Daunorubicin hydrochloride
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Commercial
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Clinical
Clinical Trials
470 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 |
|---|---|---|---|---|---|---|---|---|---|
| Myeloid leukemia acute | D015470 | — | C92.0 | 11 | 13 | 2 | — | — | 23 |
| Leukemia | D007938 | — | C95 | 9 | 11 | 1 | — | — | 20 |
| Myeloid leukemia | D007951 | — | C92 | 9 | 8 | 2 | — | — | 17 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Myelodysplastic syndromes | D009190 | — | D46 | 4 | 3 | — | — | — | 7 |
| Precursor cell lymphoblastic leukemia-lymphoma | D054198 | — | — | 2 | 4 | — | — | — | 6 |
| Neoplasms | D009369 | — | C80 | 2 | 4 | — | — | — | 5 |
| Preleukemia | D011289 | — | — | 2 | 1 | — | — | — | 3 |
| Eyelid neoplasms | D005142 | EFO_1000934 | — | — | 3 | — | — | — | 3 |
| Lymphoid leukemia | D007945 | — | C91 | — | 3 | — | — | — | 3 |
| Neoplasm metastasis | D009362 | EFO_0009708 | — | — | 1 | — | — | 1 | 2 |
| Non-hodgkin lymphoma | D008228 | — | C85.9 | 1 | 1 | — | — | — | 2 |
| Lymphoma | D008223 | — | C85.9 | 1 | 1 | — | — | — | 2 |
| Myeloproliferative disorders | D009196 | — | D47.1 | 1 | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Syndrome | D013577 | — | — | 2 | — | — | — | — | 2 |
| Hematologic neoplasms | D019337 | — | — | 2 | — | — | — | — | 2 |
| Hodgkin disease | D006689 | — | C81 | 1 | — | — | — | — | 1 |
| Large b-cell lymphoma diffuse | D016403 | — | C83.3 | 1 | — | — | — | — | 1 |
| Large-cell lymphoma anaplastic | D017728 | — | C84.6 | 1 | — | — | — | — | 1 |
| Burkitt lymphoma | D002051 | — | C83.7 | 1 | — | — | — | — | 1 |
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Epidemiology
Epidemiological information for investigational and approved indications
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Additional graphs summarizing 286 documents
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Safety
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Adverse Events
Top Adverse Reactions
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1,285 adverse events reported
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