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Chosa Oncology

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uuid00027j8

Namestring
Chosa Oncology
Legal namestring
CHOSA Oncology AB
Websiteurl
chosa.bio
Company typeenum
Private
Founded yearstring
-
Descriptiontext

CHOSA Oncology AB is a Swedish-domiciled precision oncology company (Org.no. 559037-2271) developing Platin-DRP®, a 205-gene biomarker signature test designed to predict which solid-tumor patients are most likely to benefit from platinum-based chemotherapy (cisplatin or carboplatin). The test analyzes gene expression from a routine biopsy and generates a score estimating platinum sensitivity, with validation derived from the Phase III SPLENDOUR trial (ETOP/EORTC) in 82 advanced NSCLC patients showing statistically significant PFS (HR 0.697, p=0.029) and OS (HR 0.602, p=0.011) advantages for high-scoring patients, and median OS of 16.9 months versus 5.5 months for low scorers. The company has additionally validated the assay on the NanoString platform and presented breast cancer combination data with AIDA at ASCO 2026 showing up to 78% pathological complete response rates.

The company is headquartered at Ole Maaløes Vej 3 in Copenhagen, with a Swedish registered office in Malmö (c/o ECIT Services) and a 2026-established US presence in Boston/Cambridge (1 Broadway, MA 02142). It is publicly listed (Frankfurt: W5L) but operates with only 1-10 employees, reflecting a virtual model that relies on an externalized ecosystem: ETOP and EORTC for clinical trial infrastructure, NanoString for platform execution, AIDA for breast cancer co-development, and seven named KOLs across lung, breast, bladder, and endometrial cancer for scientific credibility. Founder and CEO is Peter Buhl Jensen.

Commercially, CHOSA is pre-revenue with no disclosed paying customers or pricing; its stated revenue model is biomarker test sales and licensing to healthcare systems, hospitals, clinical laboratories, and pharmaceutical partners. Go-to-market focuses on evidence-based selling through scientific conferences (ESMO, ASCO, European Lung Cancer Congress), webinars, investor relations communications, and direct healthcare system engagement. Capital formation has been via a Rights Issue in 2025 and an approximately $354,624 raise in June 2025, supporting the move into US commercialization of Platin-DRP.

Short descriptiontext

CHOSA Oncology is a Swedish-Domiciled precision oncology company developing Platin-DRP®, a 205-gene biomarker test that predicts which solid-tumor patients will benefit from cisplatin or carboplatin chemotherapy, serving oncologists, hospitals, and pharmaceutical partners.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersLund, Sweden
HQ citystring
Lund
HQ countrystring
Sweden
HQ regionstring
Europe
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
precision oncology diagnostics, biomarker test development, platinum chemotherapy selection, gene expression analysis, cancer treatment stratification
Industry2 codes
1Proteomics & Biomarker Analytical Testing
CodeHLAGADAGPrimaryYes
2Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays)
CodeHLAAAMACPrimaryNo
NAICS code1 code
  • In-Vitro Diagnostic Substance Manufacturing325413
SIC code1 code
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Precision Oncology Diagnostics
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Biomarker Test Sales/Licensing
TypeLicensing Royalties
Description

Revenue generated from sales or licensing of the Platin-DRP® biomarker test to healthcare systems, hospitals, and clinical laboratories. The test is used to guide platinum treatment decisions in oncology.

chosaoncology.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Platin-DRP®
Description

A biomarker test designed to predict which patients are most likely to benefit from cisplatin or carboplatin treatment. The 205-gene biomarker signature generates a score estimating a patient's likelihood of benefiting from platinum-based therapy.

chosaoncology.com
Core offering1 text field

CHOSA Oncology offers the Platin-DRP® biomarker test, a 205-gene gene expression signature analyzed from routine tumor biopsies that produces a score estimating a patient's likelihood of benefiting from platinum-based chemotherapy (cisplatin or carboplatin). The test is designed to guide oncology treatment decisions and is compatible with the NanoString clinical laboratory platform. Revenue is generated through sales or licensing of the test to healthcare systems, hospitals, and clinical laboratories.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • HR 0.697 (p=0.029) improvement in progression-free survival for high Platin-DRP® scores vs low scores
+3 more records
Product overview1 text field

CHOSA Oncology offers a single core product: Platin-DRP®, a precision oncology biomarker test designed to predict patient response to platinum-based chemotherapy. The test analyzes a 205-gene expression signature from routine biopsies to generate scores indicating which patients are most likely to benefit from cisplatin or carboplatin treatment. The product is primarily focused on lung cancer (NSCLC) with validation studies in breast cancer, and aims to improve response rates while reducing unnecessary toxicity exposure.

