Drug profile · INN
glofitamab-gxbm
COLUMVI
glofitamab-gxbm (COLUMVI) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.
Drug details — glofitamab-gxbm
- US status
- approved
- Class
- —
- Route
- INJECTION
- Patents
- 0
- Programs
- 3
- Data quality
- 0.84
Quick answer
glofitamab-gxbm (COLUMVI) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.
Key facts
Mechanism of action
B-lymphocyte antigen CD20 binding agent
Primary target: B-lymphocyte antigen CD20
Approval history
| Authority | Status | Date |
|---|---|---|
| FDA | approved | — |
Pipeline programs
Related & competitor drugs
Frequently asked questions
What is glofitamab-gxbm?
glofitamab-gxbm (COLUMVI) is a b-lymphocyte antigen cd20 binding agent. Route of administration: injection. Current US regulatory status: approved.
What is the brand name for glofitamab-gxbm?
COLUMVI is a marketed brand name for glofitamab-gxbm. Check FDA Drugs@FDA for the current US label holder and prescribing information.
What is the US approval status of glofitamab-gxbm?
glofitamab-gxbm has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.