Bamlanivimab
Bamlanivimab is an antibody pharmaceutical. It is currently being investigated in clinical studies. It is known to target spike glycoprotein.
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Commercial
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
Brand Name | Status | Last Update |
|---|---|---|
| bamlanivimab | Use Authorization | 2022-01-24 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
|---|---|---|---|
| covid-19 | — | D000086382 | U07.1 |
Agency Specific
FDA
EMA
No data
Patent Expiration
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ATC Codes
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HCPCS
Code | Description |
|---|---|
| M0245 | Intravenous infusion, bamlanivimab and etesevimab, includes infusion and post administration monitoring |
| M0246 | Intravenous infusion, bamlanivimab and etesevimab, includes infusion and post administration monitoring in the home or residence; this includes a beneficiary's home that has been made provider based to the hospital during the covid 19 public health emergency |
| Q0245 | Injection, bamlanivimab and etesevimab, 2100 mg |
Clinical
Clinical Trials
16 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Covid-19 | D000086382 | U07.1 | 1 | 5 | 5 | 3 | 2 | 14 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Coronavirus | D017934 | — | 1 | 1 | — | — | 1 | ||
| Severe acute respiratory syndrome-related coronavirus | D045473 | NCBITaxon_227859 | — | — | 1 | — | — | 1 |
Indications Phases 2
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Healthy volunteers/patients | — | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | BAMLANIVIMAB |
| INN | bamlanivimab |
| Description | Bamlanivimab is a monoclonal antibody developed by AbCellera Biologics and Eli Lilly as a treatment for COVID-19. The medication was granted an emergency use authorization (EUA) by the US Food and Drug Administration (FDA) in November 2020, and the EUA was revoked in April 2021.
|
| Classification | Antibody |
| Drug class | monoclonal antibodies |
| Image (chem structure or protein) | |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | 2423943-37-5 |
| RxCUI | 2463114 |
| ChEMBL ID | CHEMBL4650379 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB15718 |
| UNII ID | 45I6OFJ8QH (ChemIDplus, GSRS) |
Target
Variants
Clinical Variant
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Financial
Bamlanivimab - Eli Lilly
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 2,604 documents
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Safety
Black-box Warning
Black-box warning for: Bamlanivimab
Adverse Events
Top Adverse Reactions
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4,582 adverse events reported
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