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Recruiting NCT05613738

177Lu-PSMA-EB-01 in Patients With Metastatic Castration-resistant Prostate Cancer

Trial Parameters

Condition Metastatic Castration-resistant Prostate Cancer
Sponsor Peking Union Medical College Hospital
Study Type INTERVENTIONAL
Phase N/A
Enrollment 9
Sex MALE
Min Age 18 Years
Max Age 80 Years
Start Date 2022-11-23
Completion 2025-06-30
Interventions
1.11 GBq (30 mCi) of 177Lu-PSMA-EB-011.85 GBq (50 mCi) of 177Lu-PSMA-EB-012.59 GBq (70 mCi) of 177Lu-PSMA-EB-01

Brief Summary

This is a pilot study to assess the safety and measure image-based absorbed dose of 177Lu-PSMA-EB-01, a new PSMA-specific radiopharmaceutical, in patients with metastatic castration resistant prostate cancer (mCRPC) who will undergo radioligand therapy (RLT). All patients underwent 68Ga-PSMA and 18F-FDG PET/CT for selection and were randomly divided into three groups of 3 people each.The three groups received an approximately 1.11 GBq (30mCi), 1.85 GBq (50 mCi) and 2.59 GBq (70mCi) of 177Lu-PSMA-EB-01 up to 2 cycles, respectively.

Eligibility Criteria

Inclusion Criteria: * progressive metastatic castration-resistant prostate cancer * tumors with high PSMA expression confirmed on 68Ga-PSMA PET/CT Exclusion Criteria: * a serum creatinine level of more than 150 μmol per liter * a hemoglobin level of less than 10.0 g/dl * a white-cell count of less than 4.0× 109/L * a platelet count of less than 100 × 109/L * a total bilirubin level of more than 3 times the upper limit of the normal range * a serum albumin level of more than 3.0 g per deciliter * cardiac insufficiency

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