SOUTH SAN FRANCISCO, Calif., Nov. 07, 2022 (GLOBE NEWSWIRE) -- 23andMe Holding Co. (Nasdaq: ME) (“23andMe”), a leading human genetics and biopharmaceutical company with a mission to help people access, understand, and benefit from the human genome, is presenting a trials-in-progress poster detailing tumor types being evaluated in the expansion phase of its ongoing Phase 1 study for 23ME-00610, an investigational antibody targeting CD200R1 in patients with advanced solid malignancies, at the Society for Immunotherapy of Cancer’s (SITC) 37th Annual Meeting, November 8-12, 2022 in Boston, Massachusetts.
The poster includes details on how the monotherapy activity of 23ME-00610 will be evaluated in tumor indication-specific expansion cohorts (N~15/cohort), which include clear cell renal cell carcinoma; epithelial ovarian, fallopian tube or primary peritoneal carcinoma; neuroendocrine cancers including small cell lung cancer; and microsatellite instability-high (MSI-H) or tumor mutational burden-high (TMB-H) cancers that have progressed on standard therapies. A cohort of adolescents with locally advanced unresectable, or metastatic solid malignancies will also be enrolled.
The tumor indications for the expansion phase were selected based on pre-clinical and published data of the activity and expression of CD200R1 and its ligand, CD200, together with immune cell and tumor characteristics that have the potential to increase the likelihood of a response to CD200R1 inhibition.
23andMe has more than 13 million genotyped customers, over 80% of whom consent to participate in research. 23andMe scientists study the aggregate, de-identified genetics of these participants, alongside more than 4 billion self-reported health data points. Using these data and sophisticated bioinformatic analyses, 23andMe has discovered an immuno-oncology genetic signature to pinpoint areas of the genome that may harbor promising targets for cancer immunotherapies. One of these targets, CD200R1, is a receptor found predominantly on immune cells; by targeting this receptor, 23ME-00610 blocks CD200 on tumor cells from binding to CD200R1 on T-cells and myeloid cells, which may restore their ability to kill cancer cells.
“Our hypothesis, backed by published research, is that drug targets based on human genetics are more likely to prove successful than those with no underlying human genetic evidence,'' said Jennifer Low, MD, PhD, Head of Therapeutics Development at 23andMe. “We are testing if our antibody has activity in a variety of tumor types including those that traditionally don't respond to anti-PD(L)-1 treatment. We hope that 23ME-00610 will ultimately provide clinical benefit to patients with cancer.”
Poster Details
Title: A Phase 1 Dose Escalation and Expansion Study of the anti-CD200R1 Antibody 23ME-00610 in Patients with Advanced Solid Malignancies.
Session: Annual Meeting Regular Poster Abstract Presenter
Abstract/Poster Number: 758
Location: Hall C
Date and Time: Friday, November 11, 2022 - 9:00 a.m. – 8:30 p.m. ET
About 23ME-00610
23ME-00610 is a high-affinity humanized monoclonal antibody that is designed to bind to the CD200R1 receptor and prevent the interaction of CD200 and CD200R1. The CD200–CD200R1 axis is an immunological checkpoint that plays a pivotal role in maintenance of immune tolerance. CD200R1 is an inhibitory receptor expressed on T cells and myeloid cells while CD200, the ligand for CD200R1, is highly expressed on certain tumors. Binding of tumor associated CD200 to CD200R1 leads to immune suppression and decreased immune cell killing of cancer cells. Preclinical data indicate that this mechanism has the potential to restore the ability for both T-cells and myeloid cells to kill cancer cells.
The Phase 1 study is an open-label study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary clinical activity of 23ME-00610 in patients with advanced solid malignancies who have progressed on all available standard therapies. Clinical trials registry (clinicaltrials.gov): NCT05199272.
Reference, drug targets based on human genetics: Nelson et al., 2015 (Nature Genetics), King et al., 2019 (PLOS Genetics)
About 23andMe
23andMe is a genetics-led consumer healthcare and therapeutics company empowering a healthier future. For more information, please visit www.23andMe.com.
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