Thrombomodulin alfa
Thrombomodulin alfa is a protein pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
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Clinical
Clinical Trials
8 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Disseminated intravascular coagulation | D004211 | HP_0005521 | D65 | — | 1 | — | 1 | — | 2 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Sepsis | D018805 | HP_0100806 | A41.9 | — | 1 | 2 | — | — | 3 |
| Toxemia | D014115 | — | — | — | 1 | 2 | — | — | 3 |
| Blood coagulation disorders | D001778 | EFO_0009314 | D68.9 | — | — | 2 | — | — | 2 |
| Hemostatic disorders | D020141 | — | — | — | — | 2 | — | — | 2 |
| Fibrosis | D005355 | — | — | — | — | 1 | — | — | 1 |
| Idiopathic pulmonary fibrosis | D054990 | — | J84.112 | — | — | 1 | — | — | 1 |
| Pulmonary fibrosis | D011658 | — | — | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Peripheral nervous system diseases | D010523 | HP_0009830 | G64 | 1 | 1 | — | — | — | 2 |
| Colonic neoplasms | D003110 | — | C18 | — | 1 | — | — | — | 1 |
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 | Thrombomodulin alfa |
| INN | thrombomodulin alfa |
| Description | Thrombomodulin alfa |
| Classification | Protein |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL2108653 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | — |
| UNII ID | 2VU8WT49WX (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 247 documents
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Safety
Black-box Warning
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Adverse Events
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84 adverse events reported
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