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A Long-term, Observational Study to Monitor Mortality, Bone-related Adverse Events and the Safety of Subjects Who Were Recruited Into Study SPD405-309
Patients enrolled in a previous study (SPD405-309), who were exposed to lanthanum carbonate (Fosrenol), were eligible to continue on any prescribed treatment for hyperphosphatemia, including lanthanum carbonate (Fosrenol), for an additional 5 years. Patients were being observed for any bone adverse events or other serious adverse events, as well as the collection of mortality data.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Imperial care Dialysis Center
Lynwood, California, United States
Barnett Research and Communications Medical Group
Torrance, California, United States
Western new England Renal & Transplant Associates
Springfield, Massachusetts, United States
Mercy Medical Center
Canton, Ohio, United States
Hypertension & Nephrology, Inc.
Providence, Rhode Island, United States
Nephrology Associates, PC
Nashville, Tennessee, United States
University of Vermont
Burlington, Vermont, United States
Nephrology Associates, PC
Richmond, Virginia, United States
Bad König, Hesse, Germany
KfH Zentrum
Aachen, Germany
Start Date
March 15, 2007
Primary Completion Date
August 31, 2010
Completion Date
August 31, 2010
Last Updated
July 13, 2021
34
ACTUAL participants
Lanthanum carbonate
DRUG
Lead Sponsor
Shire
NCT06933472
NCT05085275
Data Source & Attribution
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