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Mechanisms of Resistance to PSMA Radioligand Therapy
RecruitingObservational study
Mechanisms of Resistance to PSMA Radioligand Therapy: Radiation Resistance Versus Dose
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: 1. Initiating treatment with Lutetium based PSMA-targeted RLT. 2. Participants must have a PSMA-avid lesion that is accessible to biopsy. Biopsy of newly emerging radiographic metastases is desired and preferable to the biopsy of previously existing lesions whenever possible. Newly emerging lesions are defined as those that are absent on a previous scan, or those demonstrating unequivocal progression since initiation of the last treatment. Biopsies will be performed according to local institutional standards. 3. Patients on warfarin, aspirin, or other anti-coagulants are eligible provided they are deemed able to tolerate discontinuation of anti-coagulation for at least five days prior to the biopsy. Conversion to low molecular weight heparin prior to biopsy is permitted per local standard operating procedures, provided there is approval by the interventional radiologist or the PI. 4. Age \>=18 years. 5. Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria: 1. Patients with significant congenital or acquired bleeding disorders (eg von Wildebrand's disease, acquired bleeding factor inhibitors). 2. Patients who are not able to undergo additional study related imaging procedures.
About the study
This is a multicenter, correlative study to existing Lutetium based prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) trials and uses.
What is being tested
- Single-photon emission computed tomography (procedure)
- Blood Draw (procedure)
- Tumor Biopsy (procedure)
Sponsor: University of California, San Francisco · Participants: 125 · Started: Oct 21, 2021
Contact the study team
- Maya Aslam · Phone: (415) 514-8987
Official record on ClinicalTrials.gov — NCT05435495
Locations in the U.S.
| California | University of California, Los Angeles, Los Angeles University of California, San Francisco, San Francisco |
| New York | Memorial Sloan Kettering, New York |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.