Chronic Kidney Disease Clinical Trial
Official title:
A Two-Arm, Open-Label, Standard of Care Control Evaluation of Ferric Citrate for the Transition From Chronic Kidney Disease Stage 4/5 to Chronic Kidney Stage 5D
It is the investigators hypothesis that participants treated with Ferric Citrate (FC) during the non-dialysis CKD stage (4/5) with sufficient duration prior to initiating RRT, will result in improved biochemical control of anemia (Hb, TSAT) and mineral metabolism (P, FGF23) and furthermore, will result in a reduced need for ESA and intravenous iron. The investigators further hypothesize that effective treatment of anemia and mineral metabolism with FC in the pre-dialysis and transition period will result in improved physical functioning, reduced hospitalization and reduced total cost of care when compared to participants receiving contemporaneously provided standard of care therapy.
This is an up to 50 week, phase 3, clinical trial in patients with estimated glomerular
filtration rate (eGFR) ≤ 20 ml/min/1.73m2. It will be comprised of an up to 36-week
non-dialysis period (NDP), or until such time as subjects require renal replacement therapy
(RRT) with dialysis when they will immediately roll into a 12-week dialysis period (DP). The
study will consist of up to 16 clinic visits over a maximum period of 50 weeks. There will be
a screening period of up to 14 days after which subjects will be randomized into the NDP in a
2:1 ratio to receive either FC (n=150) or SOC (n=75). Each eligible participant will be
randomized to either fixed dose open-label ferric citrate (FC) or standard of care (SOC)
treatment. Participants randomized to SOC will receive care directed by their primary
nephrologist throughout the study duration with the only restriction being that they cannot
receive treatment with FC during the NDP or DP. Participants randomized to FC will receive it
throughout the study duration.
220 participants were screened to randomize 200 subjects 2:1 (FC:SOC) into the NDP. It is
anticipated that 35-45% of participants will reach the dialysis period (DP) during the 36
week follow up. Participants who initiate RRT with dialysis will enter the Dialysis Period
(DP) during which those participants previously assigned to ferric citrate will continue to
receive open-label ferric citrate and those previously assigned to SOC will receive
open-label, non-FC phosphate binders at the discretion of their treating physician. During
this period all participants will be treated to standard of care guidelines which suggest
that if serum phosphate is above the upper limit of normal (4.5 mg/dL), it should be reduced.
During the DP, dose of P binders, use of ESA, intravenous iron and blood transfusions will be
at the discretion of the primary treating nephrologist. Participants assigned to the SOC
treatment arm may not receive FC at any point during the study.
Only participants that begin permanent RRT with dialysis will be eligible to enter the 12
week DP. Participants that do not begin RRT after 9 months participation in the NDP will be
deemed to have reach the end of study and have end of study procedures performed.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05491642 -
A Study in Male and Female Participants (After Menopause) With Mild to Moderate High Blood Pressure to Learn How Safe the Study Treatment BAY3283142 is, How it Affects the Body and How it Moves Into, Through and Out of the Body After Taking Single and Multiple Doses
|
Phase 1 | |
Recruiting |
NCT06363097 -
Urinary Uromodulin, Dietary Sodium Intake and Ambulatory Blood Pressure in Patients With Chronic Kidney Disease
|
||
Terminated |
NCT04043026 -
The Effects of Renal Function and Atrial Fibrillation on Lipoproteins and Clot Structure/Function
|
||
Completed |
NCT05318014 -
Low-protein Formula Supplements in Chronic Kidney Disease
|
N/A | |
Active, not recruiting |
NCT06071065 -
Clinical Pharmacist Intervention on Medication Adherence and Clinical Outcomes in Chronic Kidney Disease Patients
|
N/A | |
Completed |
NCT02878317 -
Skin Autofluorescence as a Risk Marker in People Receiving Dialysis.
|
||
Not yet recruiting |
NCT06039254 -
Safety and Pharmacokinetics of HRS-1780 in Healthy Subjects and Subjects With Impaired Renal Function
|
Phase 1 | |
Recruiting |
NCT03160326 -
The QUALITY Vets Project: Muscle Quality and Kidney Disease
|
||
Completed |
NCT02756520 -
Observational Study on CKD Treatment With a Ketosteril Supplemented Protein-restricted Diet (Keto-024-CNI)
|
||
Completed |
NCT02836574 -
A Study of Renal Autologous Cell Therapy (REACT) in Type 2 Diabetics With Chronic Kidney Disease
|
Phase 2 | |
Completed |
NCT02896309 -
The Effect of Correction of Metabolic Acidosis in CKD on Intrarenal RAS Activity
|
N/A | |
Completed |
NCT02875886 -
DD-study: Diet or Diuretics for Salt-sensitivity in Chronic Kidney Disease
|
Phase 4 | |
Withdrawn |
NCT02885545 -
The Strategy to Prevent Hemorrhage Associated With Anticoagulation in Renal Disease Management (STOP HARM) Trial
|
Phase 4 | |
Completed |
NCT02888171 -
Impact of Ferric Citrate vs Ferrous Sulfate on Iron Parameters and Hemoglobin in Individuals With CKD and Iron Deficiency
|
N/A | |
Active, not recruiting |
NCT02483039 -
Nephrologist Follow-up Versus Usual Care After an Acute Kidney Injury Hospitalization
|
N/A | |
Terminated |
NCT02543177 -
Optimised Procedure in Patients With NSTEMI and CKD
|
N/A | |
Completed |
NCT02369549 -
Micro-Particle Curcumin for the Treatment of Chronic Kidney Disease
|
Phase 3 | |
Completed |
NCT02992548 -
Effect of Pravastatin on Erythrocyte Membrane Fatty Acid Contents in Patients With Chronic Kidney Disease
|
Phase 4 | |
Recruiting |
NCT02205944 -
Impact of Presurgical Exercise on Hemodialysis Fistula Outcomes
|
N/A | |
Active, not recruiting |
NCT02231138 -
Efficacy and Safety of Abelmoschus Manihot for Chronic Kidney Disease
|
Phase 4 |