Status:
RECRUITING
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 (CRPC)
Lead Sponsor:
Convergent Therapeutics
Conditions:
PSMA PET-Positive Castration-Resistant Prostate Cancer
Eligibility:
MALE
18+ years
Phase:
PHASE2
Brief Summary
This is a three-part study evaluating the safety and efficacy of a PSMA-directed radioantibody (rosopatamab tetraxetan, conjugated to either In-111 or Ac-225). Part 1 will consist of one administratio...
Eligibility Criteria
Inclusion
- Progressive CRPC defined as castrate levels of testosterone and progressing by at least one of the following criteria:
- Serum PSA progression consisting of two consecutive increases in PSA measured at least 1 week apart. The minimal study baseline value is 2.0 ng/mL
- Soft tissue progression defined as a ≥20% increase in the sum of the diameter (short axis for nodal lesions and long axis for non-nodal lesions) of all target lesions based on the smallest sum of the diameter since the previous treatment was started or the appearance of one or more new lesions by CT/magnetic resonance imaging (MRI)
- 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 PSMA PET imaging
- Metastatic disease defined as either or both of the following:
- Parts 1, 2 and 3: Documented M1 disease on conventional imaging (CT/MRI of the chest/abdomen/pelvis and/or Technetium 99m \[99mTc\] whole-body bone scan)
- Parts 1 and 2 only: Identification of bone lesion(s), extra-pelvic soft tissue lesion(s), or visceral metastases on PSMA PET imaging with an FDA-approved imaging agent
- PSMA PET-positive disease, defined as at least one PSMA-positive metastatic lesion and no PSMA-negative lesions
- Progression following treatment with ADT and at least one ARSI (e.g., enzalutamide, apalutamide, darolutamide, and/or abiraterone acetate)
- The standard of care use (in the setting of metastatic CRPC with significant burden of active bone metastases) of antiresorptive bone-targeted agents (e.g., zoledronic acid, denosumab) is required for all participants without a contraindication, for at least 4 weeks prior to study drug administration
- Participants with HIV are eligible if they are well-controlled (i.e, an undetectable HIV viral load (\<50 copies/mL) within 6 months of enrollment and a stable ART regimen for at least 6 months prior to enrollment) and at low risk for HIV-related illness
- Part 3 Only:
- Prior treatment with Lu-177-PSMA-radioligand therapy
- Prior treatment with up to only one taxane-based chemotherapy regimen is allowed
Exclusion
- 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
- Prior platinum-based chemotherapy
- Prior PARP inhibitors (e.g., olaparib or rucaparib)
- Prior treatment with Radium-223, Actinium-225, Strontium-89, Samarium-153, Rheunium-186, or Rhenium-188
- Participants receiving anti-coagulants or anti-platelet drugs (e.g., aspirin or nonsteroidal anti-inflammatory drugs \[NSAIDs\]) who cannot discontinue use if platelet count decreases to \<50,000
- Part 2 Only:
- Prior chemotherapy for CRPC. Prior taxane chemotherapy for HSPC is allowed if discontinued ≥1 year prior to randomization
- Prior radiopharmaceutical therapy (e.g., Ra-223, Lu-177-PSMA-617, or Lu-177-PSMA-I\&T)
- Prior PSMA-targeted therapy
- Part 3 Only:
- Prior PSMA-targeted therapy (e.g., antibody-drug conjugates or CAR-T therapy), except for Lu-177-PSMA-radioligand therapy
Key Trial Info
Start Date :
August 6 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2027
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06549465
Start Date
August 6 2024
End Date
April 1 2027
Last Update
August 24 2025
Active Locations (9)
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1
University of California San Diego
San Diego, California, United States, 92093
2
Dana-Farber Cancer Institute
Boston, Massachusetts, United States, 02215
3
Washington University in St. Louis
St Louis, Missouri, United States, 63130
4
X Cancer Omaha / Urology Cancer Center
Omaha, Nebraska, United States, 68130-5606