The primary objective of this study is to measure efficacy of saruparib + physician's choice of ARPI compared with placebo + ARPI in men with metastatic hormone-sensitive prostate cancer (mHSPC) who have previously received docetaxel chemotherapy or a prostate-specific membrane antigen (PSMA)-directed lutetium-177 radioligand therapy with no evidence of disease progression and PSA ≥ 0.2 ng/mL.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
1,330
Arm 1: Saruparib (AZD5305) + Physician's Choice ARPI (enzalutamide, darolutamide, or abiraterone)
Arm 2: Placebo + Physician's Choice ARPI (enzalutamide, darolutamide, or abiraterone)
Arm 1: Saruparib (AZD5305) + Physician's Choice ARPI (enzalutamide, darolutamide, or abiraterone) Arm 2: Placebo + Physician's Choice ARPI
Arm 1: Saruparib (AZD5305) + Physician's Choice ARPI (enzalutamide, darolutamide, or abiraterone) Arm 2: Placebo + Physician's Choice ARPI
Arm 1: Saruparib (AZD5305) + Physician's Choice ARPI (enzalutamide, darolutamide, or abiraterone) Arm 2: Placebo + Physician's Choice ARPI
Research Site
Ottawa, Ontario, Canada
Research Site
Montreal, Quebec, Canada
Radiographic progression-free survival (rPFS)
Radiographic PFS (rPFS) is the primary endpoint of this study, defined as the time from randomization to radiographic progression, as assessed by the investigator per RECIST 1.1 (soft tissue) and/or PCWG3 criteria (bone), or death due to any cause.
Time frame: Up to approximately 56 months
Overall Survival (OS)
OS is defined as the time from the date of randomization until death due to any cause.
Time frame: Up to approximately 80 months
Radiographic progression-free survival (rPFS)
Radiographic PFS (rPFS) is the primary endpoint of this study, defined as the time from randomization to radiographic progression, as assessed by the investigator per RECIST 1.1 (soft tissue) and/or PCWG3 criteria (bone), or death due to any cause.
Time frame: Up to approximately 56 months
Time to Second Progression or Death (PFS2)
PFS2 is defined as the time from randomization to the earliest progression (defined as radiographic progression, clinical progression, or PSA progression) after initiation of first subsequent treatment following the initial investigator-assessed progression or death (ie, date of PFS2 event or censoring - date of randomization + 1).
Time frame: Up to approximately 56 months
Time to First Subsequent Therapy or Death (TFST)
TFST is defined as the time from randomization to the start date of the first subsequent anticancer therapy after discontinuation of randomized treatment, or death due to any cause (ie, date of first subsequent cancer therapy or death - date of randomization + 1).
Time frame: Up to approximately 56 months
Symptomatic Skeletal Event-free Survival (SSE-FS)
SSE-FS is defined as the time from the date of randomization to the earliest of the following: * Use of radiation therapy to prevent or relieve skeletal symptoms. * Occurrence of new symptomatic pathological bone fractures (vertebral or non-vertebral). Radiographic documentation is required. A pathological fracture, as determined by investigator, is defined as associated with low or no trauma and deemed to have occurred at a site of bone metastasis. * Occurrence of spinal cord compression. Radiographic documentation is required. * Orthopedic surgical intervention for bone metastasis. * Death due to any cause.
Time frame: Up to approximately 56 months
Time to Castration Resistance (TTCR)
TTCR is defined as the time from randomization to the first castration-resistant event (radiographic disease progression, PSA progression per PCWG3, or SSE, whichever occurs first, with castrate levels of testosterone below 50 ng/dL).
Time frame: Up to approximately 56 months
Time to PSA progression
Time to PSA progression, defined as the time from randomization to PSA progression per PCWG3 criteria.
Time frame: Up to approximately 56 months
Time to deterioration in physical function (TTDPF)
TTDPF is defined as the time from randomization to deterioration in PROMIS SF-PF scores.
Time frame: Up to approximately 56 months
Time to pain progression (TTPP)
TTPP is defined as the time from randomization to clinically meaningful pain progression based on a 2-point increase from baseline in the BPI-SF Item 3 'worst pain in 24 hours' score and/or initiation of/increase in opioid analgesic use.
Time frame: Up to approximately 56 months
Brief Pain Inventory - Short Form (BPI-SF)
Change from baseline in BPI-SF worst pain score, pain severity and interference domain scores.
Time frame: Up to approximately 56 months
Time to deterioration in urinary symptoms (TTDUS)
TTDUS is defined as the time from randomization to deterioration in the EORTC QLQ-PR25(US) subscale scores.
Time frame: Up to approximately 56 months
Plasma concentrations of AZD5305
To assess PK of AZD5305 in plasma
Time frame: Day 1 of Cycle 1, Cycle 2 and Cycle 3 (each cycle is of 28 days)
AstraZeneca Clinical Study Information Center
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