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Telo Genomics

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uuid00031z7

Namestring
Telo Genomics
Legal namestring
Telo Genomics Corp.
Websiteurl
telodx.com
Company typeenum
Public
Founded yearint
2015
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersToronto, Canada
HQ citystring
Toronto
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
molecular diagnostics, telomere profiling tests, multiple myeloma prognostics, minimal residual disease testing, liquid biopsy diagnostics
Industry4 codes
1Molecular Diagnostics & Genomics Laboratories
CodeHLAFAMAEPrimaryYes
2Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics)
CodeHLAAALADPrimaryNo
3Genomics & Molecular Diagnostics (Trial Support)
CodeHLAGAEADPrimaryNo
4Genetic, Cytogenetic & Prenatal Screening IVD
CodeHLAHAAAIPrimaryNo
NAICS code2 codes
  • Medical Laboratories621511
  • Medical and Diagnostic Laboratories6215
SIC code2 codes
  • Services-Medical Laboratories8071
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Molecular Diagnostics / Oncology and Neurology Prognostics
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Diagnostic Laboratory Testing Services
TypeProfessional Services
Description

Telo Genomics operates a CAP-accredited clinical laboratory offering proprietary diagnostic tests including TeloViewSMM. Physicians order tests through the SMART (physician experience) program, with tests processed in the company's Toronto laboratory.

telodx.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1TeloView®
Description

Proprietary 3D telomere analysis platform technology for diagnostics and prognostics in oncology and neurological diseases.

telodx.com
Core offering1 text field

Telo Genomics operates a CAP-accredited, CLIA-certified clinical laboratory offering proprietary molecular diagnostic tests built on its TeloView® 3D telomere profiling platform. Physicians and clinical partners order prognostic and diagnostic tests for Smoldering Multiple Myeloma (TeloViewSMM), Minimal Residual Disease in multiple myeloma (TeloMRD-D and TeloViewNG-MRD), first-line therapy management (TeloViewMM), Alzheimer's disease (TeloViewAD), and prostate cancer risk stratification (TeloViewPC), with tests processed in the company's Toronto laboratory and results returned to ordering physicians.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Sensitivity of 10-7 (detecting 1 cancer cell among 10 million cells) achieved in laboratory-prepared samples, exceeding current clinical sensitivity standards of 10-5 to 10-6
+2 more records
Product overview1 text field

Telo Genomics offers a platform-plus-products architecture centered on its proprietary TeloView® 3D telomere profiling technology. The core TeloView® platform analyzes six telomere parameters from single cells to provide prognostic and diagnostic insights across multiple disease areas. Commercial products include TeloViewSMM for smoldering multiple myeloma risk assessment, TeloMRD-D and TeloView®NG-MRD for minimal residual disease detection in multiple myeloma, TeloViewMM for first-line therapy management, TeloViewAD for Alzheimer's disease identification, and TeloViewPC for prostate cancer risk stratification. The company operates as a molecular diagnostics company with CAP-accredited and CLIA-certified laboratory facilities.

Product and service6 records
1TeloViewSMM
CategoryClinical Diagnostic Test - Multiple Myeloma Prognostics
Description

Laboratory Developed Test (LDT) prognostic solution for Smoldering Multiple Myeloma (SMM) that quantifies a patient's individual risk of progression from asymptomatic precursor SMM to symptomatic multiple myeloma within 2 years. Validated in collaboration with Mayo Clinic and Dana Farber Cancer Institute in over 170 SMM patients and published in the American Journal of Hematology. Intended for hematologists and oncologists managing SMM patients.

2TeloMRD-D
CategoryClinical Diagnostic Test - Minimal Residual Disease
Description

Enumeration-based Minimal Residual Disease (MRD) assay for multiple myeloma that directly counts circulating myeloma plasma cells isolated from peripheral blood using proprietary filtration, immunophenotyping, and fluorescence microscopy. Achieves sensitivity of up to 10^-7 (detecting 1 cancer cell among 10 million cells). Designed for hematologists and oncologists monitoring multiple myeloma patients for residual disease.

