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Telo Genomics Corp. develops diagnostic and prognostic tests for human disease using 3D analysis of chromosomal telomeres. News about TDSGF centers on the company’s telomere analytics platform, including TeloView® and blood-based minimal residual disease testing for multiple myeloma.
Recurring updates include retrospective clinical studies and academic collaborations, presentations at hematology and myeloma meetings, laboratory-capacity developments, and corporate governance changes. Company announcements also describe work with circulating tumor cells, individual-cell risk profiling, and the use of liquid-biopsy workflows to assess relapse risk in oncology.
Telo Genomics Corp. (TSXV: TELO) (OTCQB: TDSGF) has received CLIA certification from the US Centers for Medicare & Medicaid Services. This important milestone allows Telo to offer its clinical laboratory services within the USA and develop and validate its TeloView prognostic products for distribution in the USA and other international jurisdictions recognizing International CLIA accreditation.
The CLIA certification, combined with the recently achieved CAP accreditation, enables Telo to demonstrate the viability of its TeloView prognostic products to potential US partners. This achievement is expected to advance Telo's platform of prognostic tests across oncology and empower ongoing partnership development efforts with key industry players, particularly in smoldering and minimal residual disease (MRD) in multiple myeloma.
Telo Genomics Corp. announced that its TeloViewSMM test for smoldering multiple myeloma (SMM) has been accepted as a Laboratory Developed Test (LDT) by the College of American Pathologists (CAP). This test, validated with Mayo Clinic and Dana Farber Cancer Institute, identifies high-risk SMM patients with 83% sensitivity and 76% specificity, helping to manage treatment intervention. The test will be added to Telo's CAP-approved menu, allowing it to be offered to US hospitals and cancer centers. CAP's approval was granted without an onsite assessment, reflecting Telo's prior demonstrated excellence.
Telo Genomics Corp. (TSXV: TELO, OTCQB: TDSGF, FSE: 3D0A) presented its AI-driven TeloView myeloma diagnostic tests at the ASCO 2024 meeting. The company introduced CellSelect-Pro™, a machine learning tool enhancing sample processing accuracy and efficiency, yielding a 20-25% cost saving over manual methods. CellSelect-Pro achieved over 90% accuracy and over 80% precision, validated with 20 patient samples. This tool integrates with Telo's TeloViewSMM for smoldering multiple myeloma (SMM) and is part of their MRD clinical trial at McGill University. Recently, Telo published a significant SMM study in the American Journal of Hematology, further validating their technology. President Sherif Louis highlighted the interest and positive reception of CellSelect-Pro at ASCO, marking a step toward commercialization and industry partnerships.
Telo Genomics announced the publication of results from its smoldering multiple myeloma (SMM) study in the American Journal of Hematology. The study, involving 168 patients, demonstrated superior performance of the TeloViewSMM test with an 85% positive predictive value and a 73% negative predictive value. The test, developed in collaboration with Mayo Clinic, distinguishes high-risk SMM patients from stable ones, aiding in treatment decisions. This non-invasive test addresses a critical need in SMM management and has potential applications in other cancers.
Telo Genomics (TSXV: TELO, OTCQB: TDSGF), a biotech firm specializing in telomere technology for oncology diagnostics, has entered into a collaboration with Emery Pharma, a CRO specializing in biologic drug development.
This partnership aims to merge their innovative technologies to provide enhanced bioanalytical solutions for clinical research. The TeloView platform from Telo offers high-sensitivity genomic instability insights, while Emery Pharma delivers comprehensive biologic characterization services.
The Memorandum of Understanding (MOU) sets the stage for collaborative efforts to address unmet needs in pharma and diagnostics. Executives from both companies expressed optimism about the potential synergies and future developments.
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