Ocrevus/ocrelizumab vs Briumvi
both anti-CD20 antibodies reviewed for relapsing multiple sclerosis
Ocrevus/ocrelizumab
Roche Holding AG ยท 1620 cited findings โ
Briumvi(ublituximab-xiiy)
TG THERAPEUTICS, INC ยท 1744 cited findings โ
What the regulatory reviews say
Ocrevus (ocrelizumab) is indicated for the treatment of patients with relapsing forms of multiple sclerosis (RMS). Regulators reviewed its efficacy, noting a 46% relapse rate reduction compared to Rebif in its pivotal trials. Briumvi (ublituximab-xiiy) is indicated for the treatment of relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. Its review highlighted an Annualized Relapse Rate (ARR) of 0.09 in its own studies.
These drugs were evaluated in separate clinical trials with distinct designs, patient populations, and timepoints. Ocrevus's review cited a relapse rate of 0.16 for ocrelizumab compared to 0.29 for Rebif. Briumvi's review reported an ARR of 0.09 for ublituximab-xiiy versus 0.23 for its comparator. The trials utilized different comparators and assessed various endpoints.
It is crucial to understand that the figures presented for Ocrevus and Briumvi are derived from independent studies and are not directly comparable. These trials had different designs, patient populations, and timepoints, and therefore, no direct comparison or implication of superiority between the two drugs can be made based on these figures.
Each drug's own results โ cited
| Ocrevus/ocrelizumab | Briumvi | |
|---|---|---|
| Relapse Rate (Drug) | 0.16 Ocrelizumab Roche Holding AG โ Ocrevus FDA Review (BLA761053, ORIG 1, 20, p.198 | 0.09 Annualized Relapse Rate (ARR) TG THERAPEUTICS, INC โ Briumvi FDA Review (BLA761238, ORIG 1, p.52 |
| Relapse Rate (Comparator) | 0.29 Rebif Roche Holding AG โ Ocrevus FDA Review (BLA761053, ORIG 1, 20, p.198 | 0.23 Annualized Relapse Rate (ARR) comparator TG THERAPEUTICS, INC โ Briumvi FDA Review (BLA761238, ORIG 1, p.52 |
| Infusion Related Reactions (IRRs) | 35 incidence in all MS trials pool Roche Holding AG โ Ocrevus FDA Review (BLA761053, ORIG 1, 20, p.265 | 2.8 CTCAE Grade 3 or higher IRRs in ublituximab-xiiy TG THERAPEUTICS, INC โ Briumvi FDA Review (BLA761238, ORIG 1, p.201 |
Explore the full evidence
Every cited finding behind both drugs is in the Neurology research library โ
Figures are as stated in the cited regulatory review documents. Educational reference only โ not medical or investment advice.