ClinicalTrials.gov record
Recruiting Phase 2 Interventional

Abiraterone and Prednisone or Darolutamide for the Treatment of Advanced Prostate Cancer

ClinicalTrials.gov ID: NCT06173362

Public ClinicalTrials.gov record NCT06173362. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 29, 2026, 8:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pragmatic Phase II Study Evaluating Tolerability in Prostate Cancer Patients Treated With Abiraterone + Prednisone or Darolutamide

Study identification

NCT ID
NCT06173362
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
University of California, Davis
Other
Enrollment
75 participants

Conditions and interventions

Interventions

  • Abiraterone Drug
  • Biospecimen Collection Procedure
  • Darolutamide Drug
  • Prednisone Drug

Drug · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 8, 2023
Primary