3TeloView®NG-MRD
CategoryClinical Diagnostic Test - Minimal Residual Disease
Description

Next-generation MRD assay that combines enumeration MRD with proprietary TeloView telomere profiling to assess the malignant potential (disease severity) of identified MRD cells. Goes beyond enumeration to profile the genomic instability of each identified circulating cell, differentiating aggressive clones prone to early relapse from benign clones indicating prolonged remission. Targets multiple myeloma MRD assessment.

4TeloViewMM
CategoryClinical Diagnostic Test - Multiple Myeloma Therapy Selection
Description

First-line therapy management test for multiple myeloma that predicts patient response to proposed first-line therapy and identifies relapse risk under standard treatment. Developed in clinical collaboration with Mayo Clinic with a risk scoring algorithm trained on an initial cohort. Designed to inform therapeutic decision-making for hematologists and oncologists, given treatment costs of $125,000-$250,000 per year.

5TeloViewAD
CategoryClinical Diagnostic Test - Neurology / Alzheimer's Disease
Description

Alzheimer's disease identification test designed to work from a non-invasive cheek swab sample. Uses TeloView parameters to identify Alzheimer's disease with high sensitivity and specificity from cheek cells. Predictive clinical algorithm being developed in collaboration with Sunnybrook Hospital. Aimed at neurologists and memory clinics seeking non-invasive tools to identify and stratify AD patients from mild to severe stages.

6TeloViewPC
CategoryClinical Diagnostic Test - Prostate Cancer Risk Stratification
Description

Prostate cancer biopsy-free risk prediction test that stratifies intermediate-risk (Gleason score 7) patients into aggressive versus benign disease categories to support biopsy and surgery decisions. Preliminary predictive risk algorithm is ready and the company is seeking clinical validation partners. Targeted at urologists managing intermediate-risk prostate cancer patients.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership11 partners
Strategic tierImportantTypeStrategic or Co-development PartnerAnnounced on2026-04-14
Description

Launched retrospective clinical study in April 2026 to validate blood-based assay for MRD testing in multiple myeloma patients. Study aims to demonstrate analytical sensitivity comparable to Euroflow and develop relapse risk scoring model.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-06-18
Description

Initiated new MRD clinical trial for multiple myeloma patients in June 2025. Cleveland Clinic Cancer Institute serves as clinical trial site for validating TeloMRD test.

Strategic tierImportantTypeImplementation/ SI/ Consulting PartnerAnnounced on2025-02-27
Description

Expanded partnership with Trusted Health Advisors in February 2025. Likely advisory support for US market development and physician engagement strategy.

Strategic tierImportantTypeTechnology or IntegrationAnnounced on2024-09-10
Description

Validated MRD enumeration assay with Adaptive Biotechnologies in September 2024. Evaluation focused on comparing TeloMRD-D enumeration capabilities with Adaptive's immune sequencing technology.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2024-05-15
Description

Collaboration announced May 2024. Details of collaboration scope not specified in available sources.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Major clinical validation partnership for Smoldering Multiple Myeloma test (TeloViewSMM) validated in over 170 patients. Expanded strategic collaboration in October 2024. Mayo Clinic handles clinical study execution with Telo providing technology platform.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Clinical validation collaboration for TeloViewSMM test in landmark publication in American Journal of Hematology. Dana Farber contributed clinical expertise and patient samples for validation study.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Telo Genomics founder Dr. Mai's research laboratory is located within CancerCare Manitoba/Research Institute in Oncology and Hematology. CCMB assigned all IP related to TeloView to Telo Genomics for commercialization. Continued research collaboration ongoing.

Strategic tierImportantTypeStrategic or Co-development Partner
Description

Collaboration for TeloViewAD Alzheimer's disease diagnostic development. Predictive clinical algorithm being developed for identifying Alzheimer's with high sensitivity and specificity from cheek cells.

Strategic tierCoreTypeTechnology or Integration
Description

CIMTEC, a renowned Canadian imaging-software developer, scaled and validated TeloView software. Critical technology partnership for commercializing the analytical software component.

11Sir Mortimer B. Davis - Jewish General Hospital
Strategic tierCoreTypeStrategic or Co-development Partner
Description

TELO-DMRD Clinical Trial (NCT05530096) collaboration with Dr. Rayan Kaedbey as Principal Investigator. Clinical validation site for MRD testing methodology.

telodx.com
Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Cancer genomics company offering tumor profiling and MRD (NeXT Personal). Comparable in stage and market to Telo, focused on tumor-informed MRD and minimal residual disease detection.

TypeOthers
Description

Life science tools and diagnostics company whose reagents and assay platforms are used in cancer research. While not a direct MRD competitor, Bio-Techne supplies enabling technologies to the molecular diagnostics ecosystem in which Telo operates.

TypeEmerging player
Description

Molecular profiling company offering comprehensive tumor profiling (MI Profile) and a developing MRD offering. Competes with Telo in advanced molecular characterization of cancer.

TypeDirect peer
Description

Provider of Signatera, a tumor-informed MRD test used across multiple oncology indications including multiple myeloma. Direct competitor in MRD monitoring with established US payer coverage and broad oncology channel access.

TypeBroad incumbent
Description

Established oncology-focused clinical laboratory offering comprehensive molecular and genetic testing including MRD via the RaDaR assay. Competes broadly with Telo in hematology/oncology reference testing.

TypeBroad incumbent
Description

Roche subsidiary offering comprehensive genomic profiling of solid tumors (FoundationOne CDx, FoundationOne Liquid CDx). Provides clinical decision support in oncology, partially overlapping with Telo's prognostic/monitoring positioning.

TypeDirect peer
Description

Developer of the FDA-approved clonoSEQ MRD test for multiple myeloma and other blood cancers. Direct MRD competitor to Telo's TeloMRD-D and TeloViewNG-MRD; the two companies also formally validated their respective MRD enumeration capabilities together in September 2024.

TypeBroad incumbent
Description

Established genetic testing company with oncology, women's health, and mental health franchises. Comparable to Telo as a multi-indication genetic/molecular diagnostics company, though at significantly larger scale.

TypeBroad incumbent
Description

Large molecular diagnostics company with Cologuard and a growing oncology franchise including the Oncodetect MRD test. A scaled competitor with deep commercial channels and FDA-cleared products.

TypeDirect peer
Description

Liquid biopsy company with MRD and oncology monitoring products (Guardant Reveal, Guardant360). Direct competitor in blood-based cancer monitoring, with significantly greater commercial scale and FDA-cleared assays.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability6 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Telo Genomics

Molecular Diagnostics / Oncology and Neurology Prognosticstelodx.com

Telo Genomics firmographics

Firmographics
Name
Telo Genomics
Legal name
Telo Genomics Corp.
Website
https://telodx.com
Company type
Public
Founded year
2015
Operating status
Operating
Headcount range
1–10 employees
Ownership category
akta.pro rank

Telo Genomics industry classification

Industry
Product category
Molecular Diagnostics / Oncology and Neurology Prognostics
NAICS
Medical Laboratories (621511), Medical and Diagnostic Laboratories (6215)
SIC
Services-Medical Laboratories (8071), In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Molecular Diagnostics & Genomics Laboratories (HLAFAMAE)
akta.pro secondary industries
Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics) (HLAAALAD), Genomics & Molecular Diagnostics (Trial Support) (HLAGAEAD), Genetic, Cytogenetic & Prenatal Screening IVD (HLAHAAAI)

Keywords

  • Molecular diagnostics
  • Telomere profiling tests
  • Multiple myeloma prognostics
  • Minimal residual disease testing
  • Liquid biopsy diagnostics

Where Telo Genomics is headquartered

Location

Headquarters

HQ city
Toronto
HQ country
Canada
HQ region
North America

Offices1 record

Markets served

Telo Genomics business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure

Revenue model

  1. Diagnostic Laboratory Testing Services: Telo Genomics operates a CAP-accredited clinical laboratory offering proprietary diagnostic tests including TeloViewSMM. Physicians order tests through the SMART (physician experience) program, with tests processed in the company's Toronto laboratory.

Go-to-market motion2 records

Distribution channels2 records

Marketing channels5 records

Telo Genomics product offering

Product offering

Core offering

Telo Genomics operates a CAP-accredited, CLIA-certified clinical laboratory offering proprietary molecular diagnostic tests built on its TeloView® 3D telomere profiling platform. Physicians and clinical partners order prognostic and diagnostic tests for Smoldering Multiple Myeloma (TeloViewSMM), Minimal Residual Disease in multiple myeloma (TeloMRD-D and TeloViewNG-MRD), first-line therapy management (TeloViewMM), Alzheimer's disease (TeloViewAD), and prostate cancer risk stratification (TeloViewPC), with tests processed in the company's Toronto laboratory and results returned to ordering physicians.

