ClinicalTrials.Veeva

Menu

Non-interventional Study of Cabozantinib in Adults With Advanced Renal Cell Carcinoma (CASSIOPE)

Ipsen logo

Ipsen

Status

Completed

Conditions

Renal Cell Carcinoma

Treatments

Other: Data collection

Study type

Observational

Funder types

Industry

Identifiers

NCT03419572
F-FR-60000-001
EUPAS19464 (Registry Identifier)

Details and patient eligibility

About

The objective of this study is to understand the utilization of cabozantinib in subjects with advanced renal cell carcinoma (RCC) following prior VEGF-targeted therapy in real life settings in terms of dose modifications due to adverse events (AEs) when used as a second line therapy or third and later line therapy. Other patterns of use of cabozantinib will also be described.

Full description

The study will follow the real-life management of patients in clinical practice. Visits will take place according to the study site's clinical practice. Cabozantinib is to be administered as directed by the investigator according to the study site's usual clinical practice and the Cabometyx™ Summary of Product Characteristics (SmPC).

Enrollment

689 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years old
  • Has a diagnosis of advanced RCC
  • Has received at least one prior VEGF-targeted therapy
  • For whom the treating physician has decided to start treatment with cabozantinib tablets prior to inclusion
  • No previous exposure to cabozantinib prior to inclusion
  • Not concurrently involved in an interventional study
  • Consents to participate in this noninterventional study

Exclusion criteria

  • There are no exclusion criteria for this study.

Trial design

689 participants in 2 patient groups

Second line therapy
Description:
Data collection
Treatment:
Other: Data collection
Third and later line therapy
Description:
Data collection
Treatment:
Other: Data collection

Trial contacts and locations

91

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems