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Drug intelligence / Profile preview
brentuximab vedotin + rifampicin
- Development stage
- Phase 1
- Lead developer
- Pfizer
- Modality
- Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
Brentuximab vedotin is an antibody-drug conjugate composed of a chimeric IgG1 antibody directed against CD30, covalently linked to the microtubule-disrupting agent monomethyl auristatin E (MMAE). It binds to CD30-expressing cells, is internalized, and releases MMAE intracellularly via proteolytic cleavage. This disrupts the microtubule network, causing cell cycle arrest and apoptosis in malignant cells. Brentuximab vedotin is primarily indicated for various types of lymphoma including classical Hodgkin lymphoma (cHL), systemic anaplastic large cell lymphoma (sALCL), primary cutaneous anaplastic large cell lymphoma, and CD30-expressing mycosis fungoides[1][2][3][4][5]. Rifampicin is a small molecule antibiotic that inhibits bacterial DNA-dependent RNA polymerase. It is used mainly for the treatment of tuberculosis and other mycobacterial infections.
- Brand names
- RifadinRimactane
02
Targets
RNAP (Bacterial dna-dependent RNA polymerase)CD30 (CD30 antigen)
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