About this trial

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.

Eligibility criteria

Qualifiers

At least 18 years old at the time of signing the main study informed consent form (ICF).

Dose Expansion Cohort A: Grades 1-3 WD, metastatic or locally advanced and unresectable GEP-NETs

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

Disqualifiers

Prior RPT, including Lu-177.

Prior solid organ or bone marrow transplantation.

Use of chronic systemic steroid therapy.

Significant cardiovascular disease

Trial design

Treatments tested in this trial

  • RYZ401

Treatment groups

104 Participants
are divided into 1 treatment group

Locations

9
Canada
Research FacilityM5G 2C4, TorontoOntario, Canada
Research FacilityH3T 1E2, MontrealQuebec, Canada
United States
Iowa
Research Facility52242, Iowa City United States
Kentucky
Research Facility40536, Lexington United States

Sponsors and collaborators

RayzeBio, Inc.

Lead sponsor