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Study of RYZ401 in Subjects With Solid Tumors Expressing SSTRs.
Trial Status: active
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.
Inclusion Criteria
At least 18 years old at the time of signing the main study informed consent form (ICF).
Histologically confirmed: Dose Escalation (all cohorts): Grades 1-3 WD, metastatic or locally advanced and
unresectable NET at any primary site, including, but not limited to, GI, pancreatic,
lung, thyroid, breast, urogenital, and adrenal tumors.
Dose Expansion Cohort A: Grades 1-3 WD, metastatic or locally advanced and unresectable GEP-NETs
Dose Expansion Cohort B: metastatic or locally advanced and unresectable tumors known to frequently express SSTR, limited to the following indications:
WD NETs (Grades 1-3) from primary sites other than gastrointestinal and pancreatic (including, but not limited to, lung, thyroid, breast, urogenital, and adrenal tumors) Meningioma (Grades 1-3)
SSTR-positive disease, as assessed by SSTR-PET imaging
Adequate renal, hematologic and hepatic function
Exclusion Criteria
Prior RPT, including Lu-177.
Prior solid organ or bone marrow transplantation.
Use of chronic systemic steroid therapy.
Significant cardiovascular disease
Resistant hypertension
Uncontrolled diabetes
Prior history of liver cirrhosis
HIV, hepatitis B infection or known active hepatitis C virus infection. Note: Additional criteria may apply and will be assessed by the study site
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07165132.
Locations matching your search criteria
United States
Iowa
Iowa City
University of Iowa/Holden Comprehensive Cancer Center