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This study tests a PARP inhibitor; the registry reports that it is active not recruiting.
The registry lists NCT06421935 as active not recruiting, last updated 2026-09-09. Enrolment is 60 actual participants. Interventions: M9466, Tuvusertib, Abiraterone acetate, Prednisone/Prednisolone. Primary measures include Module 1 Part A1 and Part A2: Number of Participants With Treatment-Emergent Adverse Events (TEAE), and Treatment-related AEs (TRAEs); Module 1 Part A1 and Part A2: Number of Participants with Dose Limiting Toxicity (DLT)-like events. No results are posted in the registry; this does not exclude separate publications.
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