Drug intelligence / Profile preview

PF-07062119 (Pfizer)

Development stage
Discontinued
Lead developer
Pfizer
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

PF-07062119 is an antibody-drug conjugate (ADC) developed by Pfizer, comprising a humanized IgG1 monoclonal antibody directed against programmed cell death 1 ligand 1 (PD-L1) conjugated to the cytotoxic microtubule-disrupting agent monomethyl auristatin E (MMAE). The conjugation is achieved via a protease-cleavable valine-citrulline (vc) linker. PF-07062119 is designed to selectively bind to PD-L1-expressing tumor cells, leading to internalization of the ADC and subsequent lysosomal cleavage of the linker. This release of MMAE into the cytoplasm inhibits tubulin polymerization, resulting in cell cycle arrest and apoptosis. Beyond direct cytotoxicity, the targeting of PD-L1 may also interfere with the PD-1/PD-L1 signaling axis, potentially enhancing anti-tumor immune responses. Clinical development was focused on advanced solid tumors, including non-small cell lung cancer (NSCLC), but the program was terminated by the sponsor for strategic reasons.

Other names
anti-PD-L1-vcMMAE ADCanti-PD-L-1-vcMMAE ADCanti-PD-L 1-vcMMAE ADChumanized IgG1 anti-PD-L1 monoclonal antibody conjugated to monomethyl auristatin E via a valine-citrulline linker
02

Targets

CD3 (T-cell surface glycoprotein CD3)GUCY2C (Guanylate cyclase C receptor)

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