Loncastuximab
Zynlonta (loncastuximab) is an antibody pharmaceutical. Loncastuximab was first approved as Zynlonta on 2022-12-20. It has been approved in Europe to treat b-cell lymphoma and large b-cell lymphoma diffuse. It is known to target B-lymphocyte antigen CD19.
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Commercial
Trade Name
FDA
EMA
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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
FDA
EMA
Brand Name | Status | Last Update |
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zynlonta | Biologic Licensing Application | 2022-10-19 |
Indications
FDA
EMA
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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
Code | Description |
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C9084 | Injection, loncastuximab tesirine-lpyl, 0.1 mg |
Clinical
Clinical Trials
24 clinical trials
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Indications Phases 4
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Follicular lymphoma | D008224 | C82 | 2 | 4 | — | — | — | 6 | |
Mantle-cell lymphoma | D020522 | C83.1 | 3 | 3 | — | — | — | 5 | |
Non-hodgkin lymphoma | D008228 | C85.9 | 3 | 1 | — | — | — | 4 | |
B-cell lymphoma | D016393 | 2 | 2 | — | — | — | 4 | ||
Lymphoma | D008223 | C85.9 | 1 | 1 | — | — | — | 2 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | 1 | — | — | — | 2 | |
Waldenstrom macroglobulinemia | D008258 | C88.0 | 1 | 1 | — | — | — | 2 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | LONCASTUXIMAB |
INN | loncastuximab |
Description | Loncastuximab tesirine, sold under the brand name Zynlonta, is a monoclonal antibody conjugate medication used to treat large B-cell lymphoma and high-grade B-cell lymphoma. It is an antibody-drug conjugate (ADC) composed of a humanized antibody targeting the protein CD19.
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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 | 1879918-31-6 |
RxCUI | — |
ChEMBL ID | CHEMBL4297238 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB16222 |
UNII ID | NYM5HO7I39 (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
Variants
Clinical Variant
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Trends
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Additional graphs summarizing 250 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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3 adverse events reported
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