Iron poisoning

disease
On this page

Also known as iron overloadiron toxicity

Summary

Iron poisoning (MONDO:0800385) is a disease and 90 clinical trials. Top therapeutic interventions include deferasirox, deferiprone, and deferoxamine. A subtype of heavy metal poisoning — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 90

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameiron poisoning
Mondo IDMONDO:0800385
Is cancer (heuristic)no

Also known as: iron overload · iron toxicity

Disease family

This is a subtype of heavy metal poisoning. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › poisoningheavy metal poisoningiron poisoning

Related subtypes (2): thallium poisoning, cesium poisoning

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 90.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified47
PHASE217
PHASE412
PHASE37
PHASE14
PHASE2/PHASE32
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00117507PHASE4COMPLETEDStudy for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
NCT00171301PHASE4COMPLETEDExtension Study of the Efficacy and Safety of Deferasirox Treatment in Beta-thalassemia Patients With Transfusional Hemosiderosis (Study Amended to 2-year Duration)
NCT00654589PHASE4COMPLETEDEfficacy and Safety of Oral Deferasirox (20 mg/kg/d) in Pts 3 to 6 Months After Allogeneic Hematopoietic Cell Transplantation Who Present With Iron Overload
NCT00800761PHASE4COMPLETEDIntensive Combined Chelation Therapy for Iron-Induced Cardiac Disease in Patients With Thalassemia Major
NCT01335035PHASE4COMPLETEDOpen-Label Single-Arm Pilot Study in Adult Allogeneic Hematopoietic Stem Cell Transplant Recipients With Transfusional Iron Overload
NCT01546415PHASE4COMPLETEDSafety and Efficacy of Desferasirox in Chinese Patients With Iron Overload and Aplastic Anemia
NCT02041299PHASE4TERMINATEDEfficacy and Safety of Ferriprox® in Patients With Sickle Cell Disease or Other Anemias
NCT02443545PHASE4TERMINATEDLong-term Safety and Efficacy of Ferriprox® in Iron Overloaded Patients With Sickle Cell Disease or Other Anemias
NCT03191201PHASE4TERMINATEDA Double Blind Randomised Placebo-controlled Trial to Assess the Role of Iron Repletion in Glucose Homeostasis.
NCT03372083PHASE4COMPLETEDSafety Study of Crushed Deferasirox Film Coated Tablets in Pediatric Patients With Transfusional Hemosiderosis
NCT03388385PHASE4UNKNOWNAcute Effects of Intravenous Iron on Oxidative Stress and Endothelial Dysfunction in Non-dialysis CKD
NCT03591575PHASE4COMPLETEDSafety and Efficacy of Early Treatment With Deferiprone in Infants and Young Children
NCT00529152PHASE3COMPLETEDSafety and Efficacy of Ferriprox™ (Deferiprone) Oral Solution in Iron Overloaded Pediatric Patients
NCT00980421PHASE3UNKNOWNSafety of Various Mode of Delivery of Iron Supplement on Iron Toxicity Markers in Preschool Children
NCT00999349PHASE2/PHASE3UNKNOWNTherapeutic Effects of Silymarin in Patients With B-thalassemia Major
NCT01045525PHASE3COMPLETEDPhlebotomy and Lifestyle and Diet Advices vs Lifestyle and Diet Advices Only in Patients With Dysmetabolic Liversiderosis
NCT01342705PHASE3TERMINATEDPhlebotomy and Risk of Hepatocellular Carcinoma in Patients With Compensated Alcoholic Cirrhosis
NCT01395199PHASE3COMPLETEDAmlodipine in the Prevention and Treatment of Iron Overload in Patients With Thalassemia Major
NCT01825512PHASE3COMPLETEDEfficacy/Safety Study of Deferiprone Compared to Deferasirox in Paediatric Patients
NCT02720536PHASE3COMPLETEDExtended Evaluation of Deferasirox Film-coated Tablet (FCT) Formulation
NCT04292314PHASE2/PHASE3COMPLETEDHydroxy Urea, Omega 3, Nigella Sativa,Honey on Oxidative Stress and Iron Chelation in Pediatric Major Thalassemia
NCT00000588PHASE2COMPLETEDChelation Therapy of Iron Overload With Pyridoxal Isonicotinoyl Hydrazone
NCT00000595PHASE2COMPLETEDEvaluation of Subcutaneous Desferrioxamine as Treatment for Transfusional Hemochromatosis
NCT00110266PHASE2COMPLETEDStudy of Deferasirox for Treatment of Transfusional Iron Overload in Myelodysplastic Patients
NCT00110617PHASE2COMPLETEDStudy of Deferasirox Relative to Subcutaneous Deferoxamine in Sickle Cell Disease Patients
NCT00138684PHASE2COMPLETEDCytochrome P450 2E1 and Iron Overload
NCT00395629PHASE1/PHASE2COMPLETEDSafety and Efficacy of Deferasirox (ICL670) in Patients With Iron Overload Resulting From Hereditary Hemochromatosis
NCT00447694PHASE2COMPLETEDCardiac T2* in Beta-thalassemia Patients on Deferasirox Treatment
NCT00602446PHASE2TERMINATEDDeferasirox in Treating Patients With Iron Overload After Undergoing a Donor Stem Cell Transplant
NCT00689182PHASE2COMPLETEDSafety and Efficacy of Iron Reduction by Phlebotomy
NCT00901199PHASE2COMPLETEDCombined Chelation Therapy in Patients With Transfusion Dependent Thalassemia and Iron Overload
NCT00907283PHASE2UNKNOWNFerrochelating Treatment in Patients Affected by Neurodegeneration With Brain Iron Accumulation (NBIA)
NCT01159067PHASE2TERMINATEDDeferasirox for Treating Patients Who Have Undergone Allogeneic Stem Cell Transplant and Have Iron Overload
NCT01740713PHASE2COMPLETEDPharmacokinetic Study of Deferiprone in Paediatric Patients
NCT01927913PHASE2WITHDRAWNTreatment of Iron Overload Requiring Chelation Therapy
NCT02164253PHASE2COMPLETEDFocal Accumulation of Iron in Cerebral Regions in Early ALS (Amyotrophic Lateral Sclerosis) Patients
NCT03801889PHASE2WITHDRAWNSP-420 in Subjects With Transfusion-dependent Beta-Thalassemia or Other Rare Anemias
NCT04614779PHASE2COMPLETEDLong-term Clinical Study of CN128 in Thalassemia Patients
NCT05355766PHASE2COMPLETEDLong-term Clinical Study of CN128 in Thalassemia With Sever Liver Iron Overloaded Patients
NCT00004982PHASE1COMPLETEDCombination Iron Chelation Therapy

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
DEFERASIROX418
DEFERIPRONE412
DEFEROXAMINE48
AMLODIPINE42
FERRIC CARBOXYMALTOSE41
HYDROXYUREA41
NIFEDIPINE41
ARGININE31
HONEY31
SILIBININ31
SILYBIN A31
SP-42023
DEFERITAZOLE21
CHEMBL463523406
CHEMBL530848501
SILYBIN B01
SILYMARIN01