About this trial

This imaging study aims to assess the feasibility, biodistribution, and dosimetry of a TROP2 binder in subjects with metastatic UC, HR+ and HER2- breast cancer, TNBC, or NSCLC.

Eligibility criteria

Qualifiers

Are at least 18 years old at the time of signing the informed consent form (ICF)

Have biopsy proven metastatic UC, HR+ and HER2- breast cancer, TNBC, or NSCLC

Disqualifiers

TROP2-targeting antibody-drug conjugates (ADCs) such as sacituzumab govitecan or datopotamab deruxtecan, should be discontinued at least 90 days prior to administration of RYZ211 and RYZ212

For Women of Childbearing Potential: Are pregnant or breastfeeding

Trial design

Treatments tested in this trial

  • RYZ211/212

Treatment groups

40 Participants
are divided into 1 treatment group

Locations

1
Research Facility Christchurch New Zealand

Sponsors and collaborators

RayzeBio, Inc.

Lead sponsor