Digital Monitoring of Self-reported Symptoms by Patients Treated With Cabozantinib Plus Nivolumab for Advanced Clear-cell Renal Carcinoma

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Francois Baclesse

About this trial

The aim of the study is to evaluate the impact of digital monitoring of self-reported symptoms (PROs) on the adjustment of treatment management in patients treated with cabozantinib plus nivolumab for advanced clear cell renal cell carcinoma (RCC) in real life during the first 3 months of combined treatment

Eligibility criteria

Qualifiers

Patient older than 18 years

Diagnosis of advanced/metastatic Renal Cell Carcinoma (RCC) with a clear-cell component

No prior systemic treatment for RCC

Physician-initiated decision prior to study enrollment to treat with cabozantinib and nivolumab in combination, in first line for advanced/metastatic RCC, according to approved local labels

Disqualifiers

Patient assessed by the investigator to be unable or unwilling to comply with the requirements of the protocol

Current participation in another clinical study and/or in an investigational program with any intervention that could possibly interfere with the treatment and impact this study

Patient with history of allergy or hypersensitivity to components of the study drugs

Patient with contraindication to the study drugs

Trial design

Treatments tested in this trial

  • cabozantinib and nivolumab

Treatment groups

83 Participants
are divided into 1 treatment group

Sponsors and collaborators