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CNSide Diagnostics

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uuid00sxwp9

Namestring
CNSide Diagnostics
Legal namestring
CNSide Diagnostics, LLC
Websiteurl
cnside-dx.com
Company typeenum
Private
Founded yearint
2024
Descriptiontext

CNSide Diagnostics is a Houston-based molecular diagnostics company operating as a wholly-owned subsidiary of Plus Therapeutics (NASDAQ:PSTV). The company develops and commercializes the CNSide CSF Assay Platform, a proprietary cerebrospinal fluid assay designed to detect, quantify, and molecularly characterize tumor cells in CSF. Its primary clinical application is the diagnosis and monitoring of leptomeningeal metastases, a serious oncology complication involving spread of disease to the membranes surrounding the brain and spinal cord. The customer base comprises neuro-oncologists, oncologists, NCI-designated cancer centers, and academic medical centers, totaling more than 120 institutional accounts.

The platform combines a proprietary multi-antibody microfluidic cell-capture architecture with the CEE-Sure collection and shipping tube, enabling external sites to ship CSF specimens to CNSide's CLIA-accredited, CAP-accredited Houston laboratory for centralized analysis. CNSide has vertically integrated in-house manufacturing of its collection tubes, antibody mixes, and microfluidic chips, which reduces supply risk and tightens control over pre-analytic quality. The business model is fee-for-service clinical laboratory testing, with billing routed through commercial payers, Medicare, and the dedicated CPT code 0640U.

Following a $15M public offering in January 2026, the achievement of CLIA, CAP, and Medicare regulatory milestones, and a national coverage agreement with Elevance Health, CNSide has expanded operations to roughly 48-50 states with payer reach extending to approximately 126 million covered lives. The company is preparing to broaden its menu with CSF-based ICC, FISH, and NGS assays in 2026 and has signaled intent to expand internationally after U.S. scale is established.

Short descriptiontext

CNSide Diagnostics, a Houston-based subsidiary of Plus Therapeutics, operates a CLIA-accredited molecular diagnostics laboratory running the proprietary CNSide CSF Assay Platform to detect and characterize tumor cells in cerebrospinal fluid for neuro-oncologists managing leptomeningeal metastases.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersHouston, United States
HQ citystring
Houston
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
liquid biopsy diagnostics, cerebrospinal fluid testing, leptomeningeal metastases detection, molecular cancer diagnostics, tumor cell enumeration
Industry3 codes
1Oncology Diagnostics (tumor profiling, MRD, liquid biopsy)
CodeHLAAALAEPrimaryYes
2Cytology & Histopathology Diagnostics (IHC, ISH, tissue-based assays)
CodeHLAAALAIPrimaryNo
3Specialty & Biomarker Laboratory Services (Immunoassays/Flow/Cytometry)
CodeHLAGAEABPrimaryNo
NAICS code3 codes
  • Medical Laboratories621511
  • In-Vitro Diagnostic Substance Manufacturing325413
  • Medical and Diagnostic Laboratories62151
SIC code2 codes
  • Services-Medical Laboratories8071
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Molecular Diagnostics
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Laboratory Testing Services
TypeOne Time License
Description

CNSide Diagnostics generates revenue through clinical laboratory testing services. The company bills commercial payers, Medicare, and patients for its CSF tumor cell enumeration test. A new CPT code (0640U) became effective July 1, 2026, enabling standardized billing and claims processing.

in.investing.com
2Commercial Payer Agreements
TypeSubscription Recurring
Description

Revenue generated through coverage agreements with commercial health insurers including United Healthcare, Humana, Highmark, Blue Shield of California, and Elevance Health. The company has approximately 126 million total contracted covered lives as of June 2026.

in.investing.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
Pricing details1 tier
1Insurance-based billing through commercial payers and Medicare
ModelTransaction based/ take rateBilling cadencePay-as-you-go
Notes

Billed through CPT code 0640U effective July 1, 2026. Coverage varies by health plan and clinical circumstances. Interest-free payment plans available for patient responsibility under $500 (up to 6 months) or over $500 (up to 12 months).

in.investing.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1CNSide® CSF Assay Platform
Description

A proprietary cerebrospinal fluid assay platform that provides tumor cell enumeration and molecular characterization for managing leptomeningeal metastases and CNS cancers.

