The primary objectives are to determine the recommended Phase 2 dose (RP2D) and optimal treatment regimen, characterize safety and tolerability, and evaluate preliminary efficacy of RYZ401 in subjects with NETs and other selected solid tumors expressing SSTRs.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
104
Ac-225
Research Facility
Iowa City, Iowa, United States
RECRUITINGResearch Facility
Lexington, Kentucky, United States
RECRUITINGResearch Facility
St Louis, Missouri, United States
RECRUITINGResearch Facility
Salt Lake City, Utah, United States
RECRUITINGDose Escalation
Incidence of DLTs during RYZ 401 Treatment
Time frame: Incidence of DLTs during the first 4 weeks of RYZ401 treatment
Dose Expansion
Incidence, severity, and duration of AEs
Time frame: Cycle1 Day 1 to LPFV + 6 weeks
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