A Study of Xaluritamig Plus Abiraterone Versus Investigator's Choice in Participants With Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer
Secondary endpoints: details revised at 2 of 36 entries
MinorTrial sites expanded: 151 → 155 locationsv26
MinorStudy sites: 150 to 151v25
MinorStudy sites: 149 to 150v24
MinorTrial sites expanded: 144 → 149 locationsv23
MinorTrial sites expanded: 140 → 144 locationsv22
MinorTrial sites expanded: 136 → 140 locationsv21
MinorSite details revised at 1 of 136 sitesv20
MinorStudy sites: 134 to 136v19
MinorStudy sites: 133 to 134v18
MinorTrial sites expanded: 129 → 133 locationsv17
MinorStudy sites: 127 to 129v16
MinorStudy sites: 126 to 127v15
MinorStudy sites: 125 to 126v14
MinorTrial sites expanded: 122 → 125 locationsv13
MinorStudy sites: 120 to 122v12
MinorTrial sites expanded: 117 → 120 locationsv11
MinorStudy sites: 116 to 117v10
MinorTrial sites expanded: 94 → 116 locationsv9
MinorStudy sites: 90 to 94v8
MinorStudy sites: 79 to 90v7
MinorStudy sites: 60 to 79v6
MinorStudy sites: 31 to 60
Eligibility criteria expanded, about 3 words
v5
NotablePrimary completion date: Aug 29, 2028 to Jan 7, 2030
Study sites: 26 to 31
Secondary endpoints: details revised at 36 of 36 entries
v4
MinorStudy sites: 4 to 26
Start date changed from estimate of Nov 1, 2025 to Nov 28, 2025
v3
NotableTrial status: Not Yet Recruiting to Recruiting
Study sites: 0 to 4
v2
Study First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary objective of this study is to compare overall survival (OS) in participants receiving xaluritamig plus abiraterone against investigator's choice (docetaxel, cabazitaxel, or abiraterone).