cnside-dx.com
+1 more record
Core offering1 text field

CNSide Diagnostics operates a CLIA-certified clinical laboratory that runs the proprietary CNSide® CSF Assay Platform, with the commercially available CNSide® CSF Tumor Cell Enumeration (TCE) test detecting and quantifying tumor cells in cerebrospinal fluid for diagnosing and monitoring leptomeningeal metastases. The company also manufactures the proprietary CEE-Sure® CSF Collection Tube preservative used to stabilize CSF specimens during transport, and is developing molecular characterization tests (ICC, FISH, NGS) on the same CSF sample.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 92% sensitivity and 95% specificity for leptomeningeal metastases detection
+3 more records
Product overview1 text field

CNSide Diagnostics offers the CNSide® Cerebrospinal Fluid (CSF) Assay Platform, a suite of molecular diagnostic tests for detecting and analyzing cancer cells in cerebrospinal fluid. The platform currently includes the commercially available CNSide® CSF Tumor Cell Enumeration (TCE) test, with additional tests in development including CSF ICC, FISH, and NGS tests expected to launch in 2026. The company manufactures key test components including the CEE-Sure® CSF collection tube preservative, antibody mix, and microfluidic chip in-house at its Houston, Texas facility for vertical integration and scalability. The platform enables rapid diagnosis, treatment monitoring, and treatment guidance for patients with leptomeningeal metastases.

Product and service2 records
1CNSide CSF Tumor Cell Enumeration (TCE) Test
CategoryMolecular Diagnostics / Liquid Biopsy
Description

Clinical laboratory test that detects, quantifies, and reports tumor cells in cerebrospinal fluid using the proprietary CNSide CSF Assay Platform; intended for neuro-oncologists and oncologists diagnosing and monitoring leptomeningeal metastases from solid tumors.

2CEE-Sure CSF Collection Tube
CategorySpecimen Collection / Pre-analytical Consumable
Description

Proprietary specimen collection tube containing a preservative that stabilizes cerebrospinal fluid during transport to the CNSide Diagnostics CLIA laboratory, supporting the integrity of the Tumor Cell Enumeration test.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeOthers
Description

CNSide Diagnostics, LLC is a wholly-owned subsidiary of Plus Therapeutics, Inc. (NASDAQ: PSTV). Plus Therapeutics acquired all CNSide® assets and established CNSide Diagnostics in 2024. The subsidiary operates independently to commercialize the CNSide CSF Assay Platform while Plus Therapeutics focuses on its radiopharmaceutical pipeline including REYOBIQ.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Leading oncology liquid biopsy company with Guardant360 CDx and Guardant Reveal MRD products using cell-free DNA approaches. Most directly comparable peer in the blood-based oncology liquid biopsy category, sharing CNSide's strategy of using rare-cell/DNA analytics to guide solid tumor treatment.

TypeDirect peer
Description

Molecular diagnostics company offering NeXT Personal (tumor-informed MRD) for solid tumors. Direct peer in liquid biopsy MRD and treatment monitoring for oncology, with similar payer coverage focus.

TypeDirect peer
Description

Originally developed and commercialized the CNSide® CSF assay platform beginning in 2020; CNSide Diagnostics was established in 2024 when Plus Therapeutics acquired all CNSide assets from the prior program. Biocept represents the most direct historical predecessor in CSF-based liquid biopsy for oncology.

TypeDirect peer
Description

Oncology liquid biopsy peer commercializing Signatera for molecular residual disease (MRD) monitoring and treatment response assessment. Shares CNSide's molecular treatment-monitoring positioning and similar payer-coverage expansion strategy across U.S. oncology.

TypeDirect peer
Description

AI-powered precision medicine company offering xT (tissue), xR (liquid biopsy/RNA), and xF (ctDNA) oncology diagnostics. Comparable peer combining molecular profiling with proprietary data/molecular tumor board workflows for academic oncology centers.

TypeDirect peer
Description

Subsidiary of Roche providing comprehensive genomic profiling (FoundationOne CDx) and liquid biopsy (FoundationOne Liquid CDx) for solid tumors. A direct molecular tumor profiling and liquid biopsy peer with overlapping clinical customers (academic medical centers, oncologists).

TypeBroad incumbent
Description

Larger oncology diagnostics incumbent with Cologuard (screening) and Oncotype DX (tumor profiling), now expanding into MRD via the Thrive acquisition. Comparable on payer contracting scale and commercial U.S. footprint but broader, more diversified than CNSide's leptomeningeal focus.

TypeEmerging player
Description

China-based oncology liquid biopsy company commercializing tumor profiling and MRD assays. Comparable technology and clinical positioning with CNSide, but operating from a different geography and primarily serving the Chinese market.