Product and service1 record
1Platin-DRP®
CategoryPrecision Oncology Diagnostics
Description

A 205-gene biomarker signature test that analyzes gene expression from routine tumor biopsies to generate a score estimating a patient's likelihood of benefiting from platinum-based chemotherapy (cisplatin or carboplatin). Designed for oncologists, hospitals, cancer treatment centers, and pharmaceutical partners developing platinum-based oncology regimens.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-01
Description

CHOSA and AIDA collaborated to present data at ASCO 2026 showing up to 78% pathological complete response (pCR) rate in breast cancer using combined, integrated, taxane and platinum biomarkers. This partnership combines biomarker expertise to advance precision oncology in breast cancer treatment.

2ETOP (European Thoracic Oncology Platform)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-01
Description

ETOP collaborated with EORTC on the Phase III SPLENDOUR trial, from which CHOSA's Platin-DRP® biomarker data was derived through translational analysis. This partnership provided the clinical evidence base for the biomarker validation.

news.cision.com
Strategic tierCoreTypeStrategic or Co-development Partner
Description

EORTC partnered with ETOP on the Phase III SPLENDOUR trial in advanced non-small cell lung cancer, providing the clinical trial infrastructure and patient population for Platin-DRP® validation.

Strategic tierCoreTypeTechnology or Integration
Description

NanoString platform has been validated for running Platin-DRP® tests, demonstrating significant overall survival prediction in Phase III lung cancer studies. This integration enables the test to run on standardized clinical laboratory equipment.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Natera commercializes Signatera (MRD) and other oncology molecular tests for treatment monitoring and recurrence detection. Comparable as a precision oncology molecular diagnostics company monetizing biomarker tests through clinical channels.

TypeDirect peer
Description

Foundation Medicine offers comprehensive genomic profiling tests (FoundationOne CDx) widely used to guide oncology treatment selection. A direct peer in molecular tumor profiling, with substantially greater scale and commercial reach.

TypeDirect peer
Description

Veracyte develops and commercializes genomic tests that resolve diagnostic ambiguity in oncology (e.g., Afirma, Percepta, Decipher). Directly comparable as a molecular diagnostics company selling biomarker tests into oncology clinical workflows.

TypeDirect peer
Description

NeoGenomics provides oncology-focused clinical laboratory and molecular testing services used to guide treatment decisions. Directly comparable as a clinical lab and molecular diagnostics provider in oncology.

TypeEmerging player
Description

Strata Oncology develops tumor profiling and precision oncology enrollment programs for biomarker-driven therapy selection. An emerging peer with similar biomarker-guided treatment selection focus, though smaller and at an earlier commercial stage.

TypeDirect peer
Description

Caris offers MI Profile and other molecular profiling assays used to inform oncology therapy selection. Directly comparable as a precision oncology profiling company monetizing biomarker-based decision support.

TypeDirect peer
Description

Exact Sciences commercializes Oncotype DX and other genomic tests that guide oncology treatment decisions. Directly comparable as a molecular diagnostic company with established oncology test sales channels.

TypeDirect peer
Description

Guardant Health offers liquid biopsy-based oncology tests (Guardant360, Guardant Reveal) that inform treatment selection. Comparable as a precision oncology molecular diagnostics company, though focused on liquid biopsy rather than tissue gene-expression biomarkers.

TypeDirect peer
Description

Personalis provides tumor genomic profiling (NeXT Personal) used for ultra-sensitive cancer detection and treatment monitoring. Directly comparable as a smaller oncology molecular profiling peer focused on biomarker-driven decision support.

