Last reviewed · How we verify

Bortezomib-Rituximab-Bendamustine

Fondazione Italiana Linfomi - ETS · Phase 2 active Small molecule

Bortezomib-Rituximab-Bendamustine is a combination of a proteasome inhibitor, a monoclonal antibody, and a chemotherapy agent.

Bortezomib-Rituximab-Bendamustine is a combination of a proteasome inhibitor, a monoclonal antibody, and a chemotherapy agent. Used for Relapsed or refractory mantle cell lymphoma.

At a glance

Generic nameBortezomib-Rituximab-Bendamustine
Also known asBRB
SponsorFondazione Italiana Linfomi - ETS
Drug classProteasome inhibitor, Monoclonal antibody, Chemotherapy agent
TargetCD20, Proteasome
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Bortezomib targets the proteasome, disrupting cell growth and survival. Rituximab targets CD20 on B cells, leading to their depletion. Bendamustine is a chemotherapy agent that interferes with DNA replication and repair.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: