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Bortezomib-Melphalan

University Hospital, Toulouse · Phase 3 active Small molecule

Bortezomib inhibits the proteasome to trigger cancer cell death, while melphalan is an alkylating agent that damages DNA in cancer cells.

Bortezomib inhibits the proteasome to trigger cancer cell death, while melphalan is an alkylating agent that damages DNA in cancer cells. Used for Multiple myeloma (induction therapy in phase 3 trials).

At a glance

Generic nameBortezomib-Melphalan
SponsorUniversity Hospital, Toulouse
Drug classProteasome inhibitor + alkylating agent combination
TargetProteasome (bortezomib); DNA (melphalan)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

This combination pairs bortezomib, a proteasome inhibitor that prevents degradation of pro-apoptotic proteins and causes accumulation of misfolded proteins in cancer cells, with melphalan, a nitrogen mustard alkylating agent that cross-links DNA and induces cell death. The combination is designed to enhance cytotoxicity in multiple myeloma and other hematologic malignancies through complementary mechanisms.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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