Zinplava(bezlotoxumab)
Zinplava (bezlotoxumab) is an antibody pharmaceutical. Bezlotoxumab was first approved as Zinplava on 2016-10-21. It is used to treat clostridium infections in the USA. It has been approved in Europe to treat pseudomembranous enterocolitis.
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Commercial
Trade Name
FDA
EMA
Zinplava
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Bezlotoxumab
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Zinplava | bezlotoxumab | Merck Sharp & Dohme | N-761046 RX | 2016-10-21 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
zinplava | Biologic Licensing Application | 2020-11-03 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
clostridium infections | EFO_1000874 | D003015 | A05.2 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
HCPCS
Code | Description |
---|---|
J0565 | Injection, bezlotoxumab, 10 mg |
Clinical
Clinical Trials
14 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Clostridium infections | D003015 | EFO_1000874 | A05.2 | — | 3 | 3 | 1 | 2 | 9 |
Recurrence | D012008 | — | 1 | — | 2 | 1 | 4 | ||
Inflammatory bowel diseases | D015212 | EFO_0003767 | — | 1 | — | 1 | — | 2 | |
Clostridioides difficile | D016360 | NCBITaxon_1496 | — | — | — | 2 | — | 2 | |
Ulcerative colitis | D003093 | EFO_0000729 | K51 | — | — | — | 1 | — | 1 |
Crohn disease | D003424 | EFO_0000384 | K50 | — | — | — | 1 | — | 1 |
Colitis | D003092 | EFO_0003872 | K52.9 | — | — | — | 1 | — | 1 |
Pseudomembranous enterocolitis | D004761 | EFO_1001314 | A04.7 | — | — | — | 1 | — | 1 |
Indications Phases 3
No data
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Mortality | D009026 | EFO_0004352 | — | 1 | — | — | — | 1 |
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | BEZLOTOXUMAB |
INN | bezlotoxumab |
Description | Bezlotoxumab (human mab) |
Classification | Antibody |
Drug class | monoclonal antibodies |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | >4NP4:H,I|bezlotoxumab heavy chain
EVQLVQSGAEVKKSGESLKISCKGSGYSFTSYWIGWVRQMPGKGLEWMGIFYPGDSSTRYSPSFQGQVTISADKSVNTAY
LQWSSLKASDTAMYYCARRRNWGNAFDIWGQGTMVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSW
NSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSC
>4NP4:L,M|bezlotoxumab light chain
EIVLTQSPGTLSLSPGERATLSCRASQSVSSSYLAWYQQKPGQAPRLLIYGASSRATGIPDRFSGSGSGTDFTLTISRLE
PEDFAVYYCQQYGSSTWTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNS
QESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC |
Identifiers
PDB | 4NP4 |
CAS-ID | 1246264-45-8 |
RxCUI | 1855048 |
ChEMBL ID | CHEMBL2108670 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB13140 |
UNII ID | 4H5YMK1H2E (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 643 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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95,515 adverse events reported
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