Cureety
Cureety sells an oncology remote monitoring platform that turns patient reported symptoms into toxicity levels aligned with CTCAE and prioritizes the patients who need attention between visits. Protocols are written for specific therapies, including antibody drug conjugates, CAR T, bispecifics, oral therapies and radiotherapy; its medical device, Cureety TechCare, scores each report, and in the POSITEA-VA study the classification reached 95.8 percent sensitivity and 94.4 percent specificity for critical cases across more than 400 patients. Around the monitoring sit treatment calendars, readiness checks that combine lab results with toxicity reports before infusion, oral therapy adherence tracking, patient guidance aligned with NCCN and ASCO, and AI voice agents for patients with limited digital literacy or impaired vision.
Cureety reports more than 100,000 patients supported, more than 3,500 healthcare professionals and more than 250 cancer centers, across France, Belgium, Italy, Portugal, Spain and the United States. On 2 September 2026 it acquired Reimagine Care, the US oncology care company whose Remi assistant and care teams continue under their own name. François-Guirec Champoiseau is chief executive and co founder; the company is based in Paris, with Nashville named in the acquisition.
Capability Axes
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AI voice agents call patients who cannot use the app, extending monitoring to people with limited digital literacy or impaired vision. The core of the platform is the TechCare classification, which turns each symptom report into a CTCAE toxicity level with therapy specific scoring and prioritizes the patients who need attention.
Treatment calendars, readiness checks, adherence tracking and patient guidance are workflow software that stands on its own.
Clinicians act on what the platform surfaces. Each report is scored and prioritized so care teams see who needs attention, and Reimagine Care's assistant, now in the same group, escalates to human care teams when needed. Patients receive self management guidance between contacts.
Alert thresholds and how a clinician overrides a score are not described.
Therapy specific algorithms score symptoms against CTCAE and separate routine side effects from clinically relevant signals, and AI voice agents reach patients who cannot use the app. The classifier's performance is reported with sensitivity, specificity and false positive rate.
Whether the classification is a learned model or a scoring system, and which model runs the voice agents, are not named.
Cureety develops its therapy specific algorithms and protocols with oncologists, and the voice agents and Reimagine Care's Remi assistant sit in the same group after the September 2026 acquisition. Data supports research and drug development through partnerships with cancer centers.
The hosting provider and any outside model behind the voice agents are not named.
The POSITEA-VA study, run by independent medical review, reports that the classification correctly identified 95.8 percent of patients experts rated critical, with 94.4 percent specificity and 5.6 percent false positives across more than 400 patients, and Cureety describes it as peer reviewed. A separate study reports strong classification performance for radiotherapy patients, a real world analysis covers French use from October 2019 to March 2026, and more than a million questionnaires have been completed.
Outcome results such as avoided hospitalizations are not reported with a method.
The company describes full HIPAA, ISO 13485 and ISO 27001 compliance and says data is handled transparently for both trials and community clinics, and a US privacy notice and terms are published. Patient reports, lab results and adherence data flow through the platform and sync with the EHR.
Retention and whether patient data trains the models are not stated.
The platform is described as HIPAA compliant, and the company publishes a US privacy notice and US terms of use alongside its European sites for France, Belgium, Italy, Portugal and Spain. Since September 2026 its US group also includes Reimagine Care, which runs oncology care teams for US practices.
No business associate statement or agreement is published.
Full HIPAA, ISO 13485 and ISO 27001 compliance is the company's stated position, and the monitoring runs as a medical device under a quality management system. The platform serves global clinical trials as well as cancer centers and community clinics.
No ISO 27001 certificate, audit report or trust center is published.
TechCare, the classification engine, is described as a medical device, and its diagnostic performance was studied by independent medical review. The platform scores toxicity and prioritizes patients for clinical teams, and gives patients symptom guidance aligned with NCCN and ASCO.
Which jurisdictions TechCare is cleared or certified in, and its device class, are not stated.
Ethical AI is a stated commitment: the company says it follows the strictest global standards for ethical AI and data protection, and frames the voice agents as a way to reach patients with limited digital literacy or impaired vision. Its classifier was assessed against expert ratings.
No governance process or performance across patient groups, languages or therapies is published.
The classification's error rate is published with its method and sample: 95.8 percent sensitivity, 94.4 percent specificity and 5.6 percent false positives against independent expert review across more than 400 patients in POSITEA-VA. Clinicians review the prioritized list and decide on the next action.
No warranty or remediation commitment for a missed critical report is published.
Patient reminders and data sync with the institution's existing EHR, and the platform automatically combines lab results with patient toxicity reports for readiness checks before treatment. Treatment calendars coordinate blood tests and appointments across regimens.
No EHR vendor, interface standard or named integration is published.
The platform runs as a hosted service for cancer centers in five European countries and the United States, with patient apps, voice agents and EHR synchronization. Each pathway, cancer type and workflow is configured to the institution.
Hosting provider and data location for each country are not stated, including for French health data.
Cancer centers, community practices and trial sponsors request a demo, and Cureety frames the return around fewer avoidable hospitalizations and unscheduled calls, better infusion chair use and less drug waste from readiness checks. Since September 2026 it can pair the platform with Reimagine Care's US care teams.
Cureety's prices and contract terms are not public.
Oncology is the whole scope, organized by therapy rather than disease: protocols cover antibody drug conjugates, CAR T, bispecifics, oral therapies and radiotherapy, for academic centers, community clinics and clinical trials. Cureety reports more than 250 cancer centers and 100,000 patients across France, Belgium, Italy, Portugal, Spain and the United States, and real world data from France runs from October 2019 to March 2026.
Published studies cover the classification algorithm, including radiotherapy patients, rather than each therapy protocol.
Pricing
Vendor-published figures are labeled as such. Figures labeled “Estimated” are derived from third-party sources and have not been confirmed by the vendor.
| Entry Price | Pricing Basis | BAA Tier | Implementation | Source |
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Not published
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Sold to cancer centers, community practices and trial sponsors through demos. Rates are quoted to each center rather than published. | HIPAA compliance is stated; no business associate agreement is published. | Not published. Pathways, cancer types and workflows are configured for each institution. | Vendor Published |
Cureety frames value around fewer avoidable hospitalizations and unscheduled calls, better infusion chair use and less drug waste, and since September 2026 can add Reimagine Care's US care teams. Cureety publishes no price list.