
Sobre Cureety
Cerrando la brecha en la atención oncológica
En oncología, los momentos más críticos suelen ocurrir fuera de las paredes de la clínica. Cureety ayuda a los equipos asistenciales a ampliar su alcance clínico y humano a través de su plataforma de atención de precisión, que combina el seguimiento personalizado de síntomas, la detección temprana de riesgos y herramientas de coordinación asistencial.
La misión de Cureety es trabajar mano a mano con los equipos asistenciales y ayudar a conectar a los socios del ecosistema digital para ampliar colectivamente el acceso a una atención de precisión, mejorando al mismo tiempo la vida diaria de pacientes, cuidadores y médicos. Creemos que, juntos, podemos contribuir al futuro de la oncología, permitiendo una atención más proactiva, precisa y centrada en las personas a gran escala.
La plataforma
Una plataforma conectada para el ecosistema oncológico
Integramos tratamientos avanzados y supervisión del paciente mediante triaje oncológico inteligente.


01
Para proveedores de atención médica
Maximizamos el impacto de los equipos de atención médica mediante el monitoreo remoto de forma personalizada y clínicamente específica. Al pasar de una gestión reactiva a una proactiva, filtramos el ruido de las alertas para priorizar lo crítico, optimizando el tiempo clínico, protegiendo al personal del agotamiento y reduciendo eventos evitables.
02
Para ciencias de la vida y farmacéuticas
Cerramos la brecha de la evidencia en el mundo real. Nuestra plataforma captura datos longitudinales de calidad regulatoria, incluyendo seguridad, tolerabilidad y estado funcional, esenciales para mejorar la retención en ensayos, el monitoreo de seguridad y la vigilancia poscomercialización.
03
Para investigadores
Ofrecemos una visión detallada del recorrido del paciente mediante datos de alta fidelidad que reflejan la experiencia real fuera de los ensayos clínicos. Nuestro enfoque basado en datos permite obtener información más profunda sobre la toxicidad de los tratamientos y los resultados en la calidad de vida.
04
Para pacientes y cuidadores
Nunca está solo. Cureety es su compañero diario, que supervisa los síntomas en tiempo real y le brinda la orientación experta y la conexión necesarias para mantenerse informado y apoyado en cada paso del camino.
Experiencia
Diseñado por personas, desarrollado por expertos y validado por la ciencia.
Somos un equipo liderado por especialistas clínicos, veteranos de la oncología y pioneros en salud digital. Entendemos que la medicina de precisión requiere un seguimiento preciso. El futuro de la atención oncológica no consiste solo en obtener más datos, sino en contar con inteligencia clínica específica para cada terapia.
Alcance global
Con la confianza de más de 220 centros oncológicos y el apoyo a más de 70 000 pacientes en todo el mundo, con más de 950 000 cuestionarios específicos de terapia completados con un alto nivel de participación de los pacientes
Rigor clínico
Desarrollado sobre un algoritmo validado con una sensibilidad del 95,8 % y una especificidad del 94,4 % para clasificaciones críticas.
Excelencia operativa
Desarrollamos infraestructura que agiliza procesos complejos, desde la documentación automatizada de reembolsos hasta las verificaciones de preparación para infusiones remotas, ahorrando tiempo y salvando vidas.
Codiseño
El codiseño está en nuestro ADN
Creemos que las herramientas clínicas más eficaces se construyen en la intersección entre la experiencia profesional y la vivencia del paciente.
Nuestro Comité Científico
Garantizar el rigor clínico de nuestra solución, contenido y protocolos, y su integración en los flujos de trabajo reales
Nuestro comité de pacientes
Garantiza que nuestra interfaz sea intuitiva y de apoyo. Registramos los síntomas utilizando un lenguaje objetivo y accesible para el paciente, que nuestra capa de inteligencia clínica clasifica automáticamente según los estándares CTCAE para respaldar decisiones clínicas precisas.
Nuestros socios estratégicos y asesores
Garantiza que nuestra plataforma siga siendo una solución sostenible, ética y escalable para los sistemas de salud globales. Navegan por las complejidades del acceso al mercado y las políticas sanitarias para transformar la innovación clínica en un estándar de atención viable y a largo plazo.
Comité científico

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
Asesores médicos

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.
Asesores de negocio

Confianza
Atención sostenible, innovación ética
En oncología, los datos son más que números: son la historia de un paciente. Nos adherimos a los estándares globales más estrictos de protección de datos e IA ética, manteniendo un cumplimiento total con HIPAA, ISO 13485 e ISO 27001. Ya sea apoyando un ensayo clínico global o una clínica comunitaria local, garantizamos que los datos se manejen con la transparencia y seguridad que exige la medicina moderna.
Red
Socios estratégicos
Carreras
Ayúdanos a redefinir el estándar de atención
¿Eres un innovador en salud digital o un experto en oncología con vocación de impacto? En Cureety no solo trabajamos: resolvemos. Si estás listo para construir el futuro del monitoreo remoto y marcar una diferencia real en la atención oncológica global, queremos conocerte.

Comité científico
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.
Con sede en
Francia
01 / 09


