TypeDirect peer
Description

Myriad sells predictive genetic/molecular tests (BRACAnalysis, Prolaris, myChoice) that guide oncology treatment decisions. Directly comparable as a precision oncology diagnostic company monetizing tests through clinical laboratories and licensing.

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 risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

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

Ideal customer profile2 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 capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 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 →

Chosa Oncology

Precision Oncology Diagnosticschosa.bio

CHOSA Oncology is a Swedish-Domiciled precision oncology company developing Platin-DRP®, a 205-gene biomarker test that predicts which solid-tumor patients will benefit from cisplatin or carboplatin chemotherapy, serving oncologists, hospitals, and pharmaceutical partners.

What Chosa Oncology does

CHOSA Oncology AB is a Swedish-domiciled precision oncology company (Org.no. 559037-2271) developing Platin-DRP®, a 205-gene biomarker signature test designed to predict which solid-tumor patients are most likely to benefit from platinum-based chemotherapy (cisplatin or carboplatin). The test analyzes gene expression from a routine biopsy and generates a score estimating platinum sensitivity, with validation derived from the Phase III SPLENDOUR trial (ETOP/EORTC) in 82 advanced NSCLC patients showing statistically significant PFS (HR 0.697, p=0.029) and OS (HR 0.602, p=0.011) advantages for high-scoring patients, and median OS of 16.9 months versus 5.5 months for low scorers. The company has additionally validated the assay on the NanoString platform and presented breast cancer combination data with AIDA at ASCO 2026 showing up to 78% pathological complete response rates.

The company is headquartered at Ole Maaløes Vej 3 in Copenhagen, with a Swedish registered office in Malmö (c/o ECIT Services) and a 2026-established US presence in Boston/Cambridge (1 Broadway, MA 02142). It is publicly listed (Frankfurt: W5L) but operates with only 1-10 employees, reflecting a virtual model that relies on an externalized ecosystem: ETOP and EORTC for clinical trial infrastructure, NanoString for platform execution, AIDA for breast cancer co-development, and seven named KOLs across lung, breast, bladder, and endometrial cancer for scientific credibility. Founder and CEO is Peter Buhl Jensen.

Commercially, CHOSA is pre-revenue with no disclosed paying customers or pricing; its stated revenue model is biomarker test sales and licensing to healthcare systems, hospitals, clinical laboratories, and pharmaceutical partners. Go-to-market focuses on evidence-based selling through scientific conferences (ESMO, ASCO, European Lung Cancer Congress), webinars, investor relations communications, and direct healthcare system engagement. Capital formation has been via a Rights Issue in 2025 and an approximately $354,624 raise in June 2025, supporting the move into US commercialization of Platin-DRP.

Chosa Oncology firmographics

Firmographics
Name
Chosa Oncology
Legal name
CHOSA Oncology AB
Website
https://chosa.bio
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
CHOSA Oncology is a Swedish-Domiciled precision oncology company developing Platin-DRP®, a 205-gene biomarker test that predicts which solid-tumor patients will benefit from cisplatin or carboplatin chemotherapy, serving oncologists, hospitals, and pharmaceutical partners.
Ownership category
akta.pro rank

Chosa Oncology industry classification

Industry
Product category
Precision Oncology Diagnostics
NAICS
In-Vitro Diagnostic Substance Manufacturing (325413)
SIC
In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Proteomics & Biomarker Analytical Testing (HLAGADAG)
akta.pro secondary industry
Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays) (HLAAAMAC)

Keywords

  • Precision oncology diagnostics
  • Biomarker test development
  • Platinum chemotherapy selection
  • Gene expression analysis
  • Cancer treatment stratification

Where Chosa Oncology is headquartered

Location

Headquarters

HQ city
Lund
HQ country
Sweden
HQ region
Europe

Offices3 records

Markets served

Chosa Oncology business model

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

Revenue model

  1. Biomarker Test Sales/Licensing: Revenue generated from sales or licensing of the Platin-DRP® biomarker test to healthcare systems, hospitals, and clinical laboratories. The test is used to guide platinum treatment decisions in oncology.