Product overview

Telo Genomics offers a platform-plus-products architecture centered on its proprietary TeloView® 3D telomere profiling technology. The core TeloView® platform analyzes six telomere parameters from single cells to provide prognostic and diagnostic insights across multiple disease areas. Commercial products include TeloViewSMM for smoldering multiple myeloma risk assessment, TeloMRD-D and TeloView®NG-MRD for minimal residual disease detection in multiple myeloma, TeloViewMM for first-line therapy management, TeloViewAD for Alzheimer's disease identification, and TeloViewPC for prostate cancer risk stratification. The company operates as a molecular diagnostics company with CAP-accredited and CLIA-certified laboratory facilities.

Differentiator

Problem solved

Functional benefit

Brands

  • TeloView®: Proprietary 3D telomere analysis platform technology for diagnostics and prognostics in oncology and neurological diseases.

Products and services

  • TeloViewSMM Laboratory Developed Test (LDT) prognostic solution for Smoldering Multiple Myeloma (SMM) that quantifies a patient's individual risk of progression from asymptomatic precursor SMM to symptomatic multiple myeloma within 2 years. Validated in collaboration with Mayo Clinic and Dana Farber Cancer Institute in over 170 SMM patients and published in the American Journal of Hematology. Intended for hematologists and oncologists managing SMM patients.
  • TeloMRD-D Enumeration-based Minimal Residual Disease (MRD) assay for multiple myeloma that directly counts circulating myeloma plasma cells isolated from peripheral blood using proprietary filtration, immunophenotyping, and fluorescence microscopy. Achieves sensitivity of up to 10^-7 (detecting 1 cancer cell among 10 million cells). Designed for hematologists and oncologists monitoring multiple myeloma patients for residual disease.
  • TeloView®NG-MRD Next-generation MRD assay that combines enumeration MRD with proprietary TeloView telomere profiling to assess the malignant potential (disease severity) of identified MRD cells. Goes beyond enumeration to profile the genomic instability of each identified circulating cell, differentiating aggressive clones prone to early relapse from benign clones indicating prolonged remission. Targets multiple myeloma MRD assessment.
  • TeloViewMM First-line therapy management test for multiple myeloma that predicts patient response to proposed first-line therapy and identifies relapse risk under standard treatment. Developed in clinical collaboration with Mayo Clinic with a risk scoring algorithm trained on an initial cohort. Designed to inform therapeutic decision-making for hematologists and oncologists, given treatment costs of $125,000-$250,000 per year.
  • TeloViewAD Alzheimer's disease identification test designed to work from a non-invasive cheek swab sample. Uses TeloView parameters to identify Alzheimer's disease with high sensitivity and specificity from cheek cells. Predictive clinical algorithm being developed in collaboration with Sunnybrook Hospital. Aimed at neurologists and memory clinics seeking non-invasive tools to identify and stratify AD patients from mild to severe stages.
  • TeloViewPC Prostate cancer biopsy-free risk prediction test that stratifies intermediate-risk (Gleason score 7) patients into aggressive versus benign disease categories to support biopsy and surgery decisions. Preliminary predictive risk algorithm is ready and the company is seeking clinical validation partners. Targeted at urologists managing intermediate-risk prostate cancer patients.

Quantifiable outcome

  • Sensitivity of 10-7 (detecting 1 cancer cell among 10 million cells) achieved in laboratory-prepared samples, exceeding current clinical sensitivity standards of 10-5 to 10-6
  • +2 more outcomes

Companies that use Telo Genomics

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles3 records

Telo Genomics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability6 records

Feature5 records

Telo Genomics partnerships and signals

Strategic signal

Partnerships

Eleven partnerships are on record, tiered important, core and minor.

