Taurolidine
Defencath (taurolidine) is a small molecule pharmaceutical. Taurolidine was first approved as Defencath on 2023-11-15.
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Events Timeline
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FDA approval date
EMA approval date
Patent expiration date
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
Combinations
Defencath
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| defencath | New Drug Application | 2025-09-29 |
Indications
FDA
EMA
Agency Specific
FDA
EMA
Expiration | Code | ||
|---|---|---|---|
HEPARIN SODIUM / TAUROLIDINE, DEFENCATH, CORMEDIX | |||
| 2033-11-15 | GAIN | ||
| 2028-11-15 | NCE | ||
HCPCS
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Clinical
Clinical Trials
30 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Catheter-related infections | D055499 | — | — | — | — | 1 | 1 | 1 | 3 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Sepsis | D018805 | EFO_0001420 | A41.9 | — | — | 1 | — | 1 | 2 |
| Infections | D007239 | EFO_0000544 | — | — | — | 1 | — | 1 | 2 |
| Communicable diseases | D003141 | — | — | — | — | 1 | — | 1 | 2 |
| Chronic kidney failure | D007676 | EFO_0003884 | N18.6 | — | — | 1 | — | — | 1 |
| Renal insufficiency | D051437 | — | N19 | — | — | 1 | — | — | 1 |
Indications Phases 2
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Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Taurolidine |
| INN | taurolidine |
| Description | Taurolidine is a thiadiazinane. |
| Classification | Small molecule |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | O=S1(=O)CCN(CN2CCS(=O)(=O)NC2)CN1 |
Identifiers
| PDB | — |
| CAS-ID | 19388-87-5 |
| RxCUI | — |
| ChEMBL ID | CHEMBL2105420 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB12473 |
| UNII ID | 8OBZ1M4V3V (ChemIDplus, GSRS) |
Target
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Variants
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Financial
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Trends
PubMed Central
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Additional graphs summarizing 739 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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15 adverse events reported
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