Ontuxizumab
Ontuxizumab is an antibody pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
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HCPCS
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Clinical
Clinical Trials
6 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Neoplasms | D009369 | C80 | 3 | — | — | — | — | 3 | |
Non-hodgkin lymphoma | D008228 | C85.9 | 1 | — | — | — | — | 1 | |
Extranodal nk-t-cell lymphoma | D054391 | C86.0 | 1 | — | — | — | — | 1 | |
Precursor cell lymphoblastic leukemia-lymphoma | D054198 | C91.0 | 1 | — | — | — | — | 1 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | — | — | — | — | 1 | |
Hodgkin disease | D006689 | C81 | 1 | — | — | — | — | 1 | |
B-cell lymphoma marginal zone | D018442 | C88.4 | 1 | — | — | — | — | 1 | |
Follicular lymphoma | D008224 | C82 | 1 | — | — | — | — | 1 | |
Mantle-cell lymphoma | D020522 | C83.1 | 1 | — | — | — | — | 1 | |
Waldenstrom macroglobulinemia | D008258 | C88.0 | 1 | — | — | — | — | 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 | ONTUXIZUMAB |
INN | ontuxizumab |
Description | Ontuxizumab (humanized mab) |
Classification | Antibody |
Drug class | monoclonal antibodies |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 946415-62-9 |
RxCUI | — |
ChEMBL ID | CHEMBL2364659 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB16270 |
UNII ID | 0M2XT000YC (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 58 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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