TypeDirect peer
Description

Molecular profiling company offering MI Profile (tissue) and MI Cancer Seek (blood) for solid tumor molecular characterization and MRD. Directly comparable on molecular tumor profiling and CNS-adjacent cancer applications.

TypeDirect peer
Description

Oncology-focused clinical laboratory and molecular diagnostics company offering comprehensive tumor profiling, including liquid biopsy services. Closely comparable specialty lab operating model with similar payer coverage and academic cancer center customer focus.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 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 profile1 record

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 maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 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 rounds

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 →

CNSide Diagnostics

Molecular Diagnosticscnside-dx.com

CNSide Diagnostics, a Houston-based subsidiary of Plus Therapeutics, operates a CLIA-accredited molecular diagnostics laboratory running the proprietary CNSide CSF Assay Platform to detect and characterize tumor cells in cerebrospinal fluid for neuro-oncologists managing leptomeningeal metastases.

What CNSide Diagnostics does

CNSide Diagnostics is a Houston-based molecular diagnostics company operating as a wholly-owned subsidiary of Plus Therapeutics (NASDAQ:PSTV). The company develops and commercializes the CNSide CSF Assay Platform, a proprietary cerebrospinal fluid assay designed to detect, quantify, and molecularly characterize tumor cells in CSF. Its primary clinical application is the diagnosis and monitoring of leptomeningeal metastases, a serious oncology complication involving spread of disease to the membranes surrounding the brain and spinal cord. The customer base comprises neuro-oncologists, oncologists, NCI-designated cancer centers, and academic medical centers, totaling more than 120 institutional accounts.

The platform combines a proprietary multi-antibody microfluidic cell-capture architecture with the CEE-Sure collection and shipping tube, enabling external sites to ship CSF specimens to CNSide's CLIA-accredited, CAP-accredited Houston laboratory for centralized analysis. CNSide has vertically integrated in-house manufacturing of its collection tubes, antibody mixes, and microfluidic chips, which reduces supply risk and tightens control over pre-analytic quality. The business model is fee-for-service clinical laboratory testing, with billing routed through commercial payers, Medicare, and the dedicated CPT code 0640U.

Following a $15M public offering in January 2026, the achievement of CLIA, CAP, and Medicare regulatory milestones, and a national coverage agreement with Elevance Health, CNSide has expanded operations to roughly 48-50 states with payer reach extending to approximately 126 million covered lives. The company is preparing to broaden its menu with CSF-based ICC, FISH, and NGS assays in 2026 and has signaled intent to expand internationally after U.S. scale is established.

CNSide Diagnostics firmographics

Firmographics
Name
CNSide Diagnostics
Legal name
CNSide Diagnostics, LLC
Website
https://cnside-dx.com
Company type
Private
Founded year
2024
Operating status
Operating
Headcount range
11–50 employees
Short description
CNSide Diagnostics, a Houston-based subsidiary of Plus Therapeutics, operates a CLIA-accredited molecular diagnostics laboratory running the proprietary CNSide CSF Assay Platform to detect and characterize tumor cells in cerebrospinal fluid for neuro-oncologists managing leptomeningeal metastases.
Ownership category
akta.pro rank

CNSide Diagnostics industry classification

Industry
Product category
Molecular Diagnostics
NAICS
Medical Laboratories (621511), In-Vitro Diagnostic Substance Manufacturing (325413), Medical and Diagnostic Laboratories (62151)
SIC
Services-Medical Laboratories (8071), In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Oncology Diagnostics (tumor profiling, MRD, liquid biopsy) (HLAAALAE)
akta.pro secondary industries
Cytology & Histopathology Diagnostics (IHC, ISH, tissue-based assays) (HLAAALAI), Specialty & Biomarker Laboratory Services (Immunoassays/Flow/Cytometry) (HLAGAEAB)

Keywords

  • Liquid biopsy diagnostics
  • Cerebrospinal fluid testing
  • Leptomeningeal metastases detection
  • Molecular cancer diagnostics
  • Tumor cell enumeration

Where CNSide Diagnostics is headquartered

Location

Headquarters

HQ city
Houston
HQ country
United States
HQ region
North America

Offices1 record

Markets served

CNSide Diagnostics business model

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

Revenue model

  1. Laboratory Testing Services: CNSide Diagnostics generates revenue through clinical laboratory testing services. The company bills commercial payers, Medicare, and patients for its CSF tumor cell enumeration test. A new CPT code (0640U) became effective July 1, 2026, enabling standardized billing and claims processing.
  2. Commercial Payer Agreements: Revenue generated through coverage agreements with commercial health insurers including United Healthcare, Humana, Highmark, Blue Shield of California, and Elevance Health. The company has approximately 126 million total contracted covered lives as of June 2026.

