4.6 Article

A Novel Pharmacodynamic Biomarker and Mechanistic Modeling Facilitate the Development of Tovetumab, a Monoclonal Antibody Directed Against Platelet-Derived Growth Factor Receptor Alpha, for Cancer Therapy

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AAPS JOURNAL
卷 23, 期 1, 页码 -

出版社

SPRINGER
DOI: 10.1208/s12248-020-00523-3

关键词

biomarker; dose; modeling; PKPD; tovetumab

资金

  1. AstraZeneca

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Tovetumab, a fully human IgG2 monoclonal antibody, specifically binds to human PDGFR alpha and blocks signal transduction. Studies show that tovetumab competes with PDGF-AA for binding, indirectly measuring receptor occupancy and providing a novel PD biomarker approach.
Tovetumab (MEDI-575) is a fully human IgG2 kappa monoclonal antibody that specifically binds to human platelet-derived growth factor receptor alpha (PDGFR alpha) and blocks receptor signal transduction by PDGF ligands. The affinity of tovetumab determined using surface plasmon resonance technology and flow cytometry demonstrated comparable binding affinity for human and monkey PDGFR alpha. In single and repeat-dose monkey pharmacokinetic-pharmacodynamic (PK-PD) studies, tovetumab administration resulted in dose-dependent elevation of circulating levels of PDGF-AA, a member of the PDGF ligand family, due to displacement of PDGF-AA from PDGFR alpha by tovetumab and subsequent blockade of PDGFR alpha-mediated PDGF-AA degradation. As such, PDGF-AA accumulation is an indirect measurement of receptor occupancy and is a novel PD biomarker for tovetumab. The nonlinear PK of tovetumab and dose-dependent increase in circulating PDGF-AA profiles were well described by a novel mechanistic model, in which tovetumab and PDGF-AA compete for the binding to PDGFR alpha. To facilitate translational simulation, the internalization half-lives of PDGF-AA and tovetumab upon binding to PDGFR alpha were determined using confocal imaging to be 14 +/- 4 min and 30 +/- 8 min, respectively. By incorporating PDGFR alpha internalization kinetics, the model not only predicted the target receptor occupancy by tovetumab, but also the biologically active agonistic ligand-receptor complex. This work described a novel PD biomarker approach applicable for anti-receptor therapeutics and the first mechanistic model to delineate the in vivo tri-molecular system of a drug, its target receptor, and a competing endogenous ligand, which collectively have been used for optimal dose recommendation supporting clinical development of tovetumab.

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