Northwire Canada EditionTuesday, July 21, 2026
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LOD 0.280 −5.1% FVL 0.960 +5.5% BAG 0.210 +23.5% FMN 0.240 +0.0% OMM 0.050 +0.0% VUL 0.405 +0.0% PNTR 0.320 +8.5% SWA 0.035 +0.0% GEN 0.065 +0.0% PAT 0.355 +0.0% TOM 0.115 +9.5% ALS 57.10 +0.3% LIO 0.130 −7.1% GEMC 0.020 +0.0% CBA 0.070 +7.7% PUMA 0.110 +0.0% LOD 0.280 −5.1% FVL 0.960 +5.5% BAG 0.210 +23.5% FMN 0.240 +0.0% OMM 0.050 +0.0% VUL 0.405 +0.0% PNTR 0.320 +8.5% SWA 0.035 +0.0% GEN 0.065 +0.0% PAT 0.355 +0.0% TOM 0.115 +9.5% ALS 57.10 +0.3% LIO 0.130 −7.1% GEMC 0.020 +0.0% CBA 0.070 +7.7% PUMA 0.110 +0.0%
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Telo Genomics Highlights New MRD Methodology at The 2025 International Myeloma Society Meeting

TELO · Price

Executive Summary

  • Telo Genomics Corp. announced the presentation of a poster abstract on minimal residual disease (MRD) during the 22nd International Myeloma Society Annual Meeting in Toronto.
  • The presentation, led by Laboratory Director Dr. Yulia Shifrin, details a new workflow for MRD evaluation combining CTC enumeration with the TeloView® 3D telomere profiling platform.
  • The abstract will be published as a special supplement to the Clinical Lymphoma, Myeloma, & Leukemia Journal and made available on the Company website.

Key Details

  • Event: 22nd International Myeloma Society Annual Meeting (Toronto, Canada, September 17-20, 2025).
  • Presenter: Dr. Yulia Shifrin, Laboratory Director of Telo Genomics.
  • Abstract Title: "3D Telomere Profiling of MRD in Liquid Biopsy as a Predictive Marker of Disease Stability or Progression".
  • Technology Workflow: The presentation describes a workflow combining enumeration and immunophenotyping of individual Multiple Myeloma (MM) Circulating Tumor Cells (CTCs) with the TeloView® 3D telomere profiling platform.
  • Methodology Advantage: Evaluation of CTCs from peripheral blood (liquid biopsy) is highlighted as a less invasive biomarker allowing for continuous patient monitoring, offering functional and biologically actionable data on disease cells beyond simple enumeration.
  • Publication: Abstract to be published as a special supplement to the Clinical Lymphoma, Myeloma, & Leukemia Journal.
  • Market Context: The release notes the FDA's Oncologic Drugs Advisory Committee (ODAC) unanimous vote in April 2024 to accept MRD as a clinical endpoint for accelerated approval of new multiple myeloma therapies.
  • Market Size: The global MRD testing market is projected to reach USD 4.1 billion by 2032.
  • Target Market: The total addressable market for Multiple Myeloma (MM) assays is estimated at over 750,000 tests per year in the US.
  • Company Background: Telo Genomics has substantiated its proprietary technology in 160+ peer-reviewed publications and 30+ clinical studies involving more than 3,000 patients with multiple cancers and Alzheimer's disease. Its lead application, Telo-MM, is being developed for Multiple Myeloma.

Notable Quotes

  • No direct quotes from the CEO or President were included in the release text.
Read the original news release →

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