Pricing tiers

ModelBillingPrice
Transaction based/ take ratePay-as-you-goInsurance-based billing through commercial payers and Medicare

Go-to-market motion2 records

Distribution channels1 record

Marketing channels6 records

CNSide Diagnostics product offering

Product offering

Core offering

CNSide Diagnostics operates a CLIA-certified clinical laboratory that runs the proprietary CNSide® CSF Assay Platform, with the commercially available CNSide® CSF Tumor Cell Enumeration (TCE) test detecting and quantifying tumor cells in cerebrospinal fluid for diagnosing and monitoring leptomeningeal metastases. The company also manufactures the proprietary CEE-Sure® CSF Collection Tube preservative used to stabilize CSF specimens during transport, and is developing molecular characterization tests (ICC, FISH, NGS) on the same CSF sample.

Product overview

CNSide Diagnostics offers the CNSide® Cerebrospinal Fluid (CSF) Assay Platform, a suite of molecular diagnostic tests for detecting and analyzing cancer cells in cerebrospinal fluid. The platform currently includes the commercially available CNSide® CSF Tumor Cell Enumeration (TCE) test, with additional tests in development including CSF ICC, FISH, and NGS tests expected to launch in 2026. The company manufactures key test components including the CEE-Sure® CSF collection tube preservative, antibody mix, and microfluidic chip in-house at its Houston, Texas facility for vertical integration and scalability. The platform enables rapid diagnosis, treatment monitoring, and treatment guidance for patients with leptomeningeal metastases.

Differentiator

Problem solved

Functional benefit

Brands

  • CNSide® CSF Assay Platform: A proprietary cerebrospinal fluid assay platform that provides tumor cell enumeration and molecular characterization for managing leptomeningeal metastases and CNS cancers.
  • CNSide® CSF Tumor Cell Enumeration (TCE)

Products and services

  • CNSide CSF Tumor Cell Enumeration (TCE) Test Clinical laboratory test that detects, quantifies, and reports tumor cells in cerebrospinal fluid using the proprietary CNSide CSF Assay Platform; intended for neuro-oncologists and oncologists diagnosing and monitoring leptomeningeal metastases from solid tumors.
  • CEE-Sure CSF Collection Tube Proprietary specimen collection tube containing a preservative that stabilizes cerebrospinal fluid during transport to the CNSide Diagnostics CLIA laboratory, supporting the integrity of the Tumor Cell Enumeration test.

Quantifiable outcome

  • 92% sensitivity and 95% specificity for leptomeningeal metastases detection
  • +3 more outcomes

Companies that use CNSide Diagnostics

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles1 record

CNSide Diagnostics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

CNSide Diagnostics partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Plus Therapeutics, Inc.coreOthersCNSide Diagnostics, LLC is a wholly-owned subsidiary of Plus Therapeutics, Inc. (NASDAQ: PSTV). Plus Therapeutics acquired all CNSide® assets and established CNSide Diagnostics in 2024. The subsidiary operates independently to commercialize the CNSide CSF Assay Platform while Plus Therapeutics focuses on its radiopharmaceutical pipeline including REYOBIQ.

