Ferumoxytol
drugOn this page
Also known as CODE 7228CODE-7228FerahemeRIENSO
Summary
Ferumoxytol (CHEMBL1201867) is an approved unknown; indicated across 18 conditions including anemia and chronic kidney disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Unknown
- Indications: 18 conditions
- Clinical trials: 78
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1201867 |
| Name | Ferumoxytol |
| Type | Unknown |
| Max phase | 4 |
Also known as: CODE 7228, CODE-7228, Feraheme, Ferumoxytol, RIENSO, Rienso, FERUMOXYTOL
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
18 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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| anemia | 4 | MONDO:0002280 | EFO:0004272 |
| chronic kidney disease | 4 | MONDO:0005300 | EFO:0003884 |
| iron deficiency anemia | 3 | MONDO:0001356 | HP:0001891 |
| coronary artery disorder | 3 | MONDO:0005010 | EFO:0001645 |
| AIDS dementia complex | 2 | MONDO:0020689 | EFO:0002608 |
| non-small cell lung carcinoma | 2 | MONDO:0005233 | EFO:0003060 |
| glioblastoma | 2 | MONDO:0018177 | EFO:0000519 |
| nervous system disorder | 2 | MONDO:0005071 | EFO:0000618 |
| temporal lobe epilepsy | 2 | MONDO:0005115 | EFO:0000773 |
| lung carcinoma | 2 | MONDO:0005138 | EFO:0001071 |
| neoplasm | 1 | MONDO:0005070 | EFO:0000616 |
| multiple sclerosis | 1 | MONDO:0005301 | MONDO:0005301 |
| urinary bladder neoplasm | 0 | MONDO:0004987 | EFO:0000294 |
| chronic progressive multiple sclerosis | 0 | MONDO:0005284 | EFO:0003840 |
| interstitial cystitis | 0 | MONDO:0018301 | EFO:0008507 |
| secondary progressive multiple sclerosis | 0 | MONDO:0000450 | EFO:0008522 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 78.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 18 |
| PHASE2 | 15 |
| PHASE3 | 14 |
| PHASE1 | 11 |
| EARLY_PHASE1 | 9 |
| PHASE4 | 8 |
| PHASE1/PHASE2 | 2 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04278651 | PHASE4 | RECRUITING | Early Antenatal Support for Iron Deficiency Anemia |
| NCT01148745 | PHASE4 | COMPLETED | Iron Indices and Intravenous Ferumoxytol: Time to Steady State |
| NCT01227616 | PHASE4 | COMPLETED | Compare Efficacy/Safety of Repeat Doses of Ferumoxytol With Iron Sucrose in CKD Subjects With IDA and on Hemodialysis |
| NCT01942460 | PHASE4 | COMPLETED | Ferumoxytol for Iron-Deficiency Anemia in Chronic Kidney Disease and Peritoneal Dialysis Patients |
| NCT02752191 | PHASE4 | COMPLETED | Feraheme As An MRI Contrast Agent For Pediatric Congenital Heart Disease |
| NCT04080908 | PHASE4 | TERMINATED | Study to Assess Feasibility and Safety of Iron Repletion With Feraheme in Iron Deficient Patients With Durable Ventricular Assist Device Support |
| NCT04205266 | PHASE4 | UNKNOWN | IV Iron vs Oral Iron for Treatment of Anemia in Women With Abnormal Uterine Bleeding |
| NCT05515874 | PHASE4 | COMPLETED | Predicting Stroke Risk in ICAD With Novel MRI |
| NCT03619850 | PHASE3 | RECRUITING | A Study to Evaluate the Safety (Compared to Iron Sucrose), Efficacy and Pharmacokinetics of Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects With Chronic Kidney Disease (CKD) |
| NCT03893045 | PHASE3 | RECRUITING | A Study to Evaluate Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects |
| NCT04268849 | PHASE3 | RECRUITING | Trial of IV vs Oral Iron Treatment of Iron Deficiency Anemia in the Post-Operative Bariatric Surgical Patient |
| NCT07461948 | PHASE3 | RECRUITING | Advanced Imaging Techniques for Evaluating the Tumor Immune Microenvironment in Glioblastoma Patients |
| NCT01114139 | PHASE3 | COMPLETED | A Trial Comparing Ferumoxytol With Placebo for the Treatment of Iron Deficiency Anemia |
