Drug intelligence / Profile preview

SCIO-469 + bortezomib

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Small Molecules
Administration
Oral, Intravenous, Subcutaneous
01

Overview

SCIO-469 (talmapimod) is an orally active, selective inhibitor of p38α mitogen-activated protein kinase (MAPK), which blocks the synthesis of proinflammatory cytokines such as IL-1β, PGE2, VEGF, MIP-1α and TNFα. This inhibition reduces multiple myeloma tumor growth and survival and can help overcome drug resistance[2][7]. Bortezomib is a small molecule proteasome inhibitor that blocks the 26S proteasome in cells, leading to accumulation of proteins within cancer cells and subsequent cell death. It is approved for use in multiple myeloma and mantle cell lymphoma[1]. The combination of SCIO-469 with bortezomib has been studied in relapsed or refractory multiple myeloma patients; clinical trials showed that this combination was well tolerated with some evidence of efficacy[2][5].

Brand names
Boruzu
Other names
talmapimod
02

Targets

PSMB5 (Proteasome subunit beta Type-5)RK (Ribokinase)

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