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Targeted a-Therapy in Prostate Cancer

Targeted a-Therapy in Metastatic Castration Resistant Prostate Cancer with 225Ac-PSMA-617

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210612051548N1
Enrollment
10
Registered
2021-09-22
Start date
2021-11-22
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate cancer. Malignant neoplasm of prostate

Interventions

Intervention group: In this study, the 225Ac-PSMA-617 radiopharmaceutical is injected intravenously into 10 patients with prostate cancers according to the 68Ga-PSMA-11 PET/CT. Then whole-body scan is

Sponsors

Boushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients must have had progressive metastatic castration-resistant prostate cancer. Patients must have a positive 68Ga-PSMA-11 PET/CT scan. Patients must have recovered or stabilized to = Grade 2 from all clinically significant toxicities related to prior prostate cancer therapy. Patients must have an ECOG performance status of 0 to 2.

Exclusion criteria

Exclusion criteria: Previous treatment with Strontium-89, Samarium-153, Rhenium-186, Rhenium-188, Radium-223 or hemi-body irradiation or previous PSMA-targeted radioligand therapy. The patient was diagnosed with other malignancies that are expected to alter life expectancy or may interfere with disease assessment (Patients with a prior history of malignancy who have been disease-free for more than 3 years are eligible).

Design outcomes

Primary

MeasureTime frame
Numbe of treated prostate cancer patients. Timepoint: 4-6 weeks after last treatment session. Method of measurement: Image-based response using 68Ga-PSMA PET/CT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Assadi

Boushehr University of Medical Sciences

assadipoya@yahoo.com+98 77 3332 0361

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026