Fumaric Acid

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Also known as Allomaleic-acidBoletic-acidE-297E297FEMA NO. 2488Fumaricum acidumINS NO.297INS-297NSC-2752fumarateSID17389670SID85148759SID69355ACIDE_FUMARIQUESID144213143SID144208967

Summary

Fumaric Acid (CHEMBL503160) is a phase-3 clinical-stage small-molecule geroprotector (ATC D05AX01); indicated across 2 conditions including psoriasis and cutaneous lupus erythematosus.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: D05AX01
  • Indications: 2 conditions
  • Clinical trials: 11
  • Chemistry: 116.07 Da · C4H4O4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL503160
NameFumaric Acid
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID444972
ChEBICHEBI:18012
ATCD05AX01
Molecular formulaC4H4O4
Molecular weight116.07
InChIKeyVZCYOOQTPOCHFL-OWOJBTEDSA-N

SMILES: C(=C/C(=O)O)\C(=O)O

IUPAC name: (E)-but-2-enedioic acid

ChEBI definition: A butenedioic acid in which the C=C double bond has E geometry. It is an intermediate metabolite in the citric acid cycle.

Pharmacological roles (ChEBI): geroprotector.

Other ChEBI roles (chemical / environmental): food acidity regulator, fundamental metabolite.

Also known as: Allomaleic-acid, Boletic-acid, E-297, E297, FEMA NO. 2488, Fumaric acid, Fumaricum acidum, INS NO.297, INS-297, NSC-2752, fumarate, fumaric acid

Patent coverage: 268,451 distinct patent families (845,433 SureChEMBL compound mentions), from 4 matched compound structure(s). One matched structure accounts for 844,402 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 3 (assay-derived). Sample: Thyrotropin receptor, Egl nine homolog 1, Prolyl hydroxylase EGLN3.

Bioactivity

ChEMBL activities: 2 potent at pChembl ≥ 5 of 5 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
TSHR5.4Potency3981nMCHEMBL_ACT_3917992
TSHR5.4Potency3981nMCHEMBL_ACT_4691130

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
psoriasis4MONDO:0005083EFO:0000676
cutaneous lupus erythematosus2MONDO:0005282EFO:0003834

Clinical trials

Total trials: 11.

Phase distribution

PhaseTrials
PHASE14
Not specified3
PHASE42
PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01996124PHASE4COMPLETEDAcute Effect of Pulmonary Desufflation on Cardiac Performance in COPD Patients
NCT05403047PHASE4UNKNOWNEfficacy of Tenofovir Disoproxil on Mother-to-child Transmission of HBV in Tokombéré, Cameroon in Pregnant Women
NCT02474082PHASE3COMPLETEDStudy of Secukinumab Compared to Fumaderm® in Adults With Moderate to Severe Psoriasis.
NCT06122454PHASE1/PHASE2UNKNOWNA Phase Ic/IIb Study to Evaluate the Efficacy,Safety and Pharmacokinetics of HST in Patients With CHB
NCT07538973PHASE1NOT_YET_RECRUITINGA Clinical Study to Evaluate the Pharmacokinetics and Safety of Anecatibin Fumarate Capsules in Subjects With Impaired Liver Function Versus Normal Liver Function
NCT00004886PHASE1COMPLETEDMS 209 Plus Docetaxel in Treating Patients With Advanced Solid Tumors
NCT01322451PHASE1COMPLETEDOral Bioavailability of Two Solid Formulations of GLPG0259.
NCT04309526PHASE1COMPLETEDSafety, Tolerability and Pharmacokinetics of NCO-48 Fumarate in Healthy Subjects
NCT06481787Not specifiedNOT_YET_RECRUITINGZuojin Wan Combined With Woonosan Fumarate for the Treatment of GRD Combined With Depression
NCT00631722Not specifiedCOMPLETEDMulticenter, Open-Label, Randomised, Haloperidol-controlled Study to Evaluate Seroquel as Mono-Therapy in the Treatment of Agitated Symptoms in the Patients With Acute Episode of Schizophrenia
NCT01812954Not specifiedCOMPLETEDEconomic Evaluation of Systemic Treatments for Moderate-to-severe Psoriasis

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).