PO.IM01.14 · 免疫学

Characterization and functional evaluation of PF-08634404 (SSGJ-707) a tetravalent PD-1 x VEGF bispecific for the treatment of cancer

海报缩略图:Characterization and functional evaluation of PF-08634404 (SSGJ-707) a tetravalent PD-1 x VEGF bispecific for the treatment of cancer
编号 5541 展板 13 时间 4/21 02:00–05:00 区域 Section 6 主讲 Ryan Heiser, PhD
分会场 Bi- and Tri-Specific Antibody Therapies
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作者与单位

Ryan A. Heiser1, Meghan Zuck1, Catalina Sakai1, Eliana Moskovitz1, Laila Shehata2, Markus Carlson1, Florian Heinkel1, Sherif Abdelhamed3, MIchelle Ulrich1, Matt Rathgeber1, Brian P. O'Connor1, Joseph D. Dekker1, Haomin Huang4, Sharsti Sandall1

1Pfizer Oncology, Bothell, WA,2Pfizer Oncology, Seattle, WA,3Pfizer Oncology, Bothell, Bothell, WA,43SBio Inc., Shanghai, China

摘要 Abstract

PF-08634404 (formerly known as SSGJ-707) is an investigational anti-PD-1 and anti-VEGF bispecific antibody designed to simultaneously inhibit PD-1-mediated T cell dysfunction and VEGF-A-mediated tumor angiogenesis and immune suppression in the tumor microenvironment. PF-08634404 is a tetravalent 2+2 bispecific leveraging Common Light Chain Linear Fab x2 (CLF 2 ) technology with an IgG4 backbone. The PD-1 and VEGF-A binding arms of PF-08634404 are unique among the PD-1 x VEGF bispecific class. PF-08634404 has demonstrated promising clinical activity in NSCLC and CRC in clinical trials conducted in China. Here we present preclinical data demonstrating binding to and functional inhibition of PD-1 and VEGF-A by PF-08634404 in vitro. PF-08634404 displays nanomolar binding affinities for PD-1 and VEGF-A and can bind both targets simultaneously. The functional inhibition of VEGF by PF-08634404 is increased (~7.5-fold) compared to relevant benchmarks, and the inhibition of PD-1 is equivalent or superior to relevant benchmarks. Consistent with this class of bispecific molecules, PF-08634400 multimerizes in the presence of dimeric VEGF-A, increasing the avidity for PD-1 (>100-fold), driving rapid internalization of PD-1 on T cells, and improving the functional inhibition of PD-1 (>10-fold). Collectively, these data characterize core features of the bispecific mechanism and support the ongoing clinical investigation of PF-08634404 proof of concept and pivotal trials in multiple disease settings/tumor types.
利益披露 Disclosure
R. A. Heiser, Pfizer Employment, Stock, Stock Option. M. Zuck, Pfizer Employment. M. Carlson, Pfizer Employment. F. Heinkel, Pfizer Employment. M. Ulrich, Pfizer Employment. M. Rathgeber, Pfizer Employment. J. D. Dekker, Pfizer Employment.

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