Monoclonal antibody | |
---|---|
Type | Whole antibody |
Source | Human |
Target | PD-L1 |
Clinical data | |
Trade names | Bavencio |
Other names | MSB0010718C |
AHFS/Drugs.com | Monograph |
MedlinePlus | a617006 |
License data | |
Pregnancy category |
|
Routes of administration | Intravenous infusion |
ATC code | |
Legal status | |
Legal status | |
Pharmacokinetic data | |
Metabolism | Proteolysis |
Elimination half-life | 6.1 days |
Identifiers | |
CAS Number | |
DrugBank | |
ChemSpider |
|
UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6374H9898N1694O2010S44 |
Molar mass | 143831.79 g·mol−1 |
Avelumab, sold under the brand name Bavencio, is a fully human monoclonal antibody medication for the treatment of Merkel cell carcinoma, urothelial carcinoma, and renal cell carcinoma.[5]
Common side effects include fatigue, musculoskeletal pain, diarrhea, nausea, infusion-related reactions, rash, decreased appetite and swelling of the limbs (peripheral edema).[7]
Avelumab targets the protein programmed death-ligand 1 (PD-L1). It has received orphan drug designation by the European Medicines Agency (EMA) for the treatment of gastric cancer in January 2017.[8] The US Food and Drug Administration (FDA) approved it in March 2017, for the treatment of Merkel-cell carcinoma,[7] an aggressive type of skin cancer. The EMA approved it in September 2017, for the same indication.[9] This is the first FDA-approved treatment for metastatic Merkel-cell carcinoma, a rare, aggressive form of skin cancer.[7] Avelumab was developed by Merck KGaA and Pfizer.[10]
FDA PR 20170323
was invoked but never defined (see the help page).