Northwire Canada EditionThursday, July 16, 2026
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HWY 0.370 +0.0% FCI 0.350 −7.9% GGAU 0.180 −5.3% KIRO 0.650 +1.6% LBNK 0.430 +0.0% BARU 0.040 +0.0% VCU 1.08 −5.3% NOBL 0.100 +0.0% SHL 0.355 +0.0% MTS 0.130 +0.0% FYL 0.090 +0.0% NUAG 5.42 −0.6% CAM 0.330 −1.5% SYH 0.398 −1.9% LOT 0.040 +0.0% CPL 0.210 +10.5% HWY 0.370 +0.0% FCI 0.350 −7.9% GGAU 0.180 −5.3% KIRO 0.650 +1.6% LBNK 0.430 +0.0% BARU 0.040 +0.0% VCU 1.08 −5.3% NOBL 0.100 +0.0% SHL 0.355 +0.0% MTS 0.130 +0.0% FYL 0.090 +0.0% NUAG 5.42 −0.6% CAM 0.330 −1.5% SYH 0.398 −1.9% LOT 0.040 +0.0% CPL 0.210 +10.5%
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Telo Genomics Presents Genomic Profiles of Peripheral Blood Minimal Residual Disease Cells at the 67th American Society of Hematology Meeting

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Executive Summary

  • Telo Genomics presented initial clinical data on a novel Minimal Residual Disease (MRD) test for Multiple Myeloma at the 67th ASH Annual Meeting.
  • The assay combines enumeration of circulating tumor cells (CTCs) from peripheral blood with 3‑D telomere profiling (TeloView®), achieving a limit of detection of 1 in 10⁷ cells.
  • Early results show distinct 3‑D genome profile clusters that correlate with high/low mutation rates, supporting potential prognostic use; larger validation studies are now underway.

Key Details

  • Presentation: Poster titled “Novel method of minimal residual disease testing in myeloma: liquid biopsies to enumerate and 3D telomere‑profile circulating tumor cells” presented by Dr. Yulia Shifrin (Laboratory Director).
  • Publication: Abstract published in the conference journal Blood; poster available on Telo Genomics website.
  • Assay Performance: Limit of detection = 1 myeloma cell per 10 million peripheral blood cells (1 × 10⁻⁷).
  • Technology: Integration of CTC enumeration with TeloView® 3‑D telomere profiling platform.
  • Biological Insight: Identified distinct clusters of 3‑D genome profiles that align with known high/low mutation rate patterns, offering functional information beyond simple cell counts.
  • Clinical Implication: Provides a less invasive alternative to bone‑marrow biopsies for continuous MRD monitoring; may aid in risk stratification and early detection of relapse.
  • Regulatory Context: FDA’s Oncologic Drugs Advisory Committee (April 2024) accepted MRD as an endpoint for accelerated approval of MM therapies, underscoring the relevance of MRD testing.
  • Market Outlook: Global MRD testing market projected to reach USD 4.1 billion by 2032; addressable market for MM assays estimated at >750,000 tests/year in the U.S.

Notable Quotes

“This method provides functional, biological information about the residual disease cells themselves, offering insights into progression risk beyond cell counts,” – Dr. Sabine Mai, Co‑founder and Interim CEO, Telo Genomics.


All boilerplate, forward‑looking disclaimer, and company background sections have been omitted for brevity.

Read the original news release →

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