A Phase 2 Open-label Study Evaluating Dosimetry Randomized Dose Optimization Dose Escalation and Efficacy of Ac-225 Rosopatamab Tetraxetan in Participants with PSMA PET-Positive Castration-Resistant Prostate Cancer
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Prostate CancerProstate
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Age: Between 18 Year(s) - 99 Year(s)
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Gender: Male
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Other Inclusion Criteria:
- Serum PSA progression consisting of two consecutive increases in PSA measured at least 1 week apart. The minimal baseline value is 2.0 ng/mL.
- Progression of bone disease defined by PCWG3 as evaluable disease or new bone lesions by bone scan.
- Identification of new soft tissue or bone lesions on PSM
You may not be eligible for this study if the following are true:
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- Superscans by nuclear medicine/99mTc bone scan
- A known malignancy that is progressing or has required active treatment within the past 3 years other than CRPC, which is expected to alter life expectancy or may interfere with CRPC disease assessment.
- Known active uncontrolled or symptomatic central nervous system (CNS) metastases and/or progressive carcinomatous meningitis, or progressive leptomeningeal disease as indicated by clinical symptoms, cerebral edema, and/or progressive growth.
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.