Sodium Zirconium Cyclosilicate

drug
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Also known as LokelmaUXSi-9ZSZS-9

Summary

Sodium Zirconium Cyclosilicate (CHEMBL3301592) is an approved small molecule (ATC V03AE10); indicated across 2 conditions including heart failure.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: V03AE10
  • Indications: 2 conditions
  • Clinical trials: 20

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3301592
NameSodium Zirconium Cyclosilicate
TypeSmall molecule
Max phase4
ATCV03AE10

Also known as: Lokelma, Sodium zirconium cyclosilicate, UXSi-9, ZS, ZS-9, SODIUM ZIRCONIUM CYCLOSILICATE

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
heart failure2MONDO:0005252EFO:0003144

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 20.

Phase distribution

PhaseTrials
PHASE310
PHASE45
PHASE23
PHASE11
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04063930PHASE4UNKNOWNThe Effect of Sodium Zirconium Cyclosilicate on Albuminuria in Patients With Type 2 Diabetes and Hyperkalemia
NCT04585542PHASE4TERMINATEDComparison of Potassium Binders in the ER
NCT04676646PHASE4COMPLETEDStudy to Assess Efficacy and Safety of SZC for the Management of High Potassium in Patients With Symptomatic HFrEF Receiving Spironolactone
NCT05535920PHASE4COMPLETEDA Prospective, Randomized, Open-Label, Cross-Over Study of Lokelma to Control Interdialytic Hyperkalemia
NCT06365684PHASE4UNKNOWNSodium Zirconium Cyclosilicate to Allow Liberal Fruit and Vegetable Intake for Patients With CKD Stage 3b and 4
NCT06578078PHASE3RECRUITINGA Clinical Trial to Define the Best Strategy for the Management of Heart Failure in Elderly Patients
NCT06578533PHASE3RECRUITINGKeeping RAASi Treatment With Optimal Potassium Control
NCT02088073PHASE3COMPLETEDSafety & Efficacy of Zirconium Silicate Dosed for 28 Days in Hyperkalemia.
NCT02107092PHASE3COMPLETEDOpen-label Safety & Efficacy of ZS (Sodium Zirconium Cyclosilicate)10g qd to Extend Study ZS-004 in Hyperkalemia.
NCT02163499PHASE3COMPLETEDOpen-label Safety and Efficacy of Sodium Zirconium Cyclosilicate for up to 12 Months
NCT03528681PHASE3COMPLETEDA Study to Investigate the Safety and Efficacy of ZS in Patients With Hyperkalemia.
NCT04217590PHASE3COMPLETEDReduce Incidence of Pre-Dialysis Hyperkalaemia With Sodium Zirconium Cyclosilicate in Chinese Subjects
NCT04727528PHASE3TERMINATEDStudy of the Effect of SZC on Serum Potassium and Serum Bicarbonate in Patients With Hyperkalemia and Metabolic Acidosis Associated With Chronic Kidney Disease
NCT05004363PHASE3COMPLETEDLokelma for RAAS Maximisation in CKD & Heart Failure.
NCT05382988PHASE3COMPLETEDSodium Zirconium Cyclosilicate Lowers Hyperkalemia After Parathyroidectomy
NCT04789239PHASE2ACTIVE_NOT_RECRUITINGOPtimizing Aldosterone Receptor Antagonist Therapy by Sodium Zirconium Cyclosilicate in Heart Failure
NCT03532009PHASE2TERMINATEDPotassium Reduction Initiative to Optimize RAAS Inhibition Therapy With Sodium Zirconium Cyclosilicate in Heart Failure
NCT04983979PHASE2TERMINATEDThe ORTIZ Study: Optimising RASi Therapy With SZC
NCT04788641PHASE1COMPLETEDStudy to Assess the Effect of Sodium Zirconium Cyclosilicate on the Pharmacokinetics of Tacrolimus and Cyclosporin in Healthy Subjects
NCT04207203Not specifiedCOMPLETEDHealthy Diet Rich in Potassium to Chronic Kidney Disease With Sodium Zirconium Cyclosilicate: A Feasibility Study

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.