Sulodexide
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Also known as SulodexidaVessel due f
Summary
Sulodexide (CHEMBL2108086) is a phase-3 clinical-stage unknown (ATC B01AB11); indicated across 9 conditions including thrombotic disease and chronic kidney disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Unknown
- ATC class: B01AB11
- Indications: 9 conditions
- Clinical trials: 16
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2108086 |
| Name | Sulodexide |
| Type | Unknown |
| Max phase | 3 |
| ATC | B01AB11 |
Also known as: Sulodexida, Sulodexide, Vessel due f, SULODEXIDE
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
9 indications (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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| thrombotic disease | 3 | MONDO:0000831 | HP:0004419 |
| chronic kidney disease | 3 | MONDO:0005300 | EFO:0003884 |
| diabetic kidney disease | 3 | MONDO:0005016 | EFO:0000401 |
| peripheral arterial disease | 3 | MONDO:0005386 | EFO:0004265 |
| venous thromboembolism | 3 | MONDO:0005399 | EFO:0004286 |
| diabetic retinopathy | 2 | MONDO:0005266 | EFO:0003770 |
| severe acute respiratory syndrome | 2 | MONDO:0005091 | MONDO:0100096 |
| membranoproliferative glomerulonephritis | 1 | MONDO:0002461 | MONDO:0019736 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 16.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 7 |
| PHASE4 | 4 |
| PHASE2 | 2 |
| PHASE2/PHASE3 | 1 |
| PHASE1 | 1 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00130312 | PHASE4 | TERMINATED | Effect of Sulodexide in Overt Diabetic Nephropathy |
| NCT02512601 | PHASE4 | TERMINATED | Prospective Evaluation of the QoL of Patients With PTS Who Receive Compression Therapy and Sulodexide |
| NCT03504566 | PHASE4 | WITHDRAWN | Rotation for Optimal Targeting of Albuminuria and Treatment Evaluation (ROTATE-2) |
| NCT05252923 | PHASE4 | TERMINATED | Endothelial Protection in Convalescent COVID-19 Patients |
| NCT04257487 | PHASE3 | RECRUITING | Sulodexide, VESSEL®, for the Prevention of Recurrent Venous Thromboembolism (The Jason Study) |
| NCT06982196 | PHASE3 | ENROLLING_BY_INVITATION | Sulodexide in Controlling the Recurrence of Psoriasis |
| NCT00130208 | PHASE3 | COMPLETED | Effect of Sulodexide in Early Diabetic Nephropathy |
| NCT00462202 | PHASE3 | TERMINATED | Open Label Tolerability and Safety Study of KRX-101 in Australia, New Zealand, and Hong Kong |
| NCT01000545 | PHASE3 | UNKNOWN | The Efficacy and Safety Study of Sulodexide in Filipino Diabetic Patients With Chronic Kidney Disease |
| NCT03370705 | PHASE3 | UNKNOWN | Endothelial Function Evaluation in Patients With PAOD Treated With Sulodexide + Conventional Treatment (CT) Vs CT Alone |
| NCT04483830 | PHASE2/PHASE3 | COMPLETED | Suloexide in the Treatment of Early Stages of COVID-19 |
| NCT05371925 | PHASE3 | COMPLETED | Endothelial Protection in Post COVID-19 Patients With Sulodexide |
| NCT01295775 | PHASE2 | COMPLETED | Diabetic Retinopathy Sulodexide Study |
| NCT02737670 | PHASE2 | COMPLETED | Sulodexide Efficacy in Chronic Idiopathic Subjective Tinnitus |
| NCT00583427 | PHASE1 | WITHDRAWN | Sulodexide Treatment in Patients With Dense Deposit Disease |
| NCT05654233 | Not specified | UNKNOWN | The Study of Reducing Adverse Effects After Radiofrequency Ablation Combined With Sclerotherapy |
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).