  • National and Kapodistrian University of AthensimportantStrategic or Co-development Partner · 14 April 2026Launched retrospective clinical study in April 2026 to validate blood-based assay for MRD testing in multiple myeloma patients. Study aims to demonstrate analytical sensitivity comparable to Euroflow and develop relapse risk scoring model.
  • Cleveland CliniccoreStrategic or Co-development Partner · 18 June 2025Initiated new MRD clinical trial for multiple myeloma patients in June 2025. Cleveland Clinic Cancer Institute serves as clinical trial site for validating TeloMRD test.
  • Trusted Health AdvisorsimportantImplementation/ SI/ Consulting Partner · 27 February 2025Expanded partnership with Trusted Health Advisors in February 2025. Likely advisory support for US market development and physician engagement strategy.
  • Adaptive BiotechnologiesimportantTechnology or Integration · 10 September 2024Validated MRD enumeration assay with Adaptive Biotechnologies in September 2024. Evaluation focused on comparing TeloMRD-D enumeration capabilities with Adaptive's immune sequencing technology.
  • Emery PharmaminorStrategic or Co-development Partner · 15 May 2024Collaboration announced May 2024. Details of collaboration scope not specified in available sources.
  • Mayo CliniccoreStrategic or Co-development PartnerMajor clinical validation partnership for Smoldering Multiple Myeloma test (TeloViewSMM) validated in over 170 patients. Expanded strategic collaboration in October 2024. Mayo Clinic handles clinical study execution with Telo providing technology platform.
  • Dana Farber Cancer InstitutecoreStrategic or Co-development PartnerClinical validation collaboration for TeloViewSMM test in landmark publication in American Journal of Hematology. Dana Farber contributed clinical expertise and patient samples for validation study.
  • CancerCare ManitobacoreStrategic or Co-development PartnerTelo Genomics founder Dr. Mai's research laboratory is located within CancerCare Manitoba/Research Institute in Oncology and Hematology. CCMB assigned all IP related to TeloView to Telo Genomics for commercialization. Continued research collaboration ongoing.
  • Sunnybrook HospitalimportantStrategic or Co-development PartnerCollaboration for TeloViewAD Alzheimer's disease diagnostic development. Predictive clinical algorithm being developed for identifying Alzheimer's with high sensitivity and specificity from cheek cells.
  • Centre for Imaging Technology Commercialization (CIMTEC)coreTechnology or IntegrationCIMTEC, a renowned Canadian imaging-software developer, scaled and validated TeloView software. Critical technology partnership for commercializing the analytical software component.
  • Sir Mortimer B. Davis - Jewish General HospitalcoreStrategic or Co-development PartnerTELO-DMRD Clinical Trial (NCT05530096) collaboration with Dr. Rayan Kaedbey as Principal Investigator. Clinical validation site for MRD testing methodology.

Scale indicators9 records

Recent moves7 records

Expansion highlights6 records

Telo Genomics competitors and assessment

Company assessment

Emerging players

  • Personalis: Cancer genomics company offering tumor profiling and MRD (NeXT Personal). Comparable in stage and market to Telo, focused on tumor-informed MRD and minimal residual disease detection.
  • Caris Life Sciences: Molecular profiling company offering comprehensive tumor profiling (MI Profile) and a developing MRD offering. Competes with Telo in advanced molecular characterization of cancer.

Others

  • Bio-Techne: Life science tools and diagnostics company whose reagents and assay platforms are used in cancer research. While not a direct MRD competitor, Bio-Techne supplies enabling technologies to the molecular diagnostics ecosystem in which Telo operates.

Direct peers

  • Natera: Provider of Signatera, a tumor-informed MRD test used across multiple oncology indications including multiple myeloma. Direct competitor in MRD monitoring with established US payer coverage and broad oncology channel access.
  • Adaptive Biotechnologies: Developer of the FDA-approved clonoSEQ MRD test for multiple myeloma and other blood cancers. Direct MRD competitor to Telo's TeloMRD-D and TeloViewNG-MRD; the two companies also formally validated their respective MRD enumeration capabilities together in September 2024.
  • Guardant Health: Liquid biopsy company with MRD and oncology monitoring products (Guardant Reveal, Guardant360). Direct competitor in blood-based cancer monitoring, with significantly greater commercial scale and FDA-cleared assays.

