| Drug Name |
Ofatumumab |
| Drug ID |
BADD_D01596 |
| Description |
Ofatumumab is a novel anti-CD20 monoclonal antibody that targets B-cells. It is an IgG1κ human monoclonal antibody produced from a recombinant murine cell line (NS0) via transgenic mouse and hybridoma technology.[L12612] Ofatumumab works by recognizing antigens that are expressed on the tumour cells in certain cancers; however, the antigen is not tumour-specific and can also be found in normal B-cells.[A6921] Ofatumumab was first approved by the FDA in 2009.[L12771] It is used in the treatment of recurrent, progressive, or recurrent chronic lymphocytic leukemia (CLL) or CLL in treatment-naive patients in whom fludarabine-based therapy is considered inappropriate. Ofatumumab is used as monotherapy or in combination with other medications, depending on the patient profile and previous treatment history.[L12612] Although it has a similar molecular mechanism of action as [rituximab], another CD-20 monoclonal antibody used in the treatment of rheumatoid arthritis and B-cell non-Hodgkin's lymphoma, ofatumumab has a higher affinity towards CD20.[A6921]
Ofatumumab is available for intravenous administration and is marketed as Arzerra. In Phase III clinical trials consisting of subjects with relapsing forms of multiple sclerosis (RMS), subcutaneous administration of ofatumumab reduced the number of relapses and delayed disease progression. In February 2020, FDA and EMA approved Supplemental Biologics License Application (sBLA) and Marketing Authorization Application (MAA), respectively, for ofatumumab for the treatment of RMS in adults.[L12753] The FDA subsequently approved ofatumumab for the treatment of RMS on August 20, 2020.[L15581] The potential therapeutic use of ofatumumab in various lymphomas and rheumatoid arthritis has also been investigated.[A193053] |
| Indications and Usage |
Ofatumumab is indicated, in combination with [chlorambucil], for the treatment of previously untreated patients with chronic lymphocytic leukemia (CLL) for whom fludarabine-based therapy is considered inappropriate.[L12612]
In patients with recurrent or progressive CLL, ofatumumab is indicated for extended treatment of patients who are in complete or partial response after at least two lines of therapy for recurrent or progressive CLL.[L12612]
Ofatumumab is indicated for the treatment of patients with CLL refractory to [fludarabine] and [alemtuzumab].[L12612]
Ofatumumab is also indicated for the treatment of adult patients with relapsing forms of multiple sclerosis, including active secondary progressive disease, clinically isolated syndrome, and relapsing-remitting disease.[L15581] |
| Marketing Status |
approved |
| ATC Code |
L01FA02; L04AA52 |
| DrugBank ID |
DB06650
|
| KEGG ID |
D09314
|
| MeSH ID |
C527517
|
| PubChem ID |
Not Available
|
| TTD Drug ID |
D0Y8ZN
|
| NDC Product Code |
0078-0690; 67643-0016; 0078-1007; 0078-0669 |
| UNII |
M95KG522R0
|
| Synonyms |
ofatumumab | kesimpta | HUMAX-CD20 2F2 | HUMAX-CD20-2F2 | HUMAX-CD20, 2F2 | GSKI841157 | GSK-1841157 | arzerra |
