteria:\n\n1. Chronic kidney disease other than type 2 diabetic kidney disease.\n2. Patient receiving corticosteroid immunotherapy or other immunosuppressants (such as calcineurin inhibitors ciclosporin, cyclophosphamide, or mycophenolate mofetil) in the past 3 months before screening.\n3. Recently having acute kidney injury or received renal surgery within the last 6 months before screening visit, or have received renal transplantation.\n4. Congestive heart failure classified New York Heart Association (NYHA) class II to IV within the last 3 months before the screening visit.\n5. Peripheral edema above the ankle level at the screening or randomization visit.\n6. Confirmed (based on the average of 2 separate resting blood pressure measurements in a sitting position, after at least 5 minutes rest) systolic BP greater than 160 or less than 90 mmHg, and diastolic BP greater than 100 or less than 50 mmHg at screening.\n7. Myocardial infarction, acute coronary syndrome, stroke or transient ischemic attack, cardiovascular surgery within 6 months prior to the screening visit.\n8. Abnormalities of ECG parameters and abnormal shape of ECG wave on screening ECG: e.g.\n\n   * QTc interval (QTcF \\> 450 ms for male and QTcF \\> 470 ms for female) based on the average interval on triplicate ECGs obtained after 5 minute's rest in a supine position\n   * Notable resting bradycardia (mean HR \\\u003C 40 bpm)\n   * Notable resting tachycardia (mean HR \\> 100 bpm)\n   * ECG with QRS and\u002For T wave judged to be unfavorable for a consistently accurate QT measurement (e.g., neuromuscular artifact that cannot be readily eliminated, indistinct QRS onset, low amplitude T wave, merged T- and U-waves, prominent U waves)\n   * Any other significant abnormality\n9. Implantation of cardiac pacemaker or clinically significant arrhythmia, e.g. atrial fibrillation, atrial flutter, right or left bundle branch block, Wolf-Parkinson-White Syndrome.\n10. Current or previous treatment with a thiazolidinedione (e.g., medications containing pioglitazone or rosiglitazone, like Actos, Avandia, ActoplusMet, Avandamet, Avandaryl), PPARa agonist (like fenofibrate) or any dual\u002Fmultiple PPARa\u002Fg agonist (e.g., Chiglitazar Sodium) in the 3 months preceding screening visit.\n11. Previous treatment with CYP2C8 inducer or strong\u002Fmoderate inhibitor (refer to the list in Appendix 4) in the 1 month preceding screening visit.\n12. Chronic therapy with non-steroidal anti-inflammatory drugs (NSAIDs) (except prophylactic stable low dose aspirin, defined as its dose not higher than 100 mg daily; paracetamol\u002Facetaminophen was allowed) in the last month before screening.\n13. ALT or AST \\>1.5 × ULN, or laboratory tests revealed other clinically significant abnormalities in liver function at screening.\n14. Creatine phosphokinase (CPK) elevated \\> 3 x ULN at screening visit or history of drug-induced myopathy.\n15. History of malignancy within 5 years before screening (exceptions: squamous and basal cell carcinomas of the skin and carcinoma of the cervix in situ, or a malignancy that in the opinion of the investigator, with concurrence with the sponsor's medical monitor, is considered cured with minimal risk of recurrence).\n16. Participants who have had significant acute infection, e.g., COVID-19, influenza, local infection, acute gastrointestinal symptoms or any other clinically significant illness within two weeks before study drug administration.\n17. Positive test at screening of any of the following: Hepatitis B (HBsAg), Hepatitis C (HCVAb), human immunodeficiency virus (HIV Ab) or syphilis AB.\n18. Dosed with a small-molecule investigational drug within 3 months, or biologic investigational drug within 3 months or 5 half-lives (whichever is the longer) prior to first dose of this study.\n19. History of drug and\u002For alcohol abuse or addiction. History (within 3 months of screening) of alcohol consumption exceeding 3 and 2 standard drinks per day on average (1 standard drink = 10 grams of alcohol) for male and female, respectively.\n20. Within 2 weeks prior to admission, use of \\>5 cigarettes or equivalent nicotine-containing product per day.\n21. Medical or social conditions that would potentially interfere with the participant's ability to comply with the study visit schedule or the study assessments.","30 Years",{"count":56,"type":21},18,[58],"PHASE1","The study will be a single center, double-blind, randomized, placebo-controlled study to evaluate the safety, tolerability, PK and PD of AP303 following 2-week oral administration to Diabetic Kidney Disease patients.",[61],"Diabetic Kidney Disease","2025-09-05",{"date":64,"type":38},"2025-09-11",{"date":66,"type":38},"2025-02-27",{"date":68,"type":21},"2025-09-25",{"name":44,"class":45},1,""]