Assess the Safety and Efficacy of Nephoxil® in Subjects With End Stage Renal Disease (ESRD) on Dialysis

PHASE4CompletedINTERVENTIONAL
Enrollment

202

Participants

Timeline

Start Date

April 12, 2017

Primary Completion Date

December 31, 2018

Study Completion Date

May 31, 2019

Conditions
Kidney Failure, ChronicEnd-stage Renal DiseasePhosphorus Metabolism DisordersHyperphosphatemia
Interventions
DRUG

Ferric Citrate

Ferric citrate will be provided as a 500mg capsule. All intervention doses will be based on serum phosphorus levels.

Trial Locations (9)

10002

Division of Nephrology, Department of Internal Medicine, National Taiwan University Hospital, Taipei

11042

Division of Nephrology, Department of Internal Medicine, Taipei Medical University Hospital, Taipei

11101

Division of Nephrology, Department of Internal Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei

11217

Division of Nephrology, Department of Internal Medicine, Taipei Veterans General Hospital, Taipei

20401

Division of Nephrology, Department of Internal Medicine, Keelung Chang Gung Memorial Hospital, Keelung

22060

Division of Nephrology, Department of Internal Medicine, Far East Memorial Hospital, New Taipei City

40705

Division of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung

80756

Division of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung City

83301

Division of Nephrology, Department of Internal Medicine, Kaohsiung Chang-Gung Memorial Hospital, Kaohsiung City

Sponsors
All Listed Sponsors
lead

Panion & BF Biotech Inc.

INDUSTRY