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This prospective study aims to collect data and blood biomarkers from patients undergoing Lu-PSMA therapy at the Erasmus MC. In doing so, it will provide real-world efficacy and safety data on the drug, gather dosimetry data and explore putative biomarkers to identify patients who most benefit from Lu-PSMA treatment.
Age
18 - No limit years
Sex
MALE
Healthy Volunteers
No
Erasmus MC
Rotterdam, South Holland, Netherlands
Start Date
February 20, 2024
Primary Completion Date
February 1, 2027
Completion Date
February 1, 2027
Last Updated
April 22, 2024
150
ESTIMATED participants
Blood draw for ctDNA and circulating tumor cell collection.
DIAGNOSTIC_TEST
Lead Sponsor
Erasmus Medical Center
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06242119