RecruitingNCT07314164

Study of Cabozantinib in Participants With Neuroendocrine Tumors Who Have Already Received Prior Treatment

CaboLife: A Prospective Non-Interventional Study on Effectiveness and Safety of Cabozantinib in Real-Life Setting for Previously Treated Patients With Neuroendocrine Tumour


Sponsor

Ipsen

Enrollment

150 participants

Start Date

Dec 17, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

This study will assess how well cabozantinib works and how safe it is in adults with a type of cancer called neuroendocrine tumors (NETs). These tumors can appear in all parts of the body. All participants in this study have already received at least one treatment that affects the whole body to help manage their cancer, but their disease has continued to grow. The study will take place in regular hospitals and clinics in Germany and Austria. It will follow about 150 participants who are taking cabozantinib as part of their usual care. Doctors will collect information from routine medical visits, tests, and scans to see how the cancer responds to treatment and how long participants stay on cabozantinib. They will also look at side effects and how the treatment affects participants' quality of life. This is an observational study, which means that no extra tests or procedures will be done beyond what is normally used to care for participants with this condition.


Eligibility

Min Age: 18 Years

Inclusion Criteria6

  • Participants can join the study if they meet all of the following conditions:
  • Are 18 years or older and able to give informed consent.
  • Have a physician-initiated decision to start treatment with cabozantinib for neuroendocrine tumors (NETs), made before joining the study.
  • Have unresectable or metastatic, well-differentiated pancreatic (pNET) or extra-pancreatic neuroendocrine tumors (epNET).
  • Have already received at least one prior systemic therapy, other than somatostatin analogues.
  • Have signed a written informed consent form.

Exclusion Criteria3

  • Participants cannot join the study if:
  • They are currently participating in an interventional clinical trial, or have done so within the last 3 months before joining this study.
  • They have a contraindication to cabozantinib treatment, based on the product's official prescribing information.

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Locations(28)

Medizinische Universitaet Graz

Graz, Austria

MVZ am Klinikum Aschaffenburg

Aschaffenburg, Germany

DRK Kliniken Berlin

Berlin, Germany

Evangelische Lungenklinik Berlin

Berlin, Germany

Krankenhaus St. Joseph-Stift Bremen GmbH

Bremen, Germany

Klinikum Chemnitz

Chemnitz, Germany

MVZ fuer Haematologie und Onkologie Koeln am Sachsenring

Cologne, Germany

pioh Studien und Mangement GbR

Cologne, Germany

Gemeinschaftspraxis Haematologie - Onkologie

Dresden, Germany

Technische Univiersitaet (TU) Dresden

Dresden, Germany

Universitaetsklinikum Essen

Essen, Germany

Krankenhaus Nordwest

Frankfurt, Germany

Uniklinikum Frankfurt

Frankfurt am Main, Germany

Universitaetsklinikum Giessen-Marburg

Giesen, Germany

Universitaetsmedizin Goettingen

Goettigen, Germany

Asklepios Kliniken Hamburg

Hamburg, Germany

Universitaetsklinikum Hamburg-Eppendorf

Hamburg, Germany

Studienzentrum UnterEms

Leer, Germany

MVZ Leipzig Mitte, MVZ Delitzsch

Leipzig, Germany

Universiteatsmedizin Leipzig

Leipzig, Germany

Kepler Universitaetsklinikum GmbH Linz

Linz, Germany

RKH Kliniken Ludwigsburg-Bietigheim gGmbH

Ludwigsburg, Germany

Philipps-Universitaet Marburg

Marburg, Germany

Johannes Wesling Klinikum Minden der Muehlenkreiskliniken AoeR

Minden, Germany

MVZ Muelheim an der Ruhr GmbH

Mülheim, Germany

Universitätsklinikum Tuebingen

Tübingen, Germany

Medizinische Studiengesellschaft Nord-West

Westerstede, Germany

Universitaetsklinikum Wuerzburg

Würzburg, Germany

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NCT07314164


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