
À propos de Cureety
Améliorer la prise en charge du cancer
En oncologie, les moments décisifs se jouent souvent loin de l'hôpital, entre deux consultations. Notre plateforme de soins de précision prolonge l'action des équipes soignantes avec un suivi personnalisé des symptômes, un repérage précoce des situations à risque et des outils de coordination.
Nous travaillons main dans la main avec les équipes soignantes et avec les acteurs de l'écosystème pour élargir l'accès aux soins de précision, et alléger le quotidien des patients, des aidants et des cliniciens. C'est ensemble que nous rendrons les soins en oncologie plus proactifs, plus précis et plus humains, à grande échelle.
La plateforme
Une plateforme entièrement au service de l'oncologie
Thérapies classiques ou avancées et télésurveillance réunies sur une même plateforme, avec un triage intelligent pour prioriser les patients.


01
Pour les professionnels de santé
Vous suivez vos patients entre deux consultations sans y passer vos journées. Notre télésurveillance personnalisée et cliniquement ciblée filtre le bruit des alertes et fait remonter ce qui compte vraiment. Vous passez d'une prise en charge réactive à une prise en charge proactive, avec un temps clinique mieux employé.
02
Pour l'industrie pharmaceutique et les sciences de la vie
Les données de vie réelle manquent souvent de continuité. Notre plateforme collecte des données longitudinales de qualité réglementaire sur la sécurité, la tolérance et l'état fonctionnel des patients. De quoi renforcer la rétention dans vos essais, documenter le profil de tolérance et alimenter le suivi post-commercialisation.
03
Pour la recherche clinique
Vous accédez à une vision fine du parcours patient, nourrie par des données recueillies hors du cadre des essais, au plus près du quotidien. Cette matière permet de mieux caractériser la toxicité des traitements et son impact réel sur la qualité de vie.
04
Pour les patients et leurs proches
Vous n'êtes jamais seul. Entre deux rendez-vous, vous partagez vos symptômes et vos effets secondaires avec votre équipe médicale, qui garde un œil sur votre état et réagit si nécessaire. Vous restez informé et accompagné à chaque étape de votre parcours.
Expertise
Conçu pour les patients, développé par des experts, validé par la science.
Une équipe pilotée par le clinique, entre oncologues expérimentés et pionniers de la santé numérique. Notre conviction : à la médecine de précision doit répondre une télésurveillance de précision. L'avenir de la cancérologie tient moins au volume de données qu'à une intelligence clinique spécifique à chaque traitement.
Envergure mondiale
Approuvé par plus de 250 centres de lutte contre le cancer dans 5 pays, nous avons accompagné plus de 100 000 patients dans le monde, avec plus de 1 000 000 questionnaires spécifiques et un fort taux d'engagement des patients.
Rigueur clinique
Basé sur un algorithme validé avec une sensibilité de 95,8 % et une spécificité de 94,4 % pour les classifications critiques.
Excellence opérationnelle
Nous développons des infrastructures qui simplifient les processus complexes : validation HDJ, récupération de bio, plan personnalisé de soins… Pour faire gagner du temps médical aux équipes et améliorer la prise en charge des patients.
Co-conception
La co-conception est dans notre ADN
Nous sommes convaincus que les outils cliniques les plus efficaces naissent de la rencontre entre l'expertise professionnelle et le vécu des patients.
Nos comités scientifiques
Ils garantissent la rigueur clinique de notre solution, de nos contenus et de nos protocoles, en parfaite adéquation avec l'organisation réelle des services de soin.
Notre comité de patients
Il garantit que notre interface reste intuitive et aidante. Nous recueillons les symptômes en utilisant un langage à la fois objectif et accessible aux patients, que notre couche d'intelligence clinique évalue ensuite automatiquement selon les normes CTCAE pour favoriser des décisions cliniques précises.
Nos partenaires stratégiques et conseillers
Accès au marché, cadre réglementaire, politiques de santé : ils éclairent les terrains où se joue l'adoption réelle d'une innovation. Leur rôle est d'ancrer notre plateforme dans les systèmes de santé de façon durable, éthique et soutenable à grande échelle.
Comité scientifique Europe

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
Comité scientifique USA

Dr. Hope S. Rugo
M.D, FASCO
City of Hope
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).

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

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.

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.

Director Breast Center/Chief Breast Oncology M.D., M.P.H., FASCO
Yale School of Medicine
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 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.

MD, PhD, Associate Professor in the Department of Investigational Cancer Therapeutics
University of Texas MD Anderson Cancer Center
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 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.
Notre comité d'experts

Confiance
Un soin durable et une innovation éthique
En oncologie, une donnée n'est jamais un simple chiffre. Elle raconte l'histoire d'un patient. Nous appliquons les exigences les plus strictes en matière de protection des données et d'IA responsable, dans le respect du RGPD, de la norme ISO 13485 et de la norme ISO 27001, ainsi que du cadre HIPAA aux États-Unis. Qu'il s'agisse d'un essai clinique international ou d'un centre de proximité, chaque donnée est traitée avec la transparence et la sécurité que la médecine d'aujourd'hui impose.
Réseau
Partenaires stratégiques
Carrières
Aidez-nous à redéfinir le standard de soins
Vous venez de la santé numérique ou de l'oncologie, et vous cherchez un poste où votre travail se mesure à ce qu'il change pour les patients. Nous construisons la télésurveillance de demain, avec des équipes soignantes exigeantes et des patients qui comptent sur nous. Si ce terrain vous parle, écrivez-nous.

Comité scientifique
Lorem ipsum
Lorem ipsum
Hôpital de la Pitié Salpêtrière - AP-HP
Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur.
Basé en
France
01 / 09


















