Overview

Study of Cabozantinib With Lu-177 in Patients With Somatostatin Receptor 2 Positive Neuroendocrine Tumors

Status:
Not yet recruiting
Trial end date:
2031-12-01
Target enrollment:
Participant gender:
Summary
The phase I objective of this study is to establish the maximal tolerated dose (MTD) of cabozantinib in 20 mg, 40 mg and 60 mg dose escalation cohorts in combination with Lu-177 dotatate at a standard dose of 7.4 GBq in four (4) 8-week cycles followed by continuation cabozantinib.
Phase:
Phase 1
Details
Lead Sponsor:
Providence Health & Services
Collaborators:
Advanced Accelerator Applications SA
Exelixis
Treatments:
Lutetium Lu 177 dotatate