The purpose of this study is to learn if the study drug, [225Ac]Ac-PSMA-R2, is safe and
tolerable, and has anti-tumor activity in treated patients.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05983198.
Locations matching your search criteria
United States
Minnesota
Rochester
Mayo Clinic in RochesterStatus: Temporarily closed to accrual
Name Not Available
First in human (FIH) phase I/II study of 225Ac-PSMA-R2 in PSMA-positive metastatic
prostate cancer across three groups: post-177Lu mCRPC, pre-177Lu mCRPC, and 177Lu-naïve
mHSPC, evaluating Q6W/Q4W dosing. Dose escalation will enroll ~18-22 participants per
group/schedule to define MTD/RDE, guided by safety, tolerability, PK/dosimetry, and
preliminary anti-tumor activity, with possible expansion based on benefit-risk.
Enrollment and dosing for all participants in Group 1, Group 2, and Group 3 have been
completed. Further enrollment has been halted, and no additional dose escalation cohorts
or Phase 2 dose expansion cohorts will be opened; enrollment in this study is now
considered complete. The decision to halt enrolment was not driven by any safety concerns
identified in the study to date, but rather by a lowered expectation of benefit.
Accordingly, the study will not proceed to Phase 2, and a recommended Phase 2 dose was
not established
Lead OrganizationNovartis Pharmaceuticals Corporation