Ferrous Ascorbate

drug
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Also known as AscoferCompleferIron(ii) ascorbateJ290.062IL-ascorbic acidiron complexNedifer

Summary

Ferrous Ascorbate (CHEMBL3707305) is a phase-3 clinical-stage small molecule (ATC B03AA10); indicated across 1 condition including anemia.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: B03AA10
  • Indications: 1 condition
  • Clinical trials: 3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3707305
NameFerrous Ascorbate
TypeSmall molecule
Max phase3
ATCB03AA10

Also known as: Ascofer, Complefer, Ferrous ascorbate, Iron(ii) ascorbate, J290.062I, L-ascorbic acid, iron complex, Nedifer, FERROUS ASCORBATE

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

1 indication (0 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
anemia3MONDO:0002280EFO:0004272

Clinical trials

Total trials: 3.

Phase distribution

PhaseTrials
PHASE32
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01160198PHASE3COMPLETEDA Study to Demonstrate the Efficacy and Tolerability of Ferrous Bisglycinate Chelate in Iron Deficiency Anaemia and to Compare These With Those of Ferrous Ascorbate.
NCT05957328PHASE3UNKNOWNA Study to Compare Liposomal Iron With Ferrous Ascorbate in the Treatment of Iron Deficiency Anemia in Children
NCT06303531Not specifiedUNKNOWNEfficacious Iron for Iron Deficiency Anemia in Adults Aged ≥18 Years

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).