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Anemia of Chronic Kidney Disease clinical trials

View clinical trials related to Anemia of Chronic Kidney Disease.

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NCT ID: NCT02581124 Completed - Clinical trials for Anemia of Chronic Kidney Disease

Study to Evaluate Effect of Lapatinib on Pharmacokinetics of JTZ-951 in Subjects With End-stage Renal Disease

Start date: October 2015
Phase: Phase 1
Study type: Interventional

Study to evaluate the effect of lapatinib, a breast cancer resistance protein (BCRP) inhibitor, on the pharmacokinetics (PK) of JTZ-951 and to evaluate the safety and tolerability of JTZ-951 when administered alone and one hour after the administration of lapatinib.

NCT ID: NCT02268994 Completed - Clinical trials for Anemia of Chronic Kidney Disease

KRX-0502 (Ferric Citrate) for the Treatment of IDA in Adult Subjects With NDD-CKD

Start date: October 2014
Phase: Phase 3
Study type: Interventional

a 24-week phase 3, multi-center clinical trial, comprised of a 16-week, randomized, double-blind, placebo-controlled period ("Randomized Period"), followed by an 8-week open-label safety extension period, where all subjects receive KRX-0502 (ferric citrate) ("Extension Period").

NCT ID: NCT02198495 Completed - Clinical trials for Anemia of Chronic Kidney Disease

Comparison Study of Two Iron Compounds for Treatment of Anemia in Hemodialysis Patients

COPEFER
Start date: September 2014
Phase: Phase 4
Study type: Interventional

Patients with end-stage kidney disease on maintenance hemodialysis frequently require iron supplementation to compensate for ongoing iron losses, and to maintain hemoglobin levels with or without additional use of erythropoiesis-stimulating agents (ESA). The investigators aim to compare two different intravenous iron preparations, ferric carboxymaltose and iron sucrose in 140 hemodialysis patients. The investigators primary objective is to assess whether both agents are equally effective to maintain a target haemoglobin within 10-12 mg/dl. The investigators will also measure ferritin, transferrin, transferrin saturation, and how much ESA therapy is administered. Patients will be randomly assigned to either treatment group and followed in parallel over an active study period of 40 weeks.

NCT ID: NCT02128074 Completed - Clinical trials for Anemia of Chronic Kidney Disease

A Pilot Study of KRX-0502 (Ferric Citrate, Administered Without Food, in Treating Iron-deficiency Anemia

Start date: April 2014
Phase: Phase 2
Study type: Interventional

The objective of the study is to evaluate the efficacy and safety of KRX-0502, administered without food, in treating iron deficiency anemia in subjects with stage 3 to 5 non-dialysis dependent chronic kidney disease (NDD-CKD).

NCT ID: NCT01971164 Completed - Clinical trials for Anemia of Chronic Kidney Disease

Safety, Tolerability, PK & PD Study of JTZ-951 in Anemic Subjects With End-stage Renal Disease

Start date: May 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of sequential ascending doses of JTZ-951 administered for 15 days in anemic subjects with end-stage renal disease (ESRD) receiving hemodialysis.

NCT ID: NCT01532349 Recruiting - Clinical trials for Anemia of Chronic Kidney Disease

Vitamin D as a Modifier of Serum Hepcidin in Children With Chronic Kidney Disease

D-fense
Start date: May 2012
Phase: Phase 2
Study type: Interventional

This research is being done to study the effectiveness of vitamin D (cholecalciferol) to modify hepcidin levels in children with chronic kidney disease (CKD). Anemia is a common problem in children with CKD. Anemia is when the body does not have enough healthy red blood cells. Hepcidin is a protein in the blood which interferes with the body's production of red blood cells. This study will see if vitamin D lowers hepcidin levels in children and young adults with CKD. If so, it could be used as an additional treatment for anemia in these children, in addition to the current therapies already in use including iron supplements and erythropoietin. People between the ages of 1 and 21 with CKD may be considered for this study.