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Cabozantinib and Nivolumab among older patients with renal-cell carcinoma, a prospective cohort with geriatric, pharmacologic and patient-reported-outcome evaluation (CABOLD)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-516650-22-00
Acronym
2024/3873 CABOLD
Enrollment
50
Registered
2025-02-21
Start date
2025-05-16
Completion date
Unknown
Last updated
2025-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal carcinoma

Brief summary

Treatment patterns, including starting dose of Cabozantinib, dose interruption, dose modification related to all grade toxicity at 24 weeks.

Detailed description

Overall response rate based on radiological evaluation, Overall-survival, Progression free survival, Duration of response, Tolerance based on physicians and patients reports, Unplanned hospitalizations, emergency departments visits and falls, Patients reported quality of life (FACT-G and FACIT-TS-G),, Exploratory analyses to assess potential associations between G-CODE parameters and pharmacological monitoring of Cabozantinib with safety, efficacy, and QoL criteria

Interventions

DRUGOPDIVO 10 mg/mL concentrate for solution for infusion.

Sponsors

Institut Gustave Roussy
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Treatment patterns, including starting dose of Cabozantinib, dose interruption, dose modification related to all grade toxicity at 24 weeks.

Secondary

MeasureTime frame
Overall response rate based on radiological evaluation, Overall-survival, Progression free survival, Duration of response, Tolerance based on physicians and patients reports, Unplanned hospitalizations, emergency departments visits and falls, Patients reported quality of life (FACT-G and FACIT-TS-G),, Exploratory analyses to assess potential associations between G-CODE parameters and pharmacological monitoring of Cabozantinib with safety, efficacy, and QoL criteria

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026