Drug intelligence / Profile preview

TAK-573 + bortezomib + dexamethasone

Development stage
Unknown
Lead developer
Takeda
Modality
Small Molecules, Peptide-Protein Conjugates → Peptide Conjugates → Peptides
Administration
Intravenous, Subcutaneous, Oral
01

Overview

TAK-573 + bortezomib + dexamethasone is a combination therapy under investigation for relapsed or refractory multiple myeloma. TAK-573 is an engineered fusion protein (peptide-Fc fusion) that fuses a proprietary recombinant IgG1 Fc fragment with a modified human interleukin-15 (IL-15) molecule. TAK-573 is designed to stimulate the immune system by specifically expanding and activating natural killer (NK) cells and CD8+ cytotoxic T-cells, while limiting activation of regulatory T-cells. Bortezomib is a first-in-class proteasome inhibitor that inhibits the 26S proteasome, leading to apoptosis in malignant plasma cells. Dexamethasone is a synthetic glucocorticoid used for its anti-inflammatory and immunosuppressant effects, which also induce apoptosis in lymphoid cells. The combination leverages direct antitumor effects of bortezomib and dexamethasone, plus immune-mediated cytotoxicity stimulated by TAK-573, for synergistic treatment of multiple myeloma[6].

02

Targets

IFNAR (Immune system modulation via type I interferon receptor)CD38 (Cluster of Differentiation 38)GR (Glucocorticoid receptor)PSMB5 (Proteasome subunit beta Type-5)

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