Anthracycline
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Clinical
Clinical Trials
2836 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Breast neoplasms | D001943 | EFO_0003869 | C50 | — | 13 | 5 | — | — | 18 |
| Lymphoma | D008223 | — | C85.9 | 4 | 10 | 2 | — | — | 13 |
| Non-hodgkin lymphoma | D008228 | — | C85.9 | 2 | 4 | 1 | — | — | 6 |
| Follicular lymphoma | D008224 | — | C82 | — | — | 2 | — | — | 2 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| B-cell lymphoma | D016393 | — | — | 4 | 8 | — | — | — | 10 |
| Large b-cell lymphoma diffuse | D016403 | — | C83.3 | 4 | 6 | — | — | — | 8 |
| Myeloid leukemia acute | D015470 | — | C92.0 | 2 | 1 | — | — | — | 2 |
| Osteosarcoma | D012516 | — | — | — | 1 | — | — | — | 1 |
| Benign fibrous histiocytoma | D018219 | — | — | — | 1 | — | — | — | 1 |
| Histiocytoma | D051642 | — | — | — | 1 | — | — | — | 1 |
| Malignant fibrous histiocytoma | D051677 | — | — | — | 1 | — | — | — | 1 |
| Triple negative breast neoplasms | D064726 | — | — | — | 1 | — | — | — | 1 |
| B-cell chronic lymphocytic leukemia | D015451 | — | C91.1 | — | 1 | — | — | — | 1 |
| Reactive arthritis | D016918 | EFO_0007460 | M02.3 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Aggression | D000374 | EFO_0003015 | — | 1 | — | — | — | — | 1 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | — |
| INN | — |
| Description | — |
| Classification | Unknown |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | — |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | — |
| UNII ID | — |
Target
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89 adverse events reported
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