Nuestros estudios
Evidencia clínica, arraigada en el impacto del mundo real
Detrás de cada funcionalidad de la plataforma Cureety existe un conjunto de evidencia clínica. Nuestros estudios están diseñados junto a equipos de oncología, basados en datos del mundo real y validados mediante ciencia revisada por pares, para hacer que la atención oncológica sea más proactiva, precisa y centrada en las personas a gran escala.
Interventional • Organizational benefit
OPTIMACURE
Description
A prospective, randomized, open-label, multicentric study designed to evaluate the effectiveness of standard of care with Cureety (RPM), compared to the standard of care alone OPTIMA program, to reduce the number of outgoing telephone calls during the first 8 weeks of intravenous treatment. The OPTIMA oncology program streamlines chemotherapy prescription and preparation through a pre-treatment consultation or call, and blood tests conducted 2 days before the patient's infusion.
Participantes
192 pacientes • 3 centros
Interventional • Organizational benefit
MINERVA
Description
A prospective, randomized, open-label, single-centric study to assess the effectiveness of standard of care with Cureety, compared to standard of care alone, to reduce the duration and numbers of telephone calls during the first 4 months of oral or intravenous treatment.
Participantes
80 pacientes • 1 centros
Observationnal • Performance
POSITEA-VA
Description
A study to evaluate the diagnostic performance of the medical device Cureety TechCare by independent medical review.
Participantes
400 pacientes
Observationnal • Clinical benefit
SECUR-RADIO
Description
A study to assess the diagnostic performance of Cureety remote monitoring in patients undergoing radiotherapy of cancer by independent medical review.
Participantes
81 pacientes • 6 centros
Observationnal • State of Art
ARGOS II
Description
A database study to describe the use of Cureety remote monitoring in the real-world setting in France between Oct. 1st 2019 and March 31st 2026.
Participantes
48137 pacientes • 107 centros
Observationnal • State of Art
LUMINIS
Description
A database study to describe the use of Cureety remote monitoring in the real-world setting in Italy between Jul. 1st 2023 and March 31st 2025.
Participantes
1016 pacientes • 1 centros
Observationnal • State of Art
ARGOS I
Description
A database study to describe the use of Cureety remote monitoring in the real-world setting in France between Oct. 1st 2019 and March 31st 2024.
Participantes
6457 pacientes • 40 centros
Observationnal • Feasability
Connect Elderly Patient To Doctor
Description
A prospective, observational, monocentric, study to evaluate the use of Cureety in older patients compared to younger patients.
Participantes
117 pacientes • 1 centros
Observationnal • Feasability
Connect Patient To Doctor
Description
A prospective, observational, monocentric, single-arm study to assess the feasibility of monitoring cancer patient with Cureety.
Participantes
39 pacientes • 1 centros
Observationnal • Clinical benefit
SOCOM-QOL
Description
Observational, prospective, longitudinal and monocentric study: collect quality of life data after oncological breast surgery for 5 years.
Participantes
1500 pacientes • 1 centros
Interventional • Treatment-related outcomes
SISMIC
Description
A prospective, double-arm clinical trial to demonstrate the benefit of a condensed treatment schedule of hypofractionated stereotactic radiotherapy in patients with brain metastases from radioresistant primary tumors.
Participantes
264 pacientes • 12 centros
Observationnal • Treatment-related outcomes
TOLERATE
Description
A prospective, longitudinal study to define best therapeutic class or sequence for patients with neuroendocrine tumor, in real-world settings.
Participantes
1100 pacientes • 34 centros
Observationnal • RWE
ESPERANTO
Description
A multicentric, retrospective, non-interventional, cohort study to compare the safety and use of androgen receptor pathway inhibitors in men with metastatic hormone-sensitive prostate cancer using data from remote monitoring and medical files.
Participantes
500 pacientes • 16 centros
Interventional • Organizational benefit
CANIQOL
Description
An interventional, one-arm study to assess remote monitoring of patients using the Cabozantinib/Nivolumab combination in advanced, metastatic kidney cancer.
Participantes
80 pacientes • 18 centros
Observationnal • Feasability
PROTECTY
Description
A prospective, observational, monocentric study to measure compliance with the use of Cureety in patients with prostate cancer.
Participantes
61 pacientes • 1 centros














