The primary objective of this study is to demonstrate the long-term safety and tolerability of MCI-196 in the subjects with stage V chronic kidney disease on dialysis with hyperphosphatemia. The secondary objective of this study is to assess the long-term efficacy of flexible doses of MCI-196.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
116
3g to 15g/day (3 times a day), Tablet, 52 weeks of flexible dose
Unnamed facility
Los Angeles, California, United States
Unnamed facility
Orange, California, United States
Unnamed facility
Number of Adverse Events (AE)
Time frame: 52 weeks
The Change in Serum Phosphorus From Baseline to Week 52
Time frame: 52 weeks
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Tarzana, California, United States
Unnamed facility
Orlando, Florida, United States
Unnamed facility
Pembroke Pines, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Gurnee, Illinois, United States
Unnamed facility
Evansville, Indiana, United States
Unnamed facility
Baton Rouge, Louisiana, United States
Unnamed facility
New Orleans, Louisiana, United States
...and 11 more locations