Drug intelligence / Profile preview

intismeran autogene + pembrolizumab + enfortumab vedotin

Development stage
Unknown
Lead developer
Merck
Modality
Small Molecules, mRNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intramuscular (for Intismeran Autogene), Intravenous (for Pembrolizumab And Enfortumab Vedotin)
01

Overview

A combination investigational regimen composed of three agents: - **Intismeran autogene** (also known as V940, formerly mRNA-4157) is an individualized, patient-specific neoantigen therapy based on mRNA technology. It is designed to stimulate immune responses targeting patient-specific tumor neoantigens. - **Pembrolizumab** is a humanized monoclonal antibody that inhibits the programmed cell death protein 1 (PD-1) pathway, which enhances the immune system's ability to detect and attack tumor cells. - **Enfortumab vedotin** is an antibody-drug conjugate consisting of a monoclonal antibody directed against Nectin-4, a protein highly expressed on some tumor cells, conjugated to the microtubule-disrupting agent monomethyl auristatin E (MMAE). This combination is intended for use in certain high-risk or advanced cancers, including melanoma and potentially other solid tumors, to combine individualized tumor antigen vaccination, immune checkpoint inhibition, and direct tumor cell killing by ADCs[1][2][3][4][5][6].

Brand names
Padcev (for enfortumab vedotin)Keytruda (for pembrolizumab)
Other names
individualized neoantigen therapy (for intismeran autogene)
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TUBB (Tubulin (alpha and beta subunits))PVRL4 (Nectin cell adhesion molecule 4)Neoantigens (Patient-specific tumor neoantigen epitopes)

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