Broad incumbents

  • NeoGenomics: Established oncology-focused clinical laboratory offering comprehensive molecular and genetic testing including MRD via the RaDaR assay. Competes broadly with Telo in hematology/oncology reference testing.
  • Foundation Medicine: Roche subsidiary offering comprehensive genomic profiling of solid tumors (FoundationOne CDx, FoundationOne Liquid CDx). Provides clinical decision support in oncology, partially overlapping with Telo's prognostic/monitoring positioning.
  • Myriad Genetics: Established genetic testing company with oncology, women's health, and mental health franchises. Comparable to Telo as a multi-indication genetic/molecular diagnostics company, though at significantly larger scale.
  • Exact Sciences: Large molecular diagnostics company with Cologuard and a growing oncology franchise including the Oncodetect MRD test. A scaled competitor with deep commercial channels and FDA-cleared products.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Telo Genomics social profiles

Digital presence

Telo Genomics compliance and trust

Trust signal

Compliance3 records

Telo Genomics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Telo Genomics leadership team

Management profile

Number of profiles

Profiles7 records

Telo Genomics funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Telo Genomics M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Telo Genomics

What does Telo Genomics do?

Telo Genomics operates a CAP-accredited, CLIA-certified clinical laboratory offering proprietary molecular diagnostic tests built on its TeloView® 3D telomere profiling platform. Physicians and clinical partners order prognostic and diagnostic tests for Smoldering Multiple Myeloma (TeloViewSMM), Minimal Residual Disease in multiple myeloma (TeloMRD-D and TeloViewNG-MRD), first-line therapy management (TeloViewMM), Alzheimer's disease (TeloViewAD), and prostate cancer risk stratification (TeloViewPC), with tests processed in the company's Toronto laboratory and results returned to ordering physicians.

Is Telo Genomics a public or private company?

Telo Genomics is a public company. It is classified as public and is currently operating.

When was Telo Genomics founded?

Telo Genomics was founded in 2015. It employs 1 to 10 people.

Where is Telo Genomics based?

Telo Genomics is headquartered in Toronto, Canada, in the North America region.

How does Telo Genomics make money?

One revenue line is on record: diagnostic Laboratory Testing Services.

Who are Telo Genomics's main competitors?

Emerging players on record are Personalis and Caris Life Sciences. Bio-Techne is listed as an others. Direct peers are Natera, Adaptive Biotechnologies and Guardant Health. Broad incumbents are NeoGenomics, Foundation Medicine, Myriad Genetics and Exact Sciences.

Does Telo Genomics have an API?

No public API is recorded for Telo Genomics.

What industry is Telo Genomics in?

Telo Genomics's product category is Molecular Diagnostics / Oncology and Neurology Prognostics. Its primary akta.pro industry code is HLAFAMAE, Molecular Diagnostics & Genomics Laboratories, with a secondary code of HLAAALAD, Genetic & Genomic Testing (germline, somatic, carrier, pharmacogenomics). Its NAICS code is 621511 and its SIC code is 8071.

