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RecruitingNCT06933472

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

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
264 (estimated)
Sponsor
Alebund Pharmaceuticals · Industry
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGAP301Three times a day, administered orally with three meals at a daily dose level from 2.7g to 9.0g
DRUGAP301 Low DoseThree times a day, administered orally with three meals at a daily dose level from 0.075g to 0.25g

Timeline

Start date
2025-06-13
Primary completion
2026-06-20
Completion
2027-01-10
First posted
2025-04-18
Last updated
2026-01-29

Locations

42 sites across 2 countries: United States, China

Regulatory

Source: ClinicalTrials.gov record NCT06933472. Inclusion in this directory is not an endorsement.