briumvi
briumvi: developed by 1 company · 1 FDA decision.
briumvi evidence translation
What we can confirm
1 FDA record
What it means
What to watch
Prepared research question
How could briumvi → TGTX affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence1 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (1)
| Company | Phase |
|---|---|
| TG THERAPEUTICS, INC. (TGTX) Relapsing forms of multiple sclerosis (RMS), to include clin… | Approved |
FDA Decisions1 records
Frequently asked questions
Who is developing briumvi?
briumvi is being developed by TG THERAPEUTICS, INC..
What is briumvi's latest FDA decision?
The most recent tracked FDA decision for briumvi is Approval for 1 INDICATIONS AND USAGE BRIUMVI is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. BRIUMVI is a CD20-directed cytolytic antibody indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults ( 1 , 14 )., dated December 28, 2022.