Calcium Acetate

drug
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Also known as Acetic acidcalcium saltAcetic acid, calcium salt (2:1)Calcarea aceticaCalcium acetate anhydrousCalcium acetate component of procalamineanhydrousE-263E263EliphosEveroseFEMA NO. 2228INS NO.263INS-263PhosexPhosloPhoslo gelcapsPhoslyraRenacet

Summary

Calcium Acetate (CHEMBL1200800) is an approved small-molecule chelator (ATC V03AE07); indicated across 5 conditions including hyperphosphatemia and chronic kidney disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: V03AE07
  • Indications: 5 conditions
  • Clinical trials: 10
  • Chemistry: 158.17 Da · C4H6CaO4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1200800
NameCalcium Acetate
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID6116
ChEBICHEBI:3310
ATCV03AE07
Molecular formulaC4H6CaO4
Molecular weight158.17
InChIKeyVSGNNIFQASZAOI-UHFFFAOYSA-L

SMILES: CC(=O)[O-].CC(=O)[O-].[Ca+2]

IUPAC name: calcium diacetate

ChEBI definition: The calcium salt of acetic acid. It is used, commonly as a hydrate, to treat hyperphosphataemia (excess phosphate in the blood) in patients with kidney disease: the calcium ion combines with dietary phosphate to form (insoluble) calcium phosphate, which is excreted in the faeces.

Pharmacological roles (ChEBI): chelator.

Also known as: Acetic acid, calcium salt, Acetic acid, calcium salt (2:1), Calcarea acetica, Calcium acetate, Calcium acetate anhydrous, Calcium acetate component of procalamine, anhydrous, E-263, E263, Eliphos, Everose

Patent coverage: 24,840 distinct patent families (64,576 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

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

5 indications (4 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
hyperphosphatemia4MONDO:0000328HP:0002905
chronic kidney disease4MONDO:0005300EFO:0003884
kidney failure4MONDO:0001106EFO:1002048

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

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE43
Not specified3
PHASE31
PHASE21
EARLY_PHASE11
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00211939PHASE4COMPLETEDCARE-2 (Calcium Acetate [PhosLo®]/Sevelamer[Renagel®] Evaluation Study 2) for Heart Calcification in Dialysis Patients
NCT01135615PHASE4COMPLETEDSevelamer, FGF-23 and Endothelial Dysfunction in Chronic Kidney Disease (CKD)
NCT01277497PHASE4TERMINATEDEffect of Phosphate Binders on Markers of Vascular Health in Chronic Kidney Disease Stages 3 and 4
NCT00211978PHASE3COMPLETEDEPIC(Effect of PhosLo on Phosphorus Levels in Chronic Kidney Disease)
NCT05424263PHASE2UNKNOWNAcetate and Age-associated Arterial Dysfunction
NCT04299633PHASE1COMPLETEDStudy in Healthy Adult Subjects to Assess the Effect of Phosphate Binders on the Pharmacokinetics of a Single Dose of Vadadustat
NCT01991574EARLY_PHASE1COMPLETEDEffect of the Consumption of Ferric Hydroxide Adipate on Urinary Phosphorus Excretion.
NCT00018135Not specifiedCOMPLETEDParathyroid Hormone Levels in Relation to the Phosphorus Content of Meals
NCT00364000Not specifiedWITHDRAWNArterial Stiffness and Calcifications in Haemodialysis Patients on Sevelamer or Calcium Acetate
NCT00785629Not specifiedCOMPLETEDA Double Blind Randomized Placebo Trial of Maintenance of Normal Serum Phosphorus in CKD

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

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