Drug intelligence / Profile preview

perifosine + bortezomib

Development stage
Discontinued
Lead developer
Ceapro
Modality
Small Molecules
Administration
Oral, Intravenous, Subcutaneous
01

Overview

**Perifosine + bortezomib** is a combination of perifosine, a synthetic oral alkylphospholipid, and bortezomib, a proteasome inhibitor, investigated for the treatment of relapsed or refractory multiple myeloma. Perifosine inhibits signal transduction pathways including PI3K/Akt, and bortezomib inhibits the 26S proteasome, resulting in apoptosis of cancer cells. The combination showed promising activity and manageable toxicity in early phase studies in heavily pretreated multiple myeloma patients, but a phase 3 trial was discontinued early after interim analysis found no significant improvement in progression-free survival over bortezomib plus dexamethasone alone[1][3][5].

02

Targets

AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)PSMB1 (26S Proteasome (β1-Subunit))ERKCTNNB1 (Beta-catenin)JNK (Mitogen-activated protein kinase kinase kinase family)PSMB5 (Proteasome subunit beta Type-5)

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