| NCT01114204 | PHASE3 | COMPLETED | A Trial Comparing Ferumoxytol With Iron Sucrose for the Treatment of Iron Deficiency Anemia |
| NCT01114217 | PHASE3 | COMPLETED | A Trial of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia |
| NCT01155375 | PHASE3 | TERMINATED | A Trial of Ferumoxytol for the Treatment of Iron Deficiency Anemia in Pediatric Participants With Chronic Kidney Disease |
| NCT01155388 | PHASE3 | TERMINATED | A Trial of Ferumoxytol for the Treatment of Iron Deficiency Anemia in Pediatric Participants With Nondialysis-Dependent Chronic Kidney Disease |
| NCT01264679 | PHASE3 | TERMINATED | A Trial of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia in Pediatric Participants With Chronic Kidney Disease |
| NCT02319278 | PHASE2/PHASE3 | COMPLETED | DEtection of Cellular Inflammation With FERumoxytol in the HEART |
| NCT02694978 | PHASE3 | COMPLETED | A Phase III Safety Study of Ferumoxytol Compared to Ferric Carboxymaltose for the Treatment of Iron Deficiency Anemia (IDA) |
| NCT02954510 | PHASE3 | UNKNOWN | Ferumoxytol-enhanced Magnetic Resonance Imaging |
| NCT03657433 | PHASE3 | COMPLETED | Intravenous Infusions of Ferumoxytol Compared to Oral Ferrous Sulfate for the Treatment of Anemia in Pregnancy |
| NCT06348524 | PHASE3 | TERMINATED | Ferumoxytol-enhanced Magnetic Resonance Imaging |
| NCT01542879 | PHASE1/PHASE2 | RECRUITING | Development of Radiation Free Whole Body Magnetic Resonance (MR) Imaging Technique for Staging Children With Cancer |
| NCT03270059 | PHASE2 | RECRUITING | Gadolinium and Ferumoxytol MRI in Diagnosing Patients With Abnormalities in the Central Nervous System |
| NCT05340465 | PHASE2 | RECRUITING | Darbe Plus IV Iron to Decrease Transfusions While Maintaining Iron Sufficiency in Preterm Infants |
| NCT06483061 | PHASE2 | RECRUITING | Enhanced MRI Imaging in Healthy Participants and Participants With Epilepsy |
| NCT07452250 | PHASE2 | RECRUITING | Ferumoxytol-enhanced Magnetic Resonance Venography in Patients With Venous Diseases |
| NCT00659126 | PHASE2 | TERMINATED | Ferumoxytol- and Gadolinium-Labeled MRI in Measuring Tumors Before or After Treatment in Patients With Primary or Metastatic Brain Tumors |
| NCT00659776 | PHASE2 | TERMINATED | MR, Histologic And EM Imaging Of Intravenous Ferumoxytol In Central Nervous System (CNS) Inflammation |
| NCT00707876 | PHASE2 | COMPLETED | Magnetic Resonance Angiography for Peripheral Arterial Disease (PAD) |
| NCT01052779 | PHASE2 | COMPLETED | A Trial Comparing Ferumoxytol to Iron Sucrose for the Treatment of Iron Deficiency Anemia in Adult Subjects With Chronic Kidney Disease |
| NCT01336803 | PHASE2 | COMPLETED | Differentiation of Bone Sarcomas and Osteomyelitis With Ferumoxytol-Enhanced MRI |
| NCT02141490 | PHASE2 | COMPLETED | Study of Ferumoxytol Enhanced MRI for Detecting Lymph Node Metastases in Prostate, Bladder, and Kidney Cancers |
| NCT02189889 | PHASE1/PHASE2 | TERMINATED | Active Preoperative Anemia Management in Patients Undergoing Cardiac Surgery |
| NCT02499354 | PHASE2 | COMPLETED | Pilot Study: Randomized, Placebo-controlled Comparator Trial of IV vs Oral Iron Treatment of RLS With IDA. (IVOR-IDA) |
| NCT02678767 | PHASE2 | COMPLETED | Ferumoxytol-enhanced Imaging and Mapping in neuroAIDS |
| NCT03234309 | PHASE2 | WITHDRAWN | Ferumoxytol in Magnetic Resonance Imaging of Pediatric Patients With Brain Tumors |
| NCT03325166 | PHASE2 | TERMINATED | Pembrolizumab and Magnetic Resonance Imaging With Ferumoxytol in Treating Patients With Non-small Cell Lung Cancer and Brain Metastases |
| NCT03347617 | PHASE2 | TERMINATED | Ferumoxytol MRI in Assessing Response to Pembrolizumab in Patients With Glioblastoma |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).