Scale indicators7 records

Recent moves8 records

Expansion highlights6 records

CNSide Diagnostics competitors and assessment

Company assessment

Direct peers

  • Guardant Health: Leading oncology liquid biopsy company with Guardant360 CDx and Guardant Reveal MRD products using cell-free DNA approaches. Most directly comparable peer in the blood-based oncology liquid biopsy category, sharing CNSide's strategy of using rare-cell/DNA analytics to guide solid tumor treatment.
  • Personalis: Molecular diagnostics company offering NeXT Personal (tumor-informed MRD) for solid tumors. Direct peer in liquid biopsy MRD and treatment monitoring for oncology, with similar payer coverage focus.
  • Biocept: Originally developed and commercialized the CNSide® CSF assay platform beginning in 2020; CNSide Diagnostics was established in 2024 when Plus Therapeutics acquired all CNSide assets from the prior program. Biocept represents the most direct historical predecessor in CSF-based liquid biopsy for oncology.
  • Natera: Oncology liquid biopsy peer commercializing Signatera for molecular residual disease (MRD) monitoring and treatment response assessment. Shares CNSide's molecular treatment-monitoring positioning and similar payer-coverage expansion strategy across U.S. oncology.
  • Tempus AI: AI-powered precision medicine company offering xT (tissue), xR (liquid biopsy/RNA), and xF (ctDNA) oncology diagnostics. Comparable peer combining molecular profiling with proprietary data/molecular tumor board workflows for academic oncology centers.
  • Foundation Medicine: Subsidiary of Roche providing comprehensive genomic profiling (FoundationOne CDx) and liquid biopsy (FoundationOne Liquid CDx) for solid tumors. A direct molecular tumor profiling and liquid biopsy peer with overlapping clinical customers (academic medical centers, oncologists).
  • Caris Life Sciences: Molecular profiling company offering MI Profile (tissue) and MI Cancer Seek (blood) for solid tumor molecular characterization and MRD. Directly comparable on molecular tumor profiling and CNS-adjacent cancer applications.
  • NeoGenomics: Oncology-focused clinical laboratory and molecular diagnostics company offering comprehensive tumor profiling, including liquid biopsy services. Closely comparable specialty lab operating model with similar payer coverage and academic cancer center customer focus.

Broad incumbents

  • Exact Sciences: Larger oncology diagnostics incumbent with Cologuard (screening) and Oncotype DX (tumor profiling), now expanding into MRD via the Thrive acquisition. Comparable on payer contracting scale and commercial U.S. footprint but broader, more diversified than CNSide's leptomeningeal focus.

Emerging players

  • Burning Rock Biotech: China-based oncology liquid biopsy company commercializing tumor profiling and MRD assays. Comparable technology and clinical positioning with CNSide, but operating from a different geography and primarily serving the Chinese market.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks7 records

Key highlights7 records

Customer concentration

CNSide Diagnostics social profiles

Digital presence

CNSide Diagnostics compliance and trust

Trust signal

Compliance3 records

CNSide Diagnostics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CNSide Diagnostics leadership team

Management profile

Number of profiles

Profiles10 records

CNSide Diagnostics funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

CNSide Diagnostics 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 CNSide Diagnostics

What does CNSide Diagnostics do?

CNSide Diagnostics operates a CLIA-certified clinical laboratory that runs the proprietary CNSide® CSF Assay Platform, with the commercially available CNSide® CSF Tumor Cell Enumeration (TCE) test detecting and quantifying tumor cells in cerebrospinal fluid for diagnosing and monitoring leptomeningeal metastases. The company also manufactures the proprietary CEE-Sure® CSF Collection Tube preservative used to stabilize CSF specimens during transport, and is developing molecular characterization tests (ICC, FISH, NGS) on the same CSF sample.

Is CNSide Diagnostics a public or private company?

CNSide Diagnostics is a private company. It is classified as corporate owned and is currently operating.

When was CNSide Diagnostics founded?

CNSide Diagnostics was founded in 2024. It employs 11 to 50 people.

Where is CNSide Diagnostics based?

CNSide Diagnostics is headquartered in Houston, United States, in the North America region.

How does CNSide Diagnostics make money?

Two revenue lines are on record. Laboratory Testing Services are the primary driver. The others are commercial Payer Agreements.

Who are CNSide Diagnostics's main competitors?

Direct peers on record are Guardant Health, Personalis, Biocept, Natera, Tempus AI, Foundation Medicine, Caris Life Sciences and NeoGenomics. Exact Sciences is listed as a broad incumbent. Burning Rock Biotech is listed as an emerging player.

Does CNSide Diagnostics have an API?

No public API is recorded for CNSide Diagnostics.

What industry is CNSide Diagnostics in?

CNSide Diagnostics's product category is Molecular Diagnostics. Its primary akta.pro industry code is HLAAALAE, Oncology Diagnostics (tumor profiling, MRD, liquid biopsy), with a secondary code of HLAAALAI, Cytology & Histopathology Diagnostics (IHC, ISH, tissue-based assays). Its NAICS code is 621511 and its SIC code is 8071.

