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Clinical Trial Summary

The purpose of this program is to provide access to [Lu-177]-PNT2002 to patients who have been diagnosed with prostate-specific membrane antigen (PMSA)-positive castration-resistant prostate cancer (mCRPC). Patients must have received at least 1 prior androgen pathway inhibitor (ARPI) and cannot be treated by currently available drugs or clinical trials. In this program participants will be administered [Lu-177]-PNT2002 intravenously every 8 weeks (about every 2 months) for 4 cycles, or 8 months of total treatment. During treatment, participants will be monitored with routine laboratory tests such as: - Hematology blood tests - Clinical Chemistry blood tests - Testosterone/Prostate Antigen levels blood test - Vital signs - Imaging - ECG


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06033001
Study type Expanded Access
Source Lantheus Medical Imaging
Contact Associate Director Radioligand Clinical Applications
Phone 901-283-5950
Email LNTH-PNT2002-EAP-INFO@lantheus.com
Status Available
Phase

See also
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