772 A phase 1/2 dose escalation/expansion study evaluating the safety, pharmacokinetics, pharmacodynamics, and antitumor activity of E-602, a bi-sialidase fusion protein, in advanced cancer (GLIMMER-01)
Document Type
Presentation
Publication Date
11-8-2022
Keywords
oregon; chiles
Abstract
Background E-602 is a novel, first-in-class fusion protein of engineered human sialidases, neuraminidase (Neu)2, and the human IgG1 Fc region. The sialidase moieties of E-602 cleave terminal sialic acid residues from sialoglycans on diverse immune cell subsets and tumor cells. Sialoglycans are immunosuppressive in cancer, associated with poorer outcomes across numerous tumor indications, and have emerged as a critical glyco-immune checkpoint. In preclinical studies, sialidase-mediated cleavage of terminal sialic acids improves antitumor immunity by restoring the immune function of exhausted-like T cells and enhancing dendritic cell priming and naïve T cell activation.1 In multiple syngeneic mouse tumor models, sialidase treatment has demonstrated antitumor activity as monotherapy1 and additive antitumor activity when combined with anti-programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) blockade. E-602 has a wide safety margin, is not an immune agonist and does not stimulate cytokine activation in an in vitro PBMC cytokine release assay.1,2 In humans, E-602, via desialylation of tumor cells and immune cells, is expected to have antitumor activity either as monotherapy or in combination with an anti-PD-1 agent. Methods A Phase 1/2, first-in-human, open label, dose escalation and expansion study of E-602 administered as monotherapy and in combination with an anti-PD-1 agent is ongoing to evaluate the safety, pharmacokinetics, pharmacodynamics, and antitumor activity in participants with advanced cancers. Phase 1 of the study consists of 4 planned dose escalation cohorts of E-602 monotherapy and 2 planned dose escalation cohorts of E-602 in combination with an anti-PD-1 agent. Phase 1 is treating eligible participants with advanced melanoma, ovarian, non-small cell lung, colorectal, pancreatic, breast, gastric/esophagogastric junction, head and neck, or urothelial cancers. Utilizing a modified 3+3 study design in Phase 1, the safety of the dose regimens is under evaluation to identify the maximum tolerated dose and/or recommended Phase 2 dose. Additional participants (backfill) may be enrolled in the Phase 1 cohorts to obtain additional safety, pharmacokinetic or pharmacodynamic data. Phase 2 will include up to 3 disease indications, evaluating E-602 as monotherapy and/or in combination with an anti-PD-1 agent utilizing a Simon’s minimax 2-stage design. Pre and on-treatment biopsies to further explore the pharmacodynamic effects of E-602 are required for the Phase 1 backfill and Phase 2 participants. Acknowledgements The authors would like to thank the clinical trial participants and their families for their willingness to participate in the study. Trial Registration The study is registered on clinicaltrials.gov as NCT05259696. References Peng L, Cao L, Nerle S, et al. Development and engineering of human sialidase for degradation of immunosuppressive sialoglycans to treat cancer. J Immunother Cancer. 2021;9(Suppl 2):A1–A1054. Cao L, Che J, Chesney A, et al. Assessment of the safety, pharmacokinetics, and pharmacodynamics of a first-in-class cancer drug candidate E-602, a sialoglycan degrader, in non-human primates [abstracts]. Cancer Res. 2022;82(12_Suppl):abstracts nr LB203. Ethics Approval The study is approved by the Advarra institutional Ethics Board, approval number Pro00058627 and participants gave informed consent before taking part.
Area of Special Interest
Cancer
Specialty/Research Institute
Oncology
Specialty/Research Institute
Earle A. Chiles Research Institute
Comments
Presented at the SITC Annual Meeting; November 8-12; Boston, MA Authors: Manish Sharma1, Deanne Lathers2, Melissa Johnson3, Jason Luke4, Igor Puzanov5, Brendan Curti6, Christopher Chen7, Anthony El-Khoueiry8, Brian Henick9, Margaret Callahan10, Mario Sznol11, Sandip Patel12, Dawn Wilson2, Melissa Ricker2, Lizhi Cao2, Pushpa Jayaraman2, Jenny Che2, Li Peng2, David Feltquate2, Deanne Lathers2 and Anthony Tolcher13