Go-to-market motion1 record

Distribution channels2 records

Marketing channels4 records

Chosa Oncology product offering

Product offering

Core offering

CHOSA Oncology offers the Platin-DRP® biomarker test, a 205-gene gene expression signature analyzed from routine tumor biopsies that produces a score estimating a patient's likelihood of benefiting from platinum-based chemotherapy (cisplatin or carboplatin). The test is designed to guide oncology treatment decisions and is compatible with the NanoString clinical laboratory platform. Revenue is generated through sales or licensing of the test to healthcare systems, hospitals, and clinical laboratories.

Product overview

CHOSA Oncology offers a single core product: Platin-DRP®, a precision oncology biomarker test designed to predict patient response to platinum-based chemotherapy. The test analyzes a 205-gene expression signature from routine biopsies to generate scores indicating which patients are most likely to benefit from cisplatin or carboplatin treatment. The product is primarily focused on lung cancer (NSCLC) with validation studies in breast cancer, and aims to improve response rates while reducing unnecessary toxicity exposure.

Differentiator

Problem solved

Functional benefit

Brands

  • Platin-DRP®: A biomarker test designed to predict which patients are most likely to benefit from cisplatin or carboplatin treatment. The 205-gene biomarker signature generates a score estimating a patient's likelihood of benefiting from platinum-based therapy.

Products and services

  • Platin-DRP® A 205-gene biomarker signature test that analyzes gene expression from routine tumor biopsies to generate a score estimating a patient's likelihood of benefiting from platinum-based chemotherapy (cisplatin or carboplatin). Designed for oncologists, hospitals, cancer treatment centers, and pharmaceutical partners developing platinum-based oncology regimens.

Quantifiable outcome

  • HR 0.697 (p=0.029) improvement in progression-free survival for high Platin-DRP® scores vs low scores
  • +3 more outcomes

Companies that use Chosa Oncology

Customer profile

Segments3 records

Ideal customer profiles2 records

Chosa Oncology technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature3 records

Chosa Oncology partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core.

  • AIDAcoreStrategic or Co-development Partner · 1 January 2026CHOSA and AIDA collaborated to present data at ASCO 2026 showing up to 78% pathological complete response (pCR) rate in breast cancer using combined, integrated, taxane and platinum biomarkers. This partnership combines biomarker expertise to advance precision oncology in breast cancer treatment.
  • ETOP (European Thoracic Oncology Platform)coreStrategic or Co-development Partner · 1 January 2026ETOP collaborated with EORTC on the Phase III SPLENDOUR trial, from which CHOSA's Platin-DRP® biomarker data was derived through translational analysis. This partnership provided the clinical evidence base for the biomarker validation.
  • EORTC (European Organisation for Research and Treatment of Cancer)coreStrategic or Co-development PartnerEORTC partnered with ETOP on the Phase III SPLENDOUR trial in advanced non-small cell lung cancer, providing the clinical trial infrastructure and patient population for Platin-DRP® validation.
  • NanoString TechnologiescoreTechnology or IntegrationNanoString platform has been validated for running Platin-DRP® tests, demonstrating significant overall survival prediction in Phase III lung cancer studies. This integration enables the test to run on standardized clinical laboratory equipment.

