On May 29, 2019 Arcus Biosciences, Inc. (NYSE:RCUS), a clinical-stage biopharmaceutical company focused on creating innovative cancer immunotherapies, reported the Company will be presenting preliminary data from the ongoing Phase 1 dose-escalation trials of AB928, a potential best-in-class dual A2a/A2b receptor antagonist, in a poster session at the 2019 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting taking place in Chicago, IL, from May 31-June 4, 2019 (Press release, Arcus Biosciences, MAY 29, 2019, View Source [SID1234536666]).
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Poster presentation details
Abstract Title: AB928, a Novel Dual Adenosine Antagonist, Combined With Chemotherapy or AB122 (anti-PD-1) in Patients With Advanced Tumors: Preliminary Results From Ongoing Phase 1 Studies
Abstract Number: 2604
Session Information: Developmental Immunotherapy and Tumor Immunobiology
Date and Time: Saturday, June 1, 8:00 a.m. – 11:00 a.m. Central Time
Location: Hall A
A copy of the poster will be available on the "Publications" section of the Arcus website at www.arcusbio.com.
Conference call details
Arcus will host a conference call and live webcast on Tuesday, June 25, 2019, at 1:30 p.m. Pacific Time/4:30 p.m. Eastern Time to provide a mid-year update on its clinical and preclinical programs. Investors interested in listening to the conference call may do so by dialing (866) 211-3164 in the U.S. or (647) 689-6573 internationally, using Conference ID: 7163128. In addition, the live webcast and accompanying slides will be available on the "Investors" section of the Arcus website at www.arcusbio.com. Following the live webcast, a replay will be available on the Company’s website for approximately 30 days.
About AB928
AB928 is an orally bioavailable, highly potent antagonist of the adenosine 2a and 2b receptors. The activation of these receptors by adenosine interferes with the activity of key populations of immune cells and inhibits an optimal anti-tumor immune response. By blocking these receptors, AB928 has the potential to reverse adenosine-induced immune suppression within the tumor microenvironment. AB928 was designed specifically for the oncology setting, with a profile that includes potent activity in the presence of high concentrations of adenosine and a minimal shift in potency due to non-specific protein binding, both essential properties for efficacy in the tumor microenvironment. AB928 has other attractive features, including high penetration of tumor tissue and low penetration through the healthy blood-brain barrier. In a Phase 1 trial in healthy volunteers, AB928 has been shown to be safe and well tolerated and to have pharmacokinetic and pharmacodynamic profiles consistent with a once-daily dosing regimen.
About AB122
AB122 is a fully human IgG4 antibody that potently and selectively blocks PD-1. The biochemical, biological and preclinical properties of AB122 have been shown to be similar to those of the marketed anti-PD-1 antibodies nivolumab and pembrolizumab. AB122 is being evaluated in ongoing Phase 1/1b dose-escalation and dose-expansion trials evaluating AB122 in combination with AB928, a potential best-in-class dual A2a/A2b receptor antagonist, and in combination with AB154, a potential best-in-class anti-TIGIT antibody. In May 2019, Arcus announced a clinical development collaboration with Strata Oncology utilizing Strata’s precision drug development platform and proprietary biomarkers to evaluate AB122 in a basket trial including tumor types that generally have low levels of response to anti-PD-1 therapy. AB122 is also being evaluated in an ongoing Phase 1 dose-escalation trial assessing monotherapy dosing schedules. The Company expects AB122 to form the backbone of many of its intra-portfolio combinations.