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Atonco

Full company profile

uuid003f1cy

Namestring
Atonco
Legal namestring
Atonco SAS
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Atonco is a clinical-stage French radiopharmaceutical company founded in 2019 that develops astatine-211 (At-211) alpha-emitting radiopharmaceuticals for targeted alpha therapy in oncology. Its lead product, ATO-101™ ([211At]At-girentuximab), is composed of the anti-CAIX antibody girentuximab radiolabeled with astatine-211 and is administered via intravesical instillation for non-muscle-invasive bladder cancer (NMIBC) resistant to BCG immunotherapy and chemotherapy. The company's underlying technology exploits the 7.2-hour half-life and 5.9 MeV alpha emission of At-211, whose 55-80 µm tissue range (5-10 cell diameters) and ~100 keV/µm linear energy transfer enable selective destruction of residual tumor cells while sparing adjacent healthy tissue. Atonco operates under an exclusive license from Telix Pharmaceuticals for the girentuximab antibody and uses proprietary radiolabeling chemistry based on diaryliodonium salts developed in Nantes, France.

The company is pre-revenue and has no commercial product; ATO-101™ is investigational and used only within clinical trial frameworks. Atonco has no publicly disclosed pricing, and any future revenue will be generated through product sales upon regulatory approval, supplemented by licensing or royalty arrangements. The PERTINENCE Phase I feasibility study completed enrollment in 2022 with 6 patients. The PERSEVERANCE EU Phase I trial (NCT07260162) was authorized in France in December 2025 as the first clinical trial in France involving astatine-211, and a Phase 1-2a study is planned for 2026 at the University of Michigan. Atonco raised €4 million in September 2025, bringing total funding since inception to €10 million, and operates from the Bio-Ouest technology park in Saint-Herblain, France, with 11-50 employees.

Atonco's go-to-market is sales-led via clinical and academic partnerships. Named partners include Institut de Cancérologie de l'Ouest (ICO) as the principal clinical site in France, the University of Michigan as the US clinical collaborator, Telix Pharmaceuticals as the licensing partner for girentuximab, Ionetix as North American GMP manufacturing partner, Minerva Imaging as European GMP manufacturing partner, and GIP ARRONAX as the French At-211 production and process validation partner. Distribution is exclusively through clinical trial frameworks at partnered academic medical centers, with a Framatome/IBA MoU signed in February 2025 to build a future commercial At-211 cyclotron production network in Europe and the USA by 2027-2028.

Short descriptiontext

Atonco is a clinical-stage French radiopharmaceutical company developing ATO-101™, an astatine-211-labeled anti-CAIX antibody for non-muscle-invasive bladder cancer resistant to BCG and chemotherapy. It operates under a Telix license and conducts clinical trials in France and the US.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersSaint-herblain, France
HQ citystring
Saint-herblain
HQ countrystring
France
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
radiopharmaceutical development, targeted alpha therapy, cancer drug development, radiolabeled antibodies, clinical trial services
Industry4 codes
1Radiopharmaceutical CDMO & Manufacturing (GMP Fill-Finish)
CodeHLAIAGAFPrimaryYes
2Oncology & Hematology Pharmaceuticals
CodeHLAIAAACPrimaryNo
3Radiopharmaceutical Manufacturing & CDMO (Synthesis, GMP, Packaging, QA/QC)
CodeEUAKAIACPrimaryNo
4Urologic Oncology
CodeHLAKAOABPrimaryNo
NAICS code3 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical and Medicine Manufacturing3254
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Radiopharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Radiopharmaceutical Drug Development and Commercialization
TypeOne Time License
Description

Atonco is developing ATO-101™ as a radiopharmaceutical treatment for non-muscle-invasive bladder cancer. Revenue will be generated through future product sales upon regulatory approval. The company holds exclusive licensing from Telix Pharmaceuticals for girentuximab.

atonco-pharma.com
2Clinical Development Services
TypeLicensing Royalties
Description

The company conducts clinical trials in partnership with academic institutions and hospitals, with plans to commercialize once regulatory approvals are obtained.

atonco-pharma.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels5 records

Each record includes

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

Cost components6 values
Personnel, Technology or R&D, Operations, Supply Chain, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1ATO-101™
Description

