Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT04015622 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.
This record was last updated August 20, 2025 (before its estimated April 1, 2026 completion). Its status may not reflect the trial's current state.
Record History
NotablePrimary completion date: Apr 1, 2025 to Apr 1, 2026Trial status: Recruiting to Active, Not Recruiting · Completion date: Dec 1, 2025 to Dec 1, 2026 · Site details revised at 7 of 7 sitesv18Show 3 more changesShow less
Trial status: Recruiting to Active, Not Recruiting
Completion date: Dec 1, 2025 to Dec 1, 2026
Site details revised at 7 of 7 sites
MinorStudy sites: 6 to 7v17
MinorSite details revised at 2 of 6 sitesv16
MinorStudy sites: 5 to 6v15
MinorStudy sites: 4 to 5v14
Show 12 earlier versionsHide 12 earlier versions
NotablePrimary completion date: Dec 1, 2023 to Apr 1, 2025Completion date: Dec 1, 2024 to Dec 1, 2025v13Show 1 more changeShow less
Completion date: Dec 1, 2024 to Dec 1, 2025
Minor2 versionsRe-verified since Jul 11, 2022, no change to tracked fieldsv11-v12
NotableTrial status: Active, Not Recruiting to RecruitingSite details revised at 5 of 5 sitesv4Show 1 more changeShow less
Site details revised at 5 of 5 sites
MinorTrial status: Not Yet Recruiting to Active, Not RecruitingSite contacts updated at 5 of 5 sitesv3Show 1 more changeShow less
Site contacts updated at 5 of 5 sites
NotablePrimary completion date: Dec 1, 2021 to Dec 1, 2023Start date: Dec 1, 2019 to Oct 7, 2020 · Study sites: 0 to 5 · Completion date: Dec 1, 2022 to Dec 1, 2024 · 3 morev2Show 6 more changesShow less
Stopped: an ongoing trial was terminated, suspended or withdrawn.
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 purpose of this study is to assess the strategy in treatment selection using ctDNA fraction as a predictive biomarker to direct treatment decision (ctDNA fraction \<2% receives enzalutamide, and ctDNA fraction ≥2% receives docetaxel) versus clinician's choice of enzalutamide or docetaxel, in subjects with metastatic castration-resistant prostate cancer post abiraterone setting.