About Cureety

Bridging the Gap in Cancer Care

In oncology, the most critical moments often occur outside clinic walls. Cureety helps care teams extend their clinical and human reach through its precision care platform that combines tailored symptom monitoring, early risk detection, and care coordination tools.

Cureety’s mission is to work hand-in-hand with care teams and to help join up partners in the digital ecosystem, to collectively expand access to precision care while improving daily life for patients, caregivers, and clinicians. We believe that together, we can help contribute to the future of oncology, enabling more proactive, precise, and human-centered care at scale.

The Platform

A Connected Platform for the Oncology Ecosystem

We integrate advanced treatment and patient supervision through intelligent oncology triage.

01

For Healthcare Providers

We maximize care teams impact by providing remote monitoring in a clinically specific and personalized way. By moving from reactive to proactive management, we filter out the alert noise to prioritize what’s critical—optimizing clinical time, protecting your staff from burnout, and reducing preventable downstream events.

02

For Life Sciences & Pharma

We close the real-world evidence gap. Our platform captures the longitudinal, regulatory-grade data, including safety, tolerability, and functional status, essential for improving trial retention, safety monitoring, and post-market surveillance.

03

For Researchers

We provide a granular look at the patient journey through high-fidelity data that reflects the representative patient experience outside of clinical trials. Our data-driven approach unlocks deeper insights into treatment toxicities and quality-of-life outcomes.

04

For Patients & Caregivers

You are never alone. Cureety is your daily partner, monitoring symptoms in real time and providing the expert guidance and connection needed to stay informed and supported every step of the way.

Expertise

Designed with people, engineered by experts, validated by science.

We are a clinically led team of oncology veterans and digital health pioneers. We understand that precision medicine requires precision monitoring. The future of cancer care isn’t just about more data, it’s about therapy-specific clinical intelligence.

Global Scale

Trustedby 220+ cancer centers, and supported over 70,000 patients globally with over 950,000 therapy-specific questionnaires completed with high patient engagement

Clinical Rigor

Built on a validated algorithm with 95.8% sensitivity and 94.4% specificity for critical classifications.

Operational Excellence

We build infrastructure that streamlines complex processes—from automated reimbursement documentation to remote infusion readiness checks—saving both time and lives.

François-Guirec Champoiseau

CEO / Co-founder

Hugo Breitweiller

Chief Product Officer / Co-Founder

Nicolas Bégin

General Manager

Dr. Maya Gutierrez

Chairman of the Scientific Committee

Misha Kaur

Chief Operating Officer

Charles Parnot

Chief Scientific Officer

Guillaume Gaud

Head of Life Sciences

Pascal Ognibene

Chief Technical Officer

Florent Darrault

Chief Marketing Officer

Co-Design

Co-Design is in Our DNA

We believe the most effective clinical tools are built at the intersection of professional expertise and patient lived experience.

Our Scientific Committee

Ensure the clinical rigor of our solution, content and protocols, and fit with realworkflows

Our Patient Committee

Ensures our interface is intuitive and supportive. We capture symptoms using objective, patient-friendly language, which our clinical intelligence layer then automatically grades against CTCAE standards to support precise clinical decisions.

Our Strategic Partners & Advisors

Ensures our platform remains a sustainable, ethical, and scalable solution for global health systems. They navigate the complexities of market access and health policy to transform clinical innovation into a viable, long-term standard of care.

Scientific Committee

Dr. Emeline Colomba

Medical Oncologist

University Hospital Martinique

Dr. Carole Helissey

Oncologist, Head of Clinical Research

Service de Santé des Armées

Dr. Jean-Baptiste Meric

Medical Oncologist

Centre Hospitalier de Bligny

Dr. Thomas Feutren

Radiation Oncologist

Centre de Cancérologie de la Porte Saint Cloud

Dr. Félix Blanc-Durand

Oncologist

Institut Gustave Roussy

Dr. Côme Bommier

Hematologist

Centre de Cancérologie de la Porte Saint Cloud

Dr. Anne Creisson

Oncologist, Head of DICPA

Centre Antoine Lacassagne

Dr. Audrey Faveyrial

Oncologist, Department Head

Centre François Baclesse

Pr. Cindy Neuzillet

Oncologist, Department Head

Paul Brousse AP-HP

Dr. Noémie Studer

Pain Medicine Physician, Director of Supportive Care

Hôpital Foch

Pr. Lise Boussemart

Onco-Dermatology

University Hospital Nantes

Dr. Berengère Gruson

Hematologist

Clinique de l'Europe

Dr. Romain Kokorian

Uro-Oncology

Clinique Mathilde

Dr. Mathieu Boone

Neuro-Oncologist

Regional University Hospital Amiens

Dr. Raphaël Serre

Radiation Oncologist

Hôpital Pitié-Salpêtrière

Dr. Damien Botsen

Medical Oncologist and Head of the Department of Medical Oncology

Institut Godinot

Dr. Guillaume Desiro

Oncologist, Head of PRIMO Unit

Institut de Cancérologie de Lorraine

Dr. Bertrand Mennecier

Thoracic Oncologist

Regional University Hospital Nancy

Dr. Hélène Gardeney

Hematologist

University Hospital Poitiers

Dr. Guillaume Buiret

Medical Coordinator, Clinical Research Unit

CH Valence

Medical Advisors

Dr. Hope S. Rugo

M.D, FASCO

City of Hope

Medical Advisory Board
Dr. Hope S. Rugo
M.D, FASCO
City of Hope
US

Hope S. Rugo is professor of medicine and the director of the breast oncology clinical trials program at the University of California at San Francisco, and an investigator of SPORE (Specialized Program of Research Excellence in Breast Cancer) in the Bay Area.

In 2014 Rugo chaired the advisory panel of OncLive's "Giants of Cancer Care" award program.

Rugo was lead investigator on research that investigated the hair-preserving properties of cold caps for patients undergoing chemotherapy.

Along with her studies she is also an active clinician who gives lectures internationally.

In 2025, Rugo was named division chief of breast medical oncology for City of Hope, a cancer treatment and research group.

Dr. Rugo served for the American Society of Clinical Oncology's Education Committee on the editorial board.

She also served as the co-chair of the Emerging Toxicities Study Group for MASCC (Multinational Association for Supportive Care in Cancer).

Dr. Philippe Spiess

Oncologist, Chief of Clinical Innovation

Moffitt Cancer Center

Medical Advisory Board
Dr. Philippe Spiess
Oncologist, Chief of Clinical Innovation
Moffitt Cancer Center
https://www.linkedin.com/in/philippe-spiess-2150003a/

Chief of Clinical Innovation, Assistant chief of Surgical Services, Senior Member Dept of GU Oncology Leadership Academy Graduate, 2017 Robert A. Good Honor Society (RGHS) USF Health Morsani College of Medicine, 2026

Deborah Boyle

Oncology Nurse Consultant & Educator, AOCN

Medical Advisory Board
Deborah Boyle
Oncology Nurse Consultant & Educator, AOCN
US
https://www.linkedin.com/in/debi-boyle-rn-msn-faan/

A graduate of Yale University with a Master’s degree specializing in oncology nursing, Deborah (Debi) Boyle MSN, RN, AOCNS®-Emerita, FAAN, is a longstanding member of the Oncology Nursing Society who has honored her with multiple awards for exemplary clinical practice, publishing, contributions to enhancing patient quality of life, expertise in psychosocial oncology, and lifetime achievement.

She has practiced as an Oncology Clinical Nurse Specialist in Comprehensive Cancer Centers and community oncology programs. A frequent speaker nationally and internationally, Debi has been an invited participant in numerous ASCO, NCI, and NAM initiatives. She is a Fellow of the American Academy of Nursing and the author of nearly 500 publications.

Dr. Vincent Ma

M.D., Assistant Professor

University of Wisconsin-Madison

Medical Advisory Board
Dr. Vincent Ma
M.D., Assistant Professor
University of Wisconsin-Madison
US
https://www.linkedin.com/in/vincent-ma-03911b1a5

Vincent T. Ma, MD is an Assistant Professor in the Department of Medicine at the University of Wisconsin School of Medicine and Public Health and a medical oncologist in the Division of Hematology, Medical Oncology and Palliative Care, with a faculty affiliation in the Department of Dermatology. He also serves as Co-Chair of the Big Ten Cancer Research Consortium Melanoma/Cutaneous Oncology Clinical Trial Working Group, Immuno-Oncology Therapeutics Lead in the UW Carbone Cancer Center Early Phase Oncology Therapeutics Program, and Faculty Lead for Non-Melanoma Advanced Cutaneous Malignancies.

Dr. Ma received his medical degree from the University of Nevada School of Medicine in Reno, Nevada. He completed his residency training at the University of Michigan Health System in Ann Arbor, Michigan, followed by a Hematology/Oncology fellowship at the University of Michigan Rogel Cancer Center.


Dr. Ma’s research focuses on optimizing therapeutic strategies for melanoma and other advanced cutaneous malignancies, with an emphasis on drug development involving immunotherapies, molecularly targeted agents, and peripheral blood biomarker discovery. He also has a research interest in the recognition and management of immune-related adverse events associated with immune checkpoint inhibitor (ICI) therapy and is a co-founder of the UW Immune Checkpoint Inhibitor Toxicity Initiative Working Group.


Dr. Ma’s research focuses on optimizing therapeutic strategies for melanoma and other advanced skin cancers, with an emphasis on early-phase clinical trials evaluating immunotherapies and molecularly targeted agents. He has extensive clinical trial experience as a principal and sub-investigator on cooperative group and industry-sponsored studies and is an active member of the UW Carbone Cancer Center Early Phase Oncology Therapeutics Program, Phase 1 clinical trials group, and the Melanoma Disease-Oriented Team.

Dr. Maryam B. Lustberg

Director Breast Center/Chief Breast Oncology M.D., M.P.H., FASCO

Yale School of Medicine

Medical Advisory Board
Dr. Maryam B. Lustberg
Director Breast Center/Chief Breast Oncology M.D., M.P.H., FASCO
Yale School of Medicine
US
https://www.linkedin.com/in/maryam-lustberg-85578032/

Director Breast Center; Division Chief of Breast Oncology at Yale University School of Medicine/Yale Cancer Center; Professor of Internal Medicine (Medical Oncology)

Dr. Roy Beveridge

Consultant and Board Member, Medical Oncologist

Medical Advisory Board
Dr. Roy Beveridge
Consultant and Board Member, Medical Oncologist
US
https://www.linkedin.com/in/roy-beveridge-md-4629995/

Dr. Roy Beveridge is a physician executive with extensive leadership experience across clinical care, health systems, and payer organizations. A medical oncologist by training, he practiced for more than two decades, including in stem cell transplantation, before moving into senior executive roles. He has served as Chief Medical Officer at Humana and held leadership positions at US Oncology, McKesson Specialty Health, and Avalere Health, advising on clinical strategy, value-based care, and population health.

Dr. Beveridge brings a cross-sector perspective spanning providers, payers, and life sciences, with a focus on improving quality, access, and outcomes at scale. He has authored more than 200 publications and is a trusted advisor to healthcare organizations navigating an increasingly complex landscape.

Dr. Stéphane Champiat

MD, PhD, Associate Professor in the Department of Investigational Cancer Therapeutics

University of Texas MD Anderson Cancer Center

Medical Advisory Board
Dr. Stéphane Champiat
MD, PhD, Associate Professor in the Department of Investigational Cancer Therapeutics
University of Texas MD Anderson Cancer Center
US
https://www.linkedin.com/in/champiatstephane/

Stéphane Champiat, MD, PhD, is an Associate Professor in the Department of Investigational Cancer Therapeutics at The University of Texas MD Anderson Cancer Center. He is a medical oncologist specializing in early-phase drug development and cancer immunotherapy, with a particular focus on improving and accelerating drug development and patient access to innovative therapies.

Dr. Champiat completed his medical degree at Sorbonne University (formerly Paris VI University) and completed his residency in medical oncology at the University of Nantes, France. He subsequently obtained a PhD in Immunology from Paris-Saclay University and pursued postdoctoral research at the University of California, San Francisco.

Before joining MD Anderson in 2024, Dr. Champiat spent more than a decade at Gustave Roussy Cancer Center in France, where he led multiple Phase I immunotherapy trials and developed the iTOX program dedicated to the management of immune-related toxicities. He currently serves as principal or co-investigator on several early-phase clinical trials and is a member of the MD Anderson Immuno-Oncology Toxicity (IOTOX) Leaders’ Group.

Dr. Champiat has authored more than 100 peer-reviewed publications in leading oncology and immunotherapy journals.

Dr Julia Lai-Kwon

Medical Oncologist and Health Services Researcher

Peter MacCallum Cancer Centre

Medical Advisory Board
Dr Julia Lai-Kwon
Medical Oncologist and Health Services Researcher
Peter MacCallum Cancer Centre
US
https://www.linkedin.com/in/julia-lai-kwon-06146294/

Dr Julia Lai-Kwon is an early career Medical Oncologist and Health Services Researcher at Peter MacCallum Cancer Centre, Melbourne, Australia. Lai-Kwon previously trained at the Royal Marsden Hospital, United Kingdom, and the Melanoma Institute Australia. Dr Lai-Kwon’s clinical interests are melanoma and other cutaneous malignancies, and she is a sub-investigator on several sponsored and investigator-led clinical trials. Through her previous roles within the Drug Development Unit at the Royal Marsden and at the Melanoma Institute Australia, Dr. Lai-Kwon is skilled in the conduct and management of Phase 1-3 clinical trials.

Dr Lai-Kwon has research expertise inquality of life research, survivorship and patient-reported outcomes (PROs).  Dr Lai-Kwon was the Principal Investigator onseveral world-first studies examining the survivorship experience of peoplewith metastatic cancer treated with immunotherapy and targeted therapy, qualityof life issues in people with melanoma, and the use of patient-reportedoutcomes in clinical trials (including early phase clinical trials) and routinecancer care.  This work has been presentednationally and internationally and published in peer-reviewed publications.

Through this work, Dr Lai-Kwon has acquired skillsin the design, conduct, oversight and reporting of studies utilising bothqualitative, quantitative and mixed-method methodologies.  She has developed a particular focus on developingsupportive care interventions for people with metastatic cancer, including thedevelopment of novel stepped care models to manage fear of cancer recurrence orprogression in people with metastatic melanoma and the adaptation of the Cancerand Living Meaningfully (CALM) intervention for people living with metastaticnon-small cell lung cancer.  Throughthese projects, Dr Lai-Kwon has developed skills in collaborating withmultidisciplinary investigator teams and engaging with consumers throughout theresearch process.  


Dr Lai-Kwon is currently undertaking a PhD fundedby an NHMRC Postgraduate Scholarship under the supervision of Prof MichaelJefford, A/Prof Claudia Rutherford and A/Prof Stephanie Best on the co-designand implementation of digital symptom monitoring for people receivingimmunotherapy.  CI Lai-Kwon has evolvinginterests in the use of digital interventions to support people receivingsystemic therapies to self-monitor and manage and the use of implementationscience frameworks to guide the implementation of PROs in routine care.


Dr Lai-Kwon has >380 citations across 37 peer-reviewed publications, including first-author publications in high-impact journals, including the Journal of Clinical Oncology, the Journal for Immunotherapy of Cancer, and the European Journal of Cancer, as well as publications in The Lancet and Nature Communications. Dr. Lai-Kwon has been awarded $231,275.47 in grant funding as a principal investigator and $154,753 as an associate investigator. In the past five years, CILai-Kwon has been an invited speaker at national and international meetings, including the American Society of Clinical Oncology (ASCO), International Psycho-Oncology Society World Congress ,the Clinical Oncology Society of Australia.


Within Australia, CI Lai-Kwon’s evolving profile as a health services researcher is evidenced by her role as the Supportive Care and Survivorship Chapter Lead for the Australian Melanoma Management Guidelines and her membership of the Clinical Oncology Society of Australia PRO Working Group. Internationally, Dr. Lai-Kwon is an active member of the EORTC Quality of Life Group, including as a committee member of the Early Career Investigators Group, the International Society for Quality of Life Research (ISOQOL), and the Multinational Association for Supportive Care in Cancer (MASCC). Dr Lai-Kwon is currently contributing to the development of the EORTC advanced melanoma as part of an EORTC Quality of Life Group Visiting Fellowship to the Netherlands Cancer Institute and has previously contributed to the international validation of the anal cancer and survivorship modules. CI Lai-Kwon is a member of the Emerging Toxicity and Immunotherapy special interest groups within MASCC.  

Business Advisors

Bertrand Bégin

Venture capitalist

Pleiade Venture

Philippe Capart

Vice President of Business Development

Thermo Fisher Scientific

Tom Smith

Executive Managing Director

HealthTech Advisory Partners

Sebastien Marque

PhD, Cstat CEO co-founder

Horiana

Dr Philippe Souchois

M.D., Medical Director

Vivalto Sante group

Bruno Lempernesse

CEO

MDClone

Trust

Sustainable Care, Ethical Innovation

In oncology, data is more than just numbers, it is a patient’s story. We adhere to the strictest global standards for data protection and ethical AI, maintaining full HIPAA, ISO 13485, and ISO 27001 compliance. Whether supporting a global clinical trial or a local community clinic, we ensure data is handled with the transparency and security that modern medicine demands.

Network

Strategic partners

Judi

Expert Partner

AVBCC

Scientific Association

ACCC

Scientific Association

NCODA

Scientific Association

Careers

Help Us Rewrite the Standard of Care

Are you a digital health innovator or an oncology expert driven by impact? At Cureety, we don’t just work: we solve. If you’re ready to build the future of remote monitoring and make a tangible difference in global cancer care, we want to meet you.

Connect

Let’s Move Oncology Forward. Ready to Collaborate?

Our support team is here to help. Everyone is welcome, including patients, caregivers and patient associations.

Scientific Committee

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Hôpital de la Pitié Salpêtrière - AP-HP

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Based in

France

01 / 09