Our studies
Clinical evidence, rooted in real-world impact
Behind every feature of the Cureety platform stands a body of clinical evidence. Our studies are designed with oncology teams, built on real-world data, and validated through peer-reviewed science, to make oncology care more proactive, precise, and human-centered at scale.
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.
Participants
192 patients • 3 center(s)
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.
Participants
80 patients • 1 center(s)
Observationnal • Performance
POSITEA-VA
Description
A study to evaluate the diagnostic performance of the medical device Cureety TechCare by independent medical review.
Participants
400 patients
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.
Participants
81 patients • 6 center(s)
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.
Participants
48137 patients • 107 center(s)
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.
Participants
1016 patients • 1 center(s)
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.
Participants
6457 patients • 40 center(s)
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.
Participants
117 patients • 1 center(s)
Observationnal • Feasability
Connect Patient To Doctor
Description
A prospective, observational, monocentric, single-arm study to assess the feasibility of monitoring cancer patient with Cureety.
Participants
39 patients • 1 center(s)
Observationnal • Clinical benefit
SOCOM-QOL
Description
Observational, prospective, longitudinal and monocentric study: collect quality of life data after oncological breast surgery for 5 years.
Participants
1500 patients • 1 center(s)
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.
Participants
264 patients • 12 center(s)
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.
Participants
1100 patients • 34 center(s)
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.
Participants
500 patients • 16 center(s)
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.
Participants
80 patients • 18 center(s)
Observationnal • Feasability
PROTECTY
Description
A prospective, observational, monocentric study to measure compliance with the use of Cureety in patients with prostate cancer.
Participants
61 patients • 1 center(s)














