ImCheck Provides Promising Updated Patient Response Data from the Phase I/IIa EVICTION Trial with ICT01 at SITC Meeting 2021

November 12, 2021

Marseille, France, November 12, 2021 – ImCheck Therapeutics provided updated patient response data from its ongoing EVICTION Phase I/IIa clinical trial of its lead candidate ICT01 in an oral presentation at the Society for Immunotherapy of Cancer (SITC) Meeting 2021. In efficacy evaluable patients (n=8) treated with the combination of low dose ICT01 plus pembrolizumab who previously failed at least one prior checkpoint inhibitor regimen, 62% showed disease control by RECIST1.1 criteria. Two patients demonstrated a preliminary positive durable response at 24 and 32 weeks. In one metastatic melanoma patient with a brain metastasis, which would typically be unresponsive to standard of care treatments, a complete response of the brain metastasis was observed at week 27 of treatment. ImCheck is presenting these updates in addition to two posters covering ICT01 at SITC. The conference is taking place in Washington, D.C. and virtually, from November 10 – 14, 2021.

“These latest data from the EVICTION trial support our confidence that ICT01 has significant potential to provide meaningful therapeutic effects, particularly in patients with advanced, metastatic solid tumors that did not respond to prior checkpoint inhibitor therapy,” commented Paul Frohna, MD, PhD, Chief Medical Officer at ImCheck Therapeutics.“Although the brain metastasis response needs replication in more patients, this provides a highly valuable, clinical development opportunity in a group of patients with high unmet medical need that we intend to explore further.”

In the oral presentation today, titled “Clinical Activity of ICT01, an anti-BTN3A-Targeted, γ9δ2-Activating mAb, Alone and in Combination with Pembrolizumab in Patients with Advanced/Refractory Solid Tumors: EVICTION Trial”, Prof. Martin Wermke, Early Clinical Trial Unit, University Hospital Carl Gustav Carus, Dresden, Germany, presentedresults demonstrating ICT01 plus pembrolizumab induced anti-tumor responses in patients with a range of solid tumors. Five of eight patients (bladder cancer, metastatic melanoma, non-small cell lung cancer (n=3)) achieved disease control at 8 weeks and beyond according to RECIST1.1, including two partial responses at week 16 and beyond.

In the poster presentation titled, “ICT01, an anti-BTN3A monoclonal antibody, and NL-201, an alpha-independent IL-2/IL-15 agonist, combine to elicit a potent anti-tumor response by synergistically stimulating Vγ9Vδ2 T cell activation and proliferation”, a preclinical study of ICT01 plus NL-201 treatment suggests favorable results from the synergistic activity of both candidates through enhanced γ9δ2 T cell activation, expansion and anti-tumor activity in comparison with monotherapy. The synergistic effect of this combined treatment makes a strong case for further investigation of this therapeutic approach.

The second poster, “Correlation of Baseline Circulating γ9δ2 T Cells Counts and Pharmacodynamic Activity of ICT01 in Cancer Patients: Preliminary Results from EVICTION and a Novel Patient Enrichment Strategy”, evaluated the relationship between the baseline number of circulating γ9δ2 T cells in patients and their response to ICT01 as an enrichment strategy that is being implemented in the monotherapy expansion arms of the EVICTION trial.

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