Flotetuzumab
Flotetuzumab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Trade Name
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Drug Products
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EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
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Indications
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Agency Specific
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Patent Expiration
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ATC Codes
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HCPCS
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Clinical
Clinical Trials
8 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Myeloid leukemia acute | D015470 | C92.0 | 2 | 1 | — | — | 1 | 4 | |
| Hematologic neoplasms | D019337 | 1 | 1 | — | — | — | 2 | ||
| Precursor cell lymphoblastic leukemia-lymphoma | D054198 | C91.0 | 1 | 1 | — | — | — | 2 | |
| Bcr-abl positive chronic myelogenous leukemia | D015464 | EFO_0000340 | 1 | 1 | — | — | — | 2 | |
| Hodgkin disease | D006689 | C81 | 1 | 1 | — | — | — | 2 | |
| Systemic mastocytosis | D034721 | C96.21 | 1 | 1 | — | — | — | 2 | |
| Hairy cell leukemia | D007943 | C91.4 | 1 | 1 | — | — | — | 2 | |
| Biphenotypic leukemia acute | D015456 | C95.0 | — | 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 | FLOTETUZUMAB |
| INN | flotetuzumab |
| Description | Flotetuzumab (INN; development code MGD006) is a bispecific antibody designed for the treatment of acute myeloid leukemia.
|
| Classification | Antibody |
| Drug class | monoclonal antibodies |
| Image (chem structure or protein) | |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL3990038 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | — |
| UNII ID | 0AHT0IC02G (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
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Additional graphs summarizing 215 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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2 adverse events reported
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