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Live signals
Quiver QuantitativeCerenome Subsidiary CNSide Diagnostics Launches CSF Molecular Profiling Tests for CNS Cancers | CNSY Stock NewsCNSide Diagnostics, a Cerenome subsidiary, launched two CSF molecular profiling tests for CNS tumors and hematologic malignancies on October 12, 2026. The tests analyze over 300 cancer-related genes and 1,600 RNA transcripts, with a study showing cancer-related findings in 78.4% of specimens. The tests are laboratory developed and not FDA cleared.BioSpaceCerenome Expects $1.55 Million in CNSide® Third Quarter Gross BillingsCerenome reported Q3 2026 CNSide gross billings of $1.55 million from 222 tests, with initial collections expected in Q4. The company expects to reach 200 million covered lives by early 2027 and launch expanded testing in Q4 2026.Quiver QuantitativeCerenome to Host September 30 Conference Call on CNSide Diagnostics Business Update | CNSY Stock NewsCNSide Diagnostics, a Cerenome subsidiary, will host a conference call on September 30, 2026, to update stakeholders on its CNSide cerebrospinal fluid diagnostic platform. The call will cover third-party billing, market access, commercial team expansion, and portfolio broadening. The company aims to grow its business by 2026.The future of tradingCerenome unit CNSide Diagnostics sets Sept. 30 CNSide business update callCNSide Diagnostics, a Cerenome unit, will host a business update call on Sept. 30, 2026. The call centers on commercial execution for the CNSide cerebrospinal fluid diagnostic platform launched in early 2026, addressing third-party billing, market access, commercial team expansion, and portfolio broadening.Quiver QuantitativeCerenome’s CNSide Diagnostics Secures In-Network Agreement with Blue Cross Blue Shield of Michigan for CNSide CSF Tumor Cell Assay | CNSY Stock NewsCNSide Diagnostics signed an in-network agreement with Blue Cross Blue Shield of Michigan to offer its CNSide CSF Tumor Cell Enumeration assay, effective September 1, 2026. The agreement covers about 5 million members, bringing total contracted coverage to approximately 158 million lives. The company aims to expand U.S. reimbursement coverage to improve patient access.citybizCerenome Names Samantha Fowlkes to Lead CNSide Commercial SalesCerenome appointed Samantha Fowlkes as vice president and head of commercial sales for its CNSide Diagnostics division. She will oversee expansion of the cerebrospinal fluid-based testing platform for CNS cancers, building a sales organization. The role supports Cerenome's integrated CNS oncology model, including its REYOBIQ therapeutic platform.Quiver QuantitativeCerenome Appoints Samantha Fowlkes as Vice President, Head of Commercial Sales for CNSide Diagnostics | CNSY Stock NewsCNSide Diagnostics, a Cerenome subsidiary, appointed Samantha Fowlkes as Vice President Head of Commercial Sales to drive commercial growth of its CNSide platform in oncology and pathology. Fowlkes brings over 20 years of experience in oncology diagnostics and precision medicine, having previously led at Caris Life Sciences and Genoptix. The appointment aims to expand adoption of CNSide's cerebrospinal fluid-based testing for CNS cancers.BioSpaceCerenome Appoints Samantha Fowlkes as Vice President and Head of Commercial Sales, CNSide Diagnostics DivisionCerenome appointed Samantha Fowlkes as Vice President Head of Commercial Sales for its CNSide Diagnostics subsidiary. She will lead commercial expansion of CNSide, building relationships across oncology and pathology communities. The role aims to accelerate adoption of the CNSide platform by physicians and health systems.Investing.comCNSide Diagnostics signs coverage deal with HCSC for CSF assay By Investing.comCNSide Diagnostics, a subsidiary of Cerenome Inc., signed an in-network provider agreement with Health Care Service Corporation (HCSC) effective August 1 to cover its CNSide CSF assay. This deal adds approximately 27.3 million covered lives to CNSide's network, bringing the total contracted coverage to roughly 153 million patients. This milestone allows the company to exceed its full-year 2026 target of 150 million covered lives ahead of schedule.YahooPlus Therapeutics Announces Scientific Presentations and Sponsored Symposium at 2026 SNO/ASCO CNS Metastases ConferencePlus Therapeutics, Inc. announced it will present two posters at the 2026 SNO/ASCO CNS Metastases Conference in Boston, highlighting its ReSPECT-LM clinical development program and CNSide® cerebrospinal fluid diagnostic platform. The company and its wholly owned subsidiary CNSide Diagnostics will also host a sponsored symposium on leptomeningeal metastases management. Additionally, Plus Therapeutics revealed it will formally introduce Cerenome as its new corporate identity alongside new branding for its expanded CNS cancer focus at the conference.