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: * Does AP301 lower blood phosphate levels? * Does AP301 works on serum calcium level, calcium times phosphate level, and intact parathyroid hormone level? * What discomfort or medical problem do the patients have when taking AP301? * Does AP301 improve quality of life in Chinese patients? The 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. In the study, the patients will experience the following stages in a chronicle order: * Stop all using blood phosphate-lowering drugs, * Take AP301 or the comparator three times a day for 8 weeks, * Take AP301 three times a day for 24 weeks, and * Take AP301 or the comparator three times a day for 3 weeks. In 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. If the participant has a blood phosphate level above or below a certain level, they may receive additional treatment to lower the blood phosphate level.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
264
Three times a day, administered orally with three meals at a daily dose level from 2.7g to 9.0g
Three times a day, administered orally with three meals at a daily dose level from 0.075g to 0.25g
Renal Consultants Medical Group
Granada Hills, California, United States
RECRUITINGNorth America Research Institute - San Dimas
San Dimas, California, United States
RECRUITINGNorth America Research Institute - San Dimas
San Dimas, California, United States
RECRUITINGRocky Mountain Kidney Care - Lone Tree
Lone Tree, Colorado, United States
Change in serum phosphate concentrations in the AP301 and the AP301 low dose groups
The amount of phosphate in the blood will be measured with a standard laboratory test. The change in phosphate levels will be compared between the group receiving AP301 and the group receiving AP301 low dose.
Time frame: From Baseline to the end of Week 8
Chang in serum phosphate concentrations in the AP301 maintenance dose and the AP301 low dose groups
The amount of phosphate in the blood will be measured with a standard laboratory test. The change in phosphate levels will be compared between the group receiving AP301 maintenance dose and the group receiving AP301 low dose.
Time frame: From the beginning of Week 33 to the end of Week 35
Change in serum phosphate concentrations over time throughout the study
Time frame: From Baseline to the end of Week 35
Change in serum calcium (Ca) and intact parathyroid hormone levels over time
The amount of calcium and intact parathyroid hormone (iPTH) in the blood will be measured with standard laboratory tests.
Time frame: From Baseline to the end of Week 35
Number of adverse events
Time frame: From Baseline to Follow-up (Up to 37 weeks)
Change in QT intervals measured by 12-lead electrocardiagram test over time
The duration of QT intervals will be measured with a standard 12-lead electrocardiagram test.
Time frame: From Baseline to the end of Week 35
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PACT Kidney Care - Orange
Orange, Connecticut, United States
RECRUITINGUS Renal Care - Fort Myers South
Fort Myers, Florida, United States
RECRUITINGNephrology & Hypertension Specialists
Dalton, Georgia, United States
RECRUITINGRenal Associates Of Baton Rouge, LLC
Baton Rouge, Louisiana, United States
RECRUITINGNephrology Associates, P.C. - Columbus
Columbus, Mississippi, United States
RECRUITINGNephrology & Hypertension Associates Ltd - Tupelo
Tupelo, Mississippi, United States
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