Sucralfate

drug
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Also known as Aluminum sucrose octasulfateAntepsinCarafateCitogelHexagastronKealSuccosaSucralfate hydrateSucralfatoSucralfinSucrateSugastSulcrateUlcarUlcerminUlcogantUlsanicUrbalVenter

Summary

Sucralfate (CHEMBL6067980) is an approved unknown (ATC A02BX02); indicated across 6 conditions including peptic ulcer disease and gastroesophageal reflux disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Unknown
  • ATC class: A02BX02
  • Indications: 6 conditions
  • Clinical trials: 17

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL6067980
NameSucralfate
TypeUnknown
Max phase4
ATCA02BX02

Also known as: Aluminum sucrose octasulfate, Antepsin, Carafate, Citogel, Hexagastron, Keal, Succosa, Sucralfate, Sucralfate hydrate, Sucralfato, Sucralfin, Sucrate

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

6 indications (3 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
peptic ulcer disease4MONDO:0004247HP:0004398
gastroesophageal reflux disease4MONDO:0007186EFO:0003948
duodenal ulcer4MONDO:0005412EFO:0004607
esophagitis2MONDO:0001409HP:0100633
eosinophilic esophagitis0MONDO:0005361EFO:0004232

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

Clinical trials

Total trials: 17.

Phase distribution

PhaseTrials
PHASE47
Not specified3
PHASE22
PHASE31
PHASE2/PHASE31
PHASE1/PHASE21
EARLY_PHASE11
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07257926PHASE4NOT_YET_RECRUITINGPrevention of Delayed Post-polypectomy Bleeding by Endoscopic Sucralfate Spray in High-risk Patients: A Randomized Controlled Trial
NCT07312370PHASE4NOT_YET_RECRUITINGEsomeprazole Plus Sucralfate for Post-ESD Ulcer Healing
NCT07611162PHASE4NOT_YET_RECRUITINGComparative Effectiveness of Alginate, Magaldrate, Sucralfate, Proton Pump Inhibitors, and Diet in Laryngopharyngeal Reflux Disease
NCT00702871PHASE4COMPLETEDA Clinico-Bacteriological Study and Effect of Stress Ulcer Prophylaxis on Occurrence of Ventilator Associated Pneumonia
NCT01284647PHASE4COMPLETEDA Study to Evaluate the Efficacy of Teprenone On Chinese Patients With Chronic Non-Atrophic Erosive Gastritis
NCT01613534PHASE4COMPLETEDCombined Therapy in Radiation Proctopathy
NCT03635372PHASE4COMPLETEDA Comparison of Effectiveness of Oral Sucrolfate, Alginate and Hydrotalcide in Dispeptic Pain Treatment
NCT05369234PHASE3COMPLETEDEffects of Oral Aloe Vera Juice on Chemotherapy and Radiation-induced Oral Mucositis and Esophagitis
NCT07310927PHASE2/PHASE3COMPLETEDAlginate vs Sucralfate for GERD Symptomatic Relief
NCT05659576PHASE2ACTIVE_NOT_RECRUITINGReducing Acute Upper Gastrointestinal Side-Effects of Thoracic Irradiation
NCT03241030PHASE2COMPLETEDSucralfate to Improve Oral Intake in Children With Infectious Oral Ulcers: a Randomized, Double-blind, Placebo-Controlled Trial
NCT06617026PHASE1/PHASE2COMPLETEDShort-Term Outcome of Medical Vs. Surgical Management Of Chronic Anal Fissure
NCT05817656PHASE1UNKNOWNColonoscopic Sucralfate Spray in Prevention of Delayed Polypectomy Bleeding
NCT02353078EARLY_PHASE1COMPLETEDThe Effect of Sucralfate Slurry in Patients With Eosinophilic Esophagitis
NCT06107504Not specifiedRECRUITINGPrevention of Post-sphincterotomy Bleeding
NCT02039869Not specifiedWITHDRAWNConfocal Endomicroscopy for Non-Erosive Reflux Disease (CE NERD)
NCT02788591Not specifiedTERMINATEDConfocal Endomicroscopy for Non-Erosive Reflux Disease Detection

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).