Cilgavimab
Evusheld (cilgavimab) is an antibody pharmaceutical. Cilgavimab was first approved as Evusheld on 2022-03-25. It is known to target spike glycoprotein.
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Clinical
Clinical Trials
12 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 |
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Covid-19 | D000086382 | U07.1 | — | 3 | 3 | — | 2 | 8 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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X-linked combined immunodeficiency diseases | D053632 | EFO_1001451 | — | 1 | — | — | — | 1 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Borna disease virus | D001891 | 1 | — | — | — | — | 1 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | CILGAVIMAB |
INN | cilgavimab |
Description | Tixagevimab/cilgavimab, sold under the brand name Evusheld, is a combination of two human monoclonal antibodies, tixagevimab (AZD8895) and cilgavimab (AZD1061) targeted against the surface spike protein of SARS-CoV-2 used to prevent COVID-19. It is being developed by British-Swedish multinational pharmaceutical and biotechnology company AstraZeneca. It is co-packaged and given as two separate consecutive intramuscular injections (one injection per monoclonal antibody, given in immediate succession).
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Classification | Antibody |
Drug class | monoclonal antibodies |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL4650258 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB16394 |
UNII ID | 1KUR4BN70F (ChemIDplus, GSRS) |
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Evusheld - AstraZeneca
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Safety
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0 adverse events reported
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