Scale indicators6 records

Recent moves7 records

Expansion highlights6 records

Chosa Oncology competitors and assessment

Company assessment

Direct peers

  • Natera: Natera commercializes Signatera (MRD) and other oncology molecular tests for treatment monitoring and recurrence detection. Comparable as a precision oncology molecular diagnostics company monetizing biomarker tests through clinical channels.
  • Foundation Medicine: Foundation Medicine offers comprehensive genomic profiling tests (FoundationOne CDx) widely used to guide oncology treatment selection. A direct peer in molecular tumor profiling, with substantially greater scale and commercial reach.
  • Veracyte: Veracyte develops and commercializes genomic tests that resolve diagnostic ambiguity in oncology (e.g., Afirma, Percepta, Decipher). Directly comparable as a molecular diagnostics company selling biomarker tests into oncology clinical workflows.
  • NeoGenomics: NeoGenomics provides oncology-focused clinical laboratory and molecular testing services used to guide treatment decisions. Directly comparable as a clinical lab and molecular diagnostics provider in oncology.
  • Caris Life Sciences: Caris offers MI Profile and other molecular profiling assays used to inform oncology therapy selection. Directly comparable as a precision oncology profiling company monetizing biomarker-based decision support.
  • Exact Sciences: Exact Sciences commercializes Oncotype DX and other genomic tests that guide oncology treatment decisions. Directly comparable as a molecular diagnostic company with established oncology test sales channels.
  • Guardant Health: Guardant Health offers liquid biopsy-based oncology tests (Guardant360, Guardant Reveal) that inform treatment selection. Comparable as a precision oncology molecular diagnostics company, though focused on liquid biopsy rather than tissue gene-expression biomarkers.
  • Personalis: Personalis provides tumor genomic profiling (NeXT Personal) used for ultra-sensitive cancer detection and treatment monitoring. Directly comparable as a smaller oncology molecular profiling peer focused on biomarker-driven decision support.
  • Myriad Genetics: Myriad sells predictive genetic/molecular tests (BRACAnalysis, Prolaris, myChoice) that guide oncology treatment decisions. Directly comparable as a precision oncology diagnostic company monetizing tests through clinical laboratories and licensing.

Emerging players

  • Strata Oncology: Strata Oncology develops tumor profiling and precision oncology enrollment programs for biomarker-driven therapy selection. An emerging peer with similar biomarker-guided treatment selection focus, though smaller and at an earlier commercial stage.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Chosa Oncology social profiles

Digital presence

Chosa Oncology financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Chosa Oncology leadership team

Management profile

Number of profiles

Profiles1 record

Chosa Oncology funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors

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

Chosa Oncology 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 Chosa Oncology

What does Chosa Oncology do?

CHOSA Oncology offers the Platin-DRP® biomarker test, a 205-gene gene expression signature analyzed from routine tumor biopsies that produces a score estimating a patient's likelihood of benefiting from platinum-based chemotherapy (cisplatin or carboplatin). The test is designed to guide oncology treatment decisions and is compatible with the NanoString clinical laboratory platform. Revenue is generated through sales or licensing of the test to healthcare systems, hospitals, and clinical laboratories.

Is Chosa Oncology a public or private company?

Chosa Oncology is a private company. It is classified as public and is currently operating.

When was Chosa Oncology founded?

Chosa Oncology was founded in -1. It employs 1 to 10 people.

Where is Chosa Oncology based?

Chosa Oncology is headquartered in Lund, Sweden, in the Europe region.

How does Chosa Oncology make money?

One revenue line is on record: biomarker Test Sales/Licensing.

Who are Chosa Oncology's main competitors?

Direct peers on record are Natera, Foundation Medicine, Veracyte, NeoGenomics, Caris Life Sciences, Exact Sciences, Guardant Health, Personalis and Myriad Genetics. Strata Oncology is listed as an emerging player.

Does Chosa Oncology have an API?

No public API is recorded for Chosa Oncology.

What industry is Chosa Oncology in?

Chosa Oncology's product category is Precision Oncology Diagnostics. Its primary akta.pro industry code is HLAGADAG, Proteomics & Biomarker Analytical Testing, with a secondary code of HLAAAMAC, Clinical Biomarker Testing Services (central labs, trial enrollment/monitoring assays). Its NAICS code is 325413 and its SIC code is 2835.

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Live signals
MarketScreenerChosa Oncology receives 94 tumor samples for validation of lung cancer testChosa Oncology received 94 tumor samples for validation of a lung cancer test. The SPLENDOUR study showed median survival of 16.9 months for high Platin-DRP scores versus 5.5 months for low scores. First results from Mount Sinai are expected in the first quarter of 2027.news.cision.comCHOSA Oncology accelerates value creation by entering into a commercially driven licensing agreement with Aida OncologyCHOSA Oncology and AIDA Oncology signed a global licensing agreement to bring CHOSA's Platin-DRP breast cancer predictor to AIDA's portfolio and AIDA's TaxaTect lung cancer predictor to CHOSA's. The non-exclusive deal grants each company rights to use the other's technology in its respective cancer type, with undisclosed per-test fees. The agreement builds on a joint study presented at ASCO 2026.MarketScreenerChosa recruits Bill Cronin for US expansionChosa Oncology AB has appointed Bill Cronin to lead its expansion efforts in the United States. The company specializes in developing immunotherapeutic drugs and vaccines for treating metastatic cancer.news.cision.comCHOSA Oncology appoints US commercialization Bill Cronin with a broad network in the oncology market, to accelerate launch of Platin-DRPCHOSA Oncology appointed Bill Cronin to lead its US commercialization of Platin-DRP, a platinum-response predictor. The appointment follows clinical data showing 16.9-month median overall survival for patients predicted to benefit versus 5.6 months for those not predicted to benefit. Cronin will support the planned RUO launch and future commercial expansion.ChosaoncologyCHOSA Oncology announces commencement of exercise period for TO2 warrants at the fixed price of SEK 0.78CHOSA Oncology began the exercise period for its TO2 warrants on 1 July 2026 at a fixed price of SEK 0.78 per share. The 7,951,740 warrants, if fully exercised, would raise approximately SEK 6.2 million before transaction costs. Proceeds will support CLIA certification and collaboration with Mount Sinai Hospital.news.cision.comCHOSA Oncology establishes US presence in Boston to support commercialization of Platin-DRPCHOSA Oncology established a Boston presence to support US commercialization of its Platin-DRP biomarker. The company will initially make the test available for Research Use Only to researchers and collaborators. It plans to explore predictive potential in carboplatin-treated lung cancer and platinum-PD-1 combinations.MarketScreenerChosa Oncology Sets Up Operations in Boston Ahead of U.S. Launch of Platin-DRPChosa Oncology is establishing Boston operations ahead of its U.S. launch of Platin-DRP. The company will initially offer the test as a research-use-only product for researchers, pharmaceutical companies, and clinical partners. CEO Peter Buhl Jensen calls the move an important milestone.news.cision.comCHOSA Oncology partners with Mount Sinai, New York to test biomarker guiding platin-immunotherapy in lung cancerCHOSA Oncology announced a collaboration with Mount Sinai to test its Platin-DRP biomarker in advanced non-small cell lung cancer patients receiving platinum chemotherapy with immunotherapy. The study aims to identify which patients benefit most, building on prior data showing 50% of patients may derive limited benefit. Results are expected to support continued development of Platin-DRP.news.cision.comCHOSA presents positive data on Platin-DRP® predicting overall survival in advanced NSCLC at the European Lung Cancer Congress 2026CHOSA Oncology AB presented positive data on its Platin-DRP® biomarker test at the European Lung Cancer Congress 2026 in Copenhagen, showing that higher scores were associated with statistically significant improvement in both progression-free survival (HR 0.697, p=0.029) and overall survival (HR 0.602, p=0.011) in 82 advanced NSCLC patients treated with platinum-based chemotherapy in the Phase III SPLENDOUR trial. Patients with high Platin-DRP® scores demonstrated median overall survival of 16.9 months compared to 5.5 months for those with low scores, with no significant interaction observed between the biomarker and cisplatin versus carboplatin treatment. The company stated the findings support further validation and regulatory development for Platin-DRP® as a predictive tool to guide platinum treatment in lung cancer.news.cision.comCHOSA to present Platin-DRP data predicting survival benefit from Carboplatin and Cisplatin in patients with advanced NSCLC from a Phase III study at the 2026 European Lung Cancer CongressSwedish biotech company CHOSA Oncology announced it will present Platin-DRP biomarker data at the 2026 European Lung Cancer Congress in Copenhagen on March 26, 2026, showing results from a translational analysis of patients from the ETOP/EORTC Phase III SPLENDOUR trial in advanced non-small cell lung cancer. The 205-gene biomarker signature is designed to predict which patients are most likely to benefit from carboplatin and cisplatin treatment, potentially offering clinicians a validated tool to guide platinum-based therapy selection in lung cancer.