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Live signals
AktienTelo Genomics Reports Additional Clinical Research Results Comparing Blood-Based TELO-MRD with Bone-Marrow Next-Generation Flow and Next-Generation SequencingTelo Genomics reported additional clinical research results comparing its blood-based TELO-MRD assay with bone marrow Adaptive clonoSEQ NGS testing in matched samples from Cleveland Clinic and Jewish General Hospital. The blood-based test detected circulating plasma cells in all Adaptive clonoSEQ-positive cases and some negative samples, and the company summarized previously reported EuroFlow comparison data.BioSpaceTelo Genomics Announces Clinical Research Results Evidencing Utility of Its Telomere Analysis Platform in Predicting Multiple Myeloma RelapseTelo Genomics reported clinical results showing its TELO-MRD blood-based assay detected residual myeloma cells in 92.9% of matched samples versus 54.8% by bone-marrow EuroFlow NGF. The company also introduced a TELO-MRD scoring model to estimate relapse risk, with commercialization targeted by end of 2027.NewsfileTelo Genomics Grants Stock OptionsTelo Genomics Corp. announced the grant of stock options to purchase up to 3,300,000 common shares, with 2,500,000 allocated to directors and officers, 600,000 to employees, and 200,000 to consultants. The options have an exercise price of $0.055 per share, vest immediately, and expire five years from the grant date, subject to TSX Venture Exchange approval and a four-month hold period. The company stated the grants were made to reward and incentivize team contributions to the company's success.YahooTelo Genomics Grants Stock OptionsTelo Genomics Corp. announced the grant of stock options to purchase up to 3,300,000 common shares to its directors, officers, employees, and consultants, subject to TSX Venture Exchange approval. Of the total options, 2,500,000 were allocated to directors and officers, 600,000 to employees, and 200,000 to consultants, exercisable at $0.055 per share with immediate vesting and a five-year expiration. The company stated the grants are intended to reward and incentivize the team for their past and ongoing contributions to Telo Genomics' success.Stock TitanTelo Genomics' 3.3M Options Await TSXV ApprovalTelo Genomics Corp. announced the grant of stock options to purchase up to 3,300,000 common shares at $0.055 per share, subject to TSX Venture Exchange approval. Of the total, 2,500,000 options were granted to directors and officers, 600,000 to employees, and 200,000 to consultants, with all options vesting immediately and expiring five years from the grant date. The company stated the options are intended to reward the team for past and ongoing efforts and incentivize future contributions to Telo Genomics' success.NewsfileTelo Genomics Provides Positive Interim Data from Ongoing Clinical Trial Advancing Genomic Instability-Based Relapse Risk AssessmentTelo Genomics Corp. announced positive interim results from an ongoing retrospective clinical study conducted with the National and Kapodistrian University of Athens, analyzing baseline blood samples from 50 multiple myeloma patients treated with standard-of-care regimens. The study identified a telomere-associated nuclear architecture parameter as the strongest predictor of relapse status, achieving an Area Under the Curve (AUC) of 0.849, which is considered highly predictive in clinical diagnostics. The company believes its platform may complement existing MRD technologies and potentially reduce reliance on invasive bone marrow biopsies for relapse-risk assessment in multiple myeloma and other cancers.Stock TitanTelo Genomics Shows 0.849 AUC in Myeloma StudyTelo Genomics Corp. announced positive interim results from an ongoing retrospective clinical study showing its blood-based assay achieved an AUC of 0.849 in predicting relapse risk for multiple myeloma patients. The study, conducted in collaboration with National and Kapodistrian University of Athens, identified telomere-associated nuclear architecture parameters as the strongest predictor of relapse status. The company has also partnered with Cleveland Clinic and Montreal Jewish General Hospital for additional validation studies, with the primary trial expected to conclude in summer 2026.BioSpaceTelo Genomics Provides Positive Interim Data from Ongoing Clinical Trial Advancing Genomic Instability-Based Relapse Risk AssessmentTelo Genomics announced positive interim results from a clinical trial analyzing blood samples from 50 multiple myeloma patients. The assay achieved an AUC of 0.849, predicting relapse risk via telomere architecture. The trial is expected to conclude in summer 2026.NewsfileTelo Genomics Files Patent to Expand IP Portfolio to Liquid Biopsy MRD Applications for Multiple MyelomaTelo Genomics Corp. filed a U.S. provisional patent application to protect a new TeloView® biomarker algorithm for use with liquid biopsy samples in managing minimal residual disease (MRD) for multiple myeloma patients. The algorithm can predict relapse risk and isolate circulating cancer cells from peripheral blood, offering a non-invasive alternative to current bone marrow-based MRD testing methods. The company, in collaboration with the University of Athens, is validating the clinical assay which it expects to lower healthcare costs and improve patient outcomes.Stock TitanTelo Genomics files U.S. patent for myeloma MRDTelo Genomics Corp. has filed a U.S. provisional patent application to protect a new TeloView® biomarker algorithm designed for liquid biopsy applications in detecting minimal residual disease (MRD) in multiple myeloma patients. The algorithm predicts relapse risk and isolates circulating cancer cells from peripheral blood samples, offering a non-invasive alternative to current bone marrow sampling methods that require invasive procedures. The company, collaborating with the University of Athens on ongoing validation studies, expects this blood-based MRD assay to lower healthcare costs and improve patient care outcomes while strengthening its competitive position in the MRD diagnostics space.