Drug intelligence / Profile preview

brentuximab vedotin + chidamide

Development stage
Unknown
Lead developer
First Affiliated Hospital of Soochow University
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

Brentuximab vedotin + chidamide is a combination therapy regimen being evaluated for the treatment of CD30-positive peripheral T-cell lymphoma (PTCL). The regimen consists of brentuximab vedotin, an antibody-drug conjugate (ADC) that targets CD30-expressing cells to deliver the cytotoxic microtubule-disrupting agent monomethyl auristatin E (MMAE), and chidamide (tucidinostat), an orally available, subtype-selective histone deacetylase (HDAC) inhibitor. Preclinical studies suggest that chidamide synergistically enhances the apoptotic effects of brentuximab vedotin. This specific combination is being studied by The First Affiliated Hospital of Soochow University as an induction and consolidation therapy, followed by chidamide maintenance, particularly for patients who are unfit for standard chemotherapy.

Other names
chidamide + brentuximab vedotintucidinostat + brentuximab vedotinbrentuximab vedotin plus chidamide
02

Targets

CD30 (CD30 antigen)HDAC10 (Histone Deacetylase 10)HDAC1 (Histone Deacetylase 1)TUBB (Tubulin (alpha and beta subunits))

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