Continuous Soluble Ferric Pyrophosphate (SFP) Iron Delivery Via Dialysate in Hemodialysis Patients

Stage 1: Main Inclusion Criteria:

• Adult subject ≥ 18 years of age undergoing chronic hemodialysis three or four timesper week for chronic kidney disease (CKD) for at least 4 months, and expected toremain on hemodialysis three to four times weekly and be able to complete the durationof the study.

• Received IV iron therapy between 6 months and 2 weeks prior to enrollment in order toreplace iron losses resulting from hemodialysis procedure.

• Mean Screening Hgb ≥ 9.5 to ≤ 11.5 grams per deciliter (g/dL).

• Mean Screening Transferrin Saturation (TSAT) ≥ 15% to ≤ 40%.

• Mean Screening serum ferritin ≥ 200 to ≤ 800 micrograms per liter (µg/L).

• If being administered epoetin, darbepoetin, or CERA, epoetin dose ≤ 45,000 Units (U)/week, darbepoetin dose ≤ 200 micrograms (µg)/week, or CERA dose ≤ 400 micrograms (µg)/month during the four weeks prior to enrollment.

Main Exclusion Criteria:

• Patient has living kidney donor identified or living-donor kidney transplantscheduled. (Note: Patients awaiting deceased-donor transplant need not be excluded.)

• Vascular access for dialysis with femoral catheter or non-tunneled catheter.

• Received a total of > 800 milligrams (mg) IV iron during the 8 weeks prior toenrollment

• If being administered an ESA, route of administration change or ESA dose change > 35% (i.e., [max - min dose]/max dose > 0.35) over the 2 weeks prior to screening.

• Serum albumin < 3.0 grams per deciliter (g/dL) any time over the 8 weeks prior toenrollment.

• Red Blood Cell (RBC) or whole blood transfusion within 12 weeks prior to enrollment. Stage 2: Main Inclusion Criteria:

• Patient currently enrolled in the Stage 1 run-in period of study.

• Undergoing chronic hemodialysis three or four times per week for chronic kidneydisease (CKD), and expected to remain on hemodialysis three to four times weekly andbe able to complete duration of the study.

• Mean Hgb ≥ 9.5 to ≤ 11.5 g/dL over the three most recent consecutive every-weekmeasurements prior to randomization.

• Stable Hgb defined as ≤ 1.0 g/dL difference between the maximum and minimum Hgb valuesover the 3 weeks immediately prior to randomization.

• Mean TSAT ≥ 15% to ≤ 40% over the two most recent consecutive every-other-weekmeasurements prior to randomization.

• Mean serum ferritin ≥ 200 to ≤ 800 µg/L over the two most recent consecutiveevery-other-week measurements prior to randomization.

• If being administered epoetin, darbepoetin, or CERA, epoetin dose ≤ 45,000 U/week,darbepoetin dose ≤ 200 µg/week, or CERA dose ≤ 400 µg/month during the four weeksprior to randomization. Main Exclusion Criteria:

• Patient has living kidney donor identified or living-donor kidney transplantscheduled. (Note: Patients awaiting deceased-donor transplant need not be excluded.)

• Vascular access for dialysis with femoral catheter or non-tunneled catheter.

• Received any amount of IV iron during the 4 weeks prior to randomization.

• If being administered an (Erythropoietin Stimulating Agent) ESA, change in dose overthe 6 weeks immediately prior to randomization.

• Serum albumin < 3.0 g/dL any time over the 8 weeks prior to randomization.

• RBC or whole blood transfusion during Stage 1. Stage 3: Main Inclusion Criteria:

• Patient randomized in Stage 2 who has completed the full duration of Stage 2 and lessthan 4 weeks have elapsed since completion of Stage 2, OR

• Patient in Stage 2 who has been prematurely withdrawn from Stage 2 forprotocol-defined Protocol-Mandated Change in Anemia Management and less than 4 weekshave elapsed since withdrawal from Stage 2, OR

• Patient in Stage 2 who has been prematurely withdrawn from Stage 2 for Hgb >11.5 g/dLover ≥ 1 week confirmed by ≥ 2 consecutive measurements AND an associated increase inHgb by ≥ 1 g/dL over 4 weeks. Main Exclusion Criteria:

• Patient in Stage 2 who has been prematurely withdrawn from Stage 2 for any reasonother than as noted in inclusion criteria above.