RecruitingPhase IIEN originalKidney cancerMetastatic / advanced

Cabozantinib Dose Skipping as an Alternative to Dose Reductions

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

The goal of this study is to determine if an alternative cabozantinib dosing regimens results in a similar drug exposure compared to the standard regimens in patients with metastatic renal cell carcinoma (mRCC). All dosages of cabozantinib (20 ,40, 60mg) have the same price, and cabozantinib is eliminated very slowly by the body. This means that using fewer tablets could potentially lead to cost savings, while remaining equally effective. The main questions it aims to answer are: * Is the drug exposure from our experimental regimens similar to the standard dosing regimens? * Do the experimental regimens affect the number of side effect and the patients' quality of life? Participants will: * Take cabozantinib according to either the experimental or standard dosage regimen for 4 weeks * After 4 weeks: visit the clinic to collect some blood samples and complete two questionnaires. * 1 and 3 days after this visit: visit the clinic to collect 1 blood sample. * The day after the hospital visit: switch to the other dosing regimen and according to that regimen for another 4 weeks. * After 4 weeks: visit the clinic to collect some blood samples and complete two questionnaires * 1 and 3 days after this visit: visit the clinic to collect 1 blood sample.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Wiek co najmniej 18 lat
  • •Potwierdzony zaawansowany rak nerki
  • •Przyjmowanie cabozantinibu w dawce 20 lub 40 mg przez co najmniej 4 tygodnie
  • •Dobra tolerancja leku bez poważnych efektów ubocznych
  • •Ogólny stan zdrowia pozwalający na uczestnictwo w badaniu
  • •Oczekiwana długość życia co najmniej 6 miesięcy
  • •Zdolność do podpisania świadomej zgody

✗ Disqualifies

  • •Zaburzenia przewodu pokarmowego wpływające na wchłanianie leków
  • •Wcześniejsza rozległa operacja żołądka, trzustki, wątroby lub jelita
  • •Stosowanie leków, które znacząco zmieniają metabolizm cabozantinibu w ciągu ostatniego miesiąca
  • •Niemożność stosowania się do zalecanego zwykłego śniadania

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
August 31, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

LUMC

Leiden, Netherlands

Trial contact

Tom van der Hulle, MD PhD

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/1/2026.

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