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CABONEN – a phase II trial of Cabozantinib in patients with advanced, low proliferative NEN G3

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-510863-50-00
Acronym
02679
Enrollment
45
Registered
2024-08-30
Start date
2021-04-23
Completion date
Unknown
Last updated
2025-11-20

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

Conditions

Neuroendocrine Neoplasia Neuroendocrine Tumor

Brief summary

Disease control rate (DCR) 6 months after treatment start (Complete Response (CR) + Partial Response (PR) + Stable Disease (SD))

Detailed description

Disease control rate 3 and 12 months after treatment start, Objective response rate (ORR) 3 months after treatment start and best objective response rate, Progression free survival (PFS) and overall survival (OS), Time on drug (TOD), EORTC QLQ-C30 Quality of Life Questionnaire monthly for 12 months after treatment start and after 15 months, Serious adverse events and adverse events, Data Safety Monitoring Board (DSMB)

Interventions

Sponsors

Universitaetsmedizin Goettingen
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Disease control rate (DCR) 6 months after treatment start (Complete Response (CR) + Partial Response (PR) + Stable Disease (SD))

Secondary

MeasureTime frame
Disease control rate 3 and 12 months after treatment start, Objective response rate (ORR) 3 months after treatment start and best objective response rate, Progression free survival (PFS) and overall survival (OS), Time on drug (TOD), EORTC QLQ-C30 Quality of Life Questionnaire monthly for 12 months after treatment start and after 15 months, Serious adverse events and adverse events, Data Safety Monitoring Board (DSMB)

Countries

Austria, Germany

Outcome results

None listed

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