Girentuximab radiolabelled with astatine-211 for non-muscle-invasive bladder cancer treatment

atonco-pharma.com
Core offering1 text field

Atonco is a clinical-stage radiopharmaceutical company developing ATO-101™, a candidate drug composed of girentuximab (anti-CAIX antibody) radiolabeled with the alpha-emitting radionuclide astatine-211 for targeted alpha immunotherapy of non-muscle-invasive bladder cancer (NMIBC) resistant to BCG and chemotherapy. The company focuses on preclinical research, radiochemistry, clinical development (Phase I PERSEVERANCE EU in France and Phase 1-2a planned at University of Michigan), and strategic partnerships for GMP manufacturing and commercialization. Future revenue is expected from product sales upon regulatory approval and from licensing arrangements with partners such as Telix Pharmaceuticals.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Phase I PERTINENCE study completed with 6 patients, demonstrating safety and excellent bladder retention of anti-CAIX antibody
+2 more records
Product overview1 text field

Atonco is a clinical-stage radiopharmaceutical company developing a single lead product, ATO-101™, based on girentuximab radiolabeled with astatine-211 for targeted alpha immunotherapy. The company focuses exclusively on alpha-immunotherapy using astatine-211 for cancers resistant to conventional treatments, with its primary indication being non-muscle-invasive bladder cancer (NMIBC).

Product and service1 record
1ATO-101™
CategoryRadiopharmaceutical therapy (targeted alpha immunotherapy)
Description

ATO-101™ ([211At]At-girentuximab) is a clinical-stage radiopharmaceutical candidate composed of the anti-CAIX antibody girentuximab radiolabeled with the alpha-emitting radionuclide astatine-211, intended for targeted alpha immunotherapy of non-muscle-invasive bladder cancer (NMIBC) resistant to BCG and chemotherapy. It is administered via intravesical instillation and is in Phase 1 clinical development.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2025-02-07
Description

Framatome and IBA signed MoU for strategic partnership to build Astatine-211 cyclotron production network in Europe and USA. First production facility planned in Pays de la Loire region (France) by 2027-2028. This supports future commercial supply of At-211 for Atonco and others.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2024-04-24
Description

Development agreement for GMP radiopharmaceutical production process validation of ATO-101™. GIP ARRONAX provides pharmaceutical development and GMP validation of manufacturing processes using their cyclotron for At-211 production. Builds on 15 years of At-211 development work.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-03-29
Description

Collaboration for Phase 1-2a clinical study of ATO-101™ in NMIBC. Led by Professor Benjamin Viglianti (Associate Professor of Clinical Radiology, Chief of Division of Nuclear Medicine) with Professor Peter Scott. Study pending FDA approval.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2023-10-31
Description

Collaboration for clinical dose production in Europe for planned Phase I clinical trial. Minerva Imaging sources At-211 from Rigshospitalet (Denmark). Partnership leverages Minerva's CDMO facility opened in 2023.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2022-03-31
Description

Partnership agreement for GMP manufacturing and supply of radiopharmaceutical product for clinical studies and US commercialization. Ionetix provides astatine-211 production capabilities and network of radiopharmacies. Covers FDA agent agreement signed in August 2021.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-12-21
Description

First patient dosed in PERTINENCE Phase I study at ICO, evaluating TLX250-CDx (girentuximab) in NMIBC patients as proof of concept for subsequent ATO-101™ therapy.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-05-19
Description

Clinical research partnership for the PERTINENCE feasibility study evaluating ⁸⁹Zr-girentuximab PET imaging and subsequent therapeutic use of astatine-211. Dr. Caroline Rousseau leads as Principal Investigator. ICO serves as trial sponsor and clinical site.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2019-12-09
Description

Licensing and development agreement allowing Atonco to use Telix's Molecularly Targeted Radiation (MTR) technology and select components from Telix's antibody portfolio (including girentuximab) for use with astatine-211 in bladder cancer treatment. Telix may receive approximately AUD 30 million in milestone payments plus royalties. Telix retains right to re-acquire program with compelling clinical data.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Centre de Recherche en Cancérologie et Immunologie Nantes-Angers, bringing together researchers and clinicians for cancer treatment discovery from fundamental biology to translational medicine. Team 2 conducted radiochemistry research leading to At-211 labeling methods.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

National competitiveness cluster bringing together biotherapy and radiopharmacy players for collaborative projects accelerating research to clinical application.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage actinium-225-based radiopharmaceutical company acquired by Bristol Myers Squibb in 2024 for ~$4.1B. Closest direct comparable in alpha-emitter oncology drug development with similar platform, regulatory, and supply-chain dynamics to Atonco.

TypeDirect peer
Description

Vertically integrated nuclear medicine company with manufacturing, radiopharmacy, and product operations across Europe and the US. Comparable on the radiopharmaceutical manufacturing and distribution side that Atonco accesses through partners.

TypeBroad incumbent
Description

Commercial-stage radiopharmaceutical company developing diagnostic and therapeutic agents. Direct licensor of girentuximab to Atonco and a strategic investor with a re-acquisition right; competes in the broader alpha/beta-emitting radiopharma space and would be the most likely acquirer.

TypeEmerging player
Description

Late-stage immunotherapy company with Anktiva (nogapendekin alfa) approved for BCG-unresponsive NMIBC. Competes with Atonco in the same patient population and could be a clinical development comparator or combination partner.

TypeDirect peer
Description

Clinical-stage developer of targeted alpha therapies using actinium-225 and linker technology. Acquired by AstraZeneca in 2024 for ~$2.4B, validating the strategic premium for alpha-emitting radioconjugates and serving as a direct category comparable to Atonco's At-211 program.

TypeBroad incumbent
Description

Owner of Lutathera and Pluvicto, the leading commercial radioligand therapies. Operates broadly in targeted radionuclide therapy with a global commercialization footprint that Atonco would rely on for partner or exit scenarios.

TypeDirect peer
Description

Emerging clinical-stage developer of alpha-emitting radioconjugates using proprietary miniprotein and peptidomimetic scaffolds. Direct competitor in targeted alpha therapy with a comparable early-stage, platform-driven profile to Atonco.

TypeDirect peer
Description

Clinical-stage radiopharmaceutical company developing therapeutic and diagnostic radionuclides including alpha emitters. Comparable as a European radiopharma developer with manufacturing infrastructure relevant to Atonco's isotope supply strategy.

TypeEmerging player
Description

Commercial-stage competitor in BCG-unresponsive NMIBC via Adstiladrin (nadofaragene). Direct therapeutic competitor in Atonco's lead indication and a benchmark for regulatory and commercial benchmarks in NMIBC.

TypeBroad incumbent
Description

Pioneer of alpha-emitting radiopharmaceuticals through Xofigo (Ra-223). Sets the precedent for commercial alpha-emitter therapeutics and operates an oncology/radiopharma pipeline relevant to At-211 programs.

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

Named customers1 record

Each record includes

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

Segment1 record

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 maturity
App detail

Has app

Feature4 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
No data
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 →

Atonco

Radiopharmaceuticalsatonco-pharma.com

Atonco is a clinical-stage French radiopharmaceutical company developing ATO-101™, an astatine-211-labeled anti-CAIX antibody for non-muscle-invasive bladder cancer resistant to BCG and chemotherapy. It operates under a Telix license and conducts clinical trials in France and the US.

What Atonco does

Atonco is a clinical-stage French radiopharmaceutical company founded in 2019 that develops astatine-211 (At-211) alpha-emitting radiopharmaceuticals for targeted alpha therapy in oncology. Its lead product, ATO-101™ ([211At]At-girentuximab), is composed of the anti-CAIX antibody girentuximab radiolabeled with astatine-211 and is administered via intravesical instillation for non-muscle-invasive bladder cancer (NMIBC) resistant to BCG immunotherapy and chemotherapy. The company's underlying technology exploits the 7.2-hour half-life and 5.9 MeV alpha emission of At-211, whose 55-80 µm tissue range (5-10 cell diameters) and ~100 keV/µm linear energy transfer enable selective destruction of residual tumor cells while sparing adjacent healthy tissue. Atonco operates under an exclusive license from Telix Pharmaceuticals for the girentuximab antibody and uses proprietary radiolabeling chemistry based on diaryliodonium salts developed in Nantes, France.

The company is pre-revenue and has no commercial product; ATO-101™ is investigational and used only within clinical trial frameworks. Atonco has no publicly disclosed pricing, and any future revenue will be generated through product sales upon regulatory approval, supplemented by licensing or royalty arrangements. The PERTINENCE Phase I feasibility study completed enrollment in 2022 with 6 patients. The PERSEVERANCE EU Phase I trial (NCT07260162) was authorized in France in December 2025 as the first clinical trial in France involving astatine-211, and a Phase 1-2a study is planned for 2026 at the University of Michigan. Atonco raised €4 million in September 2025, bringing total funding since inception to €10 million, and operates from the Bio-Ouest technology park in Saint-Herblain, France, with 11-50 employees.

Atonco's go-to-market is sales-led via clinical and academic partnerships. Named partners include Institut de Cancérologie de l'Ouest (ICO) as the principal clinical site in France, the University of Michigan as the US clinical collaborator, Telix Pharmaceuticals as the licensing partner for girentuximab, Ionetix as North American GMP manufacturing partner, Minerva Imaging as European GMP manufacturing partner, and GIP ARRONAX as the French At-211 production and process validation partner. Distribution is exclusively through clinical trial frameworks at partnered academic medical centers, with a Framatome/IBA MoU signed in February 2025 to build a future commercial At-211 cyclotron production network in Europe and the USA by 2027-2028.

Atonco firmographics

Firmographics
Name
Atonco
Legal name
Atonco SAS
Website
https://atonco-pharma.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
Atonco is a clinical-stage French radiopharmaceutical company developing ATO-101™, an astatine-211-labeled anti-CAIX antibody for non-muscle-invasive bladder cancer resistant to BCG and chemotherapy. It operates under a Telix license and conducts clinical trials in France and the US.
Ownership category
akta.pro rank

Atonco industry classification

Industry
Product category
Radiopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Radiopharmaceutical CDMO & Manufacturing (GMP Fill-Finish) (HLAIAGAF)
akta.pro secondary industries
Oncology & Hematology Pharmaceuticals (HLAIAAAC), Radiopharmaceutical Manufacturing & CDMO (Synthesis, GMP, Packaging, QA/QC) (EUAKAIAC), Urologic Oncology (HLAKAOAB)

Keywords

  • Radiopharmaceutical development
  • Targeted alpha therapy
  • Cancer drug development
  • Radiolabeled antibodies
  • Clinical trial services

Where Atonco is headquartered

Location

Headquarters

HQ city
Saint-herblain
HQ country
France
HQ region
Europe

Offices1 record

Markets served

Atonco business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Operations, Supply Chain, Marketing or Sales, Infrastructure

Revenue model

  1. Radiopharmaceutical Drug Development and Commercialization: Atonco is developing ATO-101™ as a radiopharmaceutical treatment for non-muscle-invasive bladder cancer. Revenue will be generated through future product sales upon regulatory approval. The company holds exclusive licensing from Telix Pharmaceuticals for girentuximab.
  2. Clinical Development Services: The company conducts clinical trials in partnership with academic institutions and hospitals, with plans to commercialize once regulatory approvals are obtained.

Go-to-market motion1 record

Distribution channels5 records

Marketing channels5 records

Atonco product offering

Product offering

Core offering

Atonco is a clinical-stage radiopharmaceutical company developing ATO-101™, a candidate drug composed of girentuximab (anti-CAIX antibody) radiolabeled with the alpha-emitting radionuclide astatine-211 for targeted alpha immunotherapy of non-muscle-invasive bladder cancer (NMIBC) resistant to BCG and chemotherapy. The company focuses on preclinical research, radiochemistry, clinical development (Phase I PERSEVERANCE EU in France and Phase 1-2a planned at University of Michigan), and strategic partnerships for GMP manufacturing and commercialization. Future revenue is expected from product sales upon regulatory approval and from licensing arrangements with partners such as Telix Pharmaceuticals.

Product overview

Atonco is a clinical-stage radiopharmaceutical company developing a single lead product, ATO-101™, based on girentuximab radiolabeled with astatine-211 for targeted alpha immunotherapy. The company focuses exclusively on alpha-immunotherapy using astatine-211 for cancers resistant to conventional treatments, with its primary indication being non-muscle-invasive bladder cancer (NMIBC).

Differentiator

Problem solved

Functional benefit

Brands

  • ATO-101™: Girentuximab radiolabelled with astatine-211 for non-muscle-invasive bladder cancer treatment

Products and services

  • ATO-101™ ATO-101™ ([211At]At-girentuximab) is a clinical-stage radiopharmaceutical candidate composed of the anti-CAIX antibody girentuximab radiolabeled with the alpha-emitting radionuclide astatine-211, intended for targeted alpha immunotherapy of non-muscle-invasive bladder cancer (NMIBC) resistant to BCG and chemotherapy. It is administered via intravesical instillation and is in Phase 1 clinical development.

Quantifiable outcome

  • Phase I PERTINENCE study completed with 6 patients, demonstrating safety and excellent bladder retention of anti-CAIX antibody
  • +2 more outcomes

Companies that use Atonco

Customer profile

Named customers1 record

Segments1 record

Ideal customer profiles2 records

Atonco technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Atonco partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered minor and core.

  • Framatome and IBAminorStrategic or Co-development Partner · 7 February 2025Framatome and IBA signed MoU for strategic partnership to build Astatine-211 cyclotron production network in Europe and USA. First production facility planned in Pays de la Loire region (France) by 2027-2028. This supports future commercial supply of At-211 for Atonco and others.
  • GIP ARRONAXcoreTechnology or Integration · 24 April 2024Development agreement for GMP radiopharmaceutical production process validation of ATO-101™. GIP ARRONAX provides pharmaceutical development and GMP validation of manufacturing processes using their cyclotron for At-211 production. Builds on 15 years of At-211 development work.
  • University of MichigancoreStrategic or Co-development Partner · 29 March 2024Collaboration for Phase 1-2a clinical study of ATO-101™ in NMIBC. Led by Professor Benjamin Viglianti (Associate Professor of Clinical Radiology, Chief of Division of Nuclear Medicine) with Professor Peter Scott. Study pending FDA approval.
  • Minerva ImagingcoreChannel Partner/ Reseller/ Distributor · 31 October 2023Collaboration for clinical dose production in Europe for planned Phase I clinical trial. Minerva Imaging sources At-211 from Rigshospitalet (Denmark). Partnership leverages Minerva's CDMO facility opened in 2023.
  • IonetixcoreChannel Partner/ Reseller/ Distributor · 31 March 2022Partnership agreement for GMP manufacturing and supply of radiopharmaceutical product for clinical studies and US commercialization. Ionetix provides astatine-211 production capabilities and network of radiopharmacies. Covers FDA agent agreement signed in August 2021.
  • Institut de Cancérologie de l'Ouest (ICO)coreStrategic or Co-development Partner · 21 December 2021First patient dosed in PERTINENCE Phase I study at ICO, evaluating TLX250-CDx (girentuximab) in NMIBC patients as proof of concept for subsequent ATO-101™ therapy.
  • Institut de Cancérologie de l'Ouest (ICO)coreStrategic or Co-development Partner · 19 May 2021Clinical research partnership for the PERTINENCE feasibility study evaluating ⁸⁹Zr-girentuximab PET imaging and subsequent therapeutic use of astatine-211. Dr. Caroline Rousseau leads as Principal Investigator. ICO serves as trial sponsor and clinical site.
  • Telix PharmaceuticalscoreOEM/ Whitelabel/ Licensing Partner · 9 December 2019Licensing and development agreement allowing Atonco to use Telix's Molecularly Targeted Radiation (MTR) technology and select components from Telix's antibody portfolio (including girentuximab) for use with astatine-211 in bladder cancer treatment. Telix may receive approximately AUD 30 million in milestone payments plus royalties. Telix retains right to re-acquire program with compelling clinical data.
  • CRCI2NAminorStrategic or Co-development PartnerCentre de Recherche en Cancérologie et Immunologie Nantes-Angers, bringing together researchers and clinicians for cancer treatment discovery from fundamental biology to translational medicine. Team 2 conducted radiochemistry research leading to At-211 labeling methods.
  • Atlanpole BiotherapiesminorStrategic or Co-development PartnerNational competitiveness cluster bringing together biotherapy and radiopharmacy players for collaborative projects accelerating research to clinical application.

Scale indicators4 records

Recent moves6 records

Expansion highlights6 records

Atonco competitors and assessment

Company assessment

Direct peers

  • RayzeBio: Clinical-stage actinium-225-based radiopharmaceutical company acquired by Bristol Myers Squibb in 2024 for ~$4.1B. Closest direct comparable in alpha-emitter oncology drug development with similar platform, regulatory, and supply-chain dynamics to Atonco.
  • Curium Pharma: Vertically integrated nuclear medicine company with manufacturing, radiopharmacy, and product operations across Europe and the US. Comparable on the radiopharmaceutical manufacturing and distribution side that Atonco accesses through partners.
  • Fusion Pharmaceuticals: Clinical-stage developer of targeted alpha therapies using actinium-225 and linker technology. Acquired by AstraZeneca in 2024 for ~$2.4B, validating the strategic premium for alpha-emitting radioconjugates and serving as a direct category comparable to Atonco's At-211 program.
  • Aktis Oncology: Emerging clinical-stage developer of alpha-emitting radioconjugates using proprietary miniprotein and peptidomimetic scaffolds. Direct competitor in targeted alpha therapy with a comparable early-stage, platform-driven profile to Atonco.
  • ITM Isotope Technologies Munich: Clinical-stage radiopharmaceutical company developing therapeutic and diagnostic radionuclides including alpha emitters. Comparable as a European radiopharma developer with manufacturing infrastructure relevant to Atonco's isotope supply strategy.

Broad incumbents

  • Telix Pharmaceuticals: Commercial-stage radiopharmaceutical company developing diagnostic and therapeutic agents. Direct licensor of girentuximab to Atonco and a strategic investor with a re-acquisition right; competes in the broader alpha/beta-emitting radiopharma space and would be the most likely acquirer.
  • Novartis (Advanced Accelerator Applications): Owner of Lutathera and Pluvicto, the leading commercial radioligand therapies. Operates broadly in targeted radionuclide therapy with a global commercialization footprint that Atonco would rely on for partner or exit scenarios.
  • Bayer (Algeta heritage): Pioneer of alpha-emitting radiopharmaceuticals through Xofigo (Ra-223). Sets the precedent for commercial alpha-emitter therapeutics and operates an oncology/radiopharma pipeline relevant to At-211 programs.

Emerging players

  • ImmunityBio: Late-stage immunotherapy company with Anktiva (nogapendekin alfa) approved for BCG-unresponsive NMIBC. Competes with Atonco in the same patient population and could be a clinical development comparator or combination partner.
  • Ferring Pharmaceuticals: Commercial-stage competitor in BCG-unresponsive NMIBC via Adstiladrin (nadofaragene). Direct therapeutic competitor in Atonco's lead indication and a benchmark for regulatory and commercial benchmarks in NMIBC.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Atonco social profiles

Digital presence

Atonco financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Atonco leadership team

Management profile

Number of profiles

Profiles7 records

Atonco funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Atonco 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 Atonco

What does Atonco do?

Atonco is a clinical-stage radiopharmaceutical company developing ATO-101™, a candidate drug composed of girentuximab (anti-CAIX antibody) radiolabeled with the alpha-emitting radionuclide astatine-211 for targeted alpha immunotherapy of non-muscle-invasive bladder cancer (NMIBC) resistant to BCG and chemotherapy. The company focuses on preclinical research, radiochemistry, clinical development (Phase I PERSEVERANCE EU in France and Phase 1-2a planned at University of Michigan), and strategic partnerships for GMP manufacturing and commercialization. Future revenue is expected from product sales upon regulatory approval and from licensing arrangements with partners such as Telix Pharmaceuticals.

Is Atonco a public or private company?

Atonco is a private company. It is classified as unknown and is currently operating.

When was Atonco founded?

Atonco was founded in 2019. It employs 1 to 10 people.

Where is Atonco based?

Atonco is headquartered in Saint-herblain, France, in the Europe region.

How does Atonco make money?

Two revenue lines are on record. Radiopharmaceutical Drug Development and Commercialization is the primary driver. The others are clinical Development Services.

Who are Atonco's main competitors?

Direct peers on record are RayzeBio, Curium Pharma, Fusion Pharmaceuticals, Aktis Oncology and ITM Isotope Technologies Munich. Broad incumbents are Telix Pharmaceuticals, Novartis (Advanced Accelerator Applications) and Bayer (Algeta heritage). Emerging players are ImmunityBio and Ferring Pharmaceuticals.

Does Atonco have an API?

No public API is recorded for Atonco.

What industry is Atonco in?

Atonco's product category is Radiopharmaceuticals. Its primary akta.pro industry code is HLAIAGAF, Radiopharmaceutical CDMO & Manufacturing (GMP Fill-Finish), with a secondary code of HLAIAAAC, Oncology & Hematology Pharmaceuticals. Its NAICS code is 541714 and its SIC code is 2834.

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