I nostri studi
Evidenze cliniche, radicate nell'impatto reale
Dietro ogni funzionalità della piattaforma Cureety c'è un solido corpus di evidenze cliniche. I nostri studi sono progettati insieme ai team oncologici, basati su dati del mondo reale e validati da pubblicazioni scientifiche sottoposte a revisione paritaria, per rendere l'assistenza oncologica più proattiva, precisa e incentrata sulla persona, su larga scala.
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.
Partecipanti
192 pazienti • 3 centri
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.
Partecipanti
80 pazienti • 1 centri
Observationnal • Performance
POSITEA-VA
Description
A study to evaluate the diagnostic performance of the medical device Cureety TechCare by independent medical review.
Partecipanti
400 pazienti
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.
Partecipanti
81 pazienti • 6 centri
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.
Partecipanti
48137 pazienti • 107 centri
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.
Partecipanti
1016 pazienti • 1 centri
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.
Partecipanti
6457 pazienti • 40 centri
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.
Partecipanti
117 pazienti • 1 centri
Observationnal • Feasability
Connect Patient To Doctor
Description
A prospective, observational, monocentric, single-arm study to assess the feasibility of monitoring cancer patient with Cureety.
Partecipanti
39 pazienti • 1 centri
Observationnal • Clinical benefit
SOCOM-QOL
Description
Observational, prospective, longitudinal and monocentric study: collect quality of life data after oncological breast surgery for 5 years.
Partecipanti
1500 pazienti • 1 centri
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.
Partecipanti
264 pazienti • 12 centri
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.
Partecipanti
1100 pazienti • 34 centri
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.
Partecipanti
500 pazienti • 16 centri
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.
Partecipanti
80 pazienti • 18 centri
Observationnal • Feasability
PROTECTY
Description
A prospective, observational, monocentric study to measure compliance with the use of Cureety in patients with prostate cancer.
Partecipanti
61 pazienti • 1 centri














