Available in Spain, Chile, Peru, Brazil, United States
Approximately 1800 adult participants with mCSPC will be assigned to one of two cohorts (550
HRRm and 1250 non-HRRm) and randomized in a 1:1 ratio to receive either Saruparib (AZD5305)
with NHA or placebo with NHA. They will receive their assigned treatment and regular tumor
evaluation scans until disease progression, or until treatment is stopped for another reason.
All patients will be followed for survival until the end of the study. Independent data
monitoring committee (DMC) composed of independent experts will be convened to confirm the
safety and tolerability of Saruparib + physicians choice NHA.
1800Patients around the world