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Clinical Trial · NCT06200558
Overview
Study wants to explore real-world data in three distinct settings * Patients with metachronous or de novo mCSPC treated with ADT+ARSI or ADT+ARSI+docetaxel \_ARON-3S * Patients receiving Lutetium-177 PSMA for mCRPC \_ ARON-3Lu * Patients treated with PARP inhibitors (alone or combined with ARSI) for CRPC \_ ARON-3GEN
Sponsor
Xiangya Hospital of Central South University
Contacts
Matteo Santoni (CONTACT)
sorgentoni.giulia@gmail.com
+39 07332573752
ClinicalTrials.gov
NCT06200558Drug / Compound
Eligibility
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