Drug intelligence / Profile preview

BV-CHEP

Development stage
Unknown
Lead developer
UNC Lineberger Comprehensive Cancer Center
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

BV-CHEP is an investigational combination chemotherapy regimen consisting of the antibody-drug conjugate brentuximab vedotin (Adcetris) and a chemotherapy backbone of cyclophosphamide, doxorubicin, etoposide, and prednisone (CHEP). Developed by the UNC Lineberger Comprehensive Cancer Center, this regimen is primarily evaluated for the treatment of aggressive adult T-cell leukemia/lymphoma (ATLL). Brentuximab vedotin targets CD30-expressing cancer cells to deliver the cytotoxic microtubule-disrupting agent monomethyl auristatin E (MMAE). The CHEP components provide multi-modal cytotoxic activity: cyclophosphamide acts as a DNA alkylating agent, doxorubicin as a DNA intercalator and topoisomerase II inhibitor, etoposide as a topoisomerase II inhibitor, and prednisone as a lympholytic corticosteroid. The regimen is administered in 21-day cycles and aims to improve remission rates in ATLL, a rare and often treatment-resistant malignancy.

Other names
Brentuximab Vedotin With Cyclophosphamide, Doxorubicin, Etoposide, and PrednisoneCHEP-UNC Lineberger Comprehensive Cancer Center-adult T-cell leukemia/lymphoma
02

Targets

DNAGR (Glucocorticoid receptor)TOP2A (DNA topoisomerase II)CD30 (CD30 antigen)TUBB (Tubulin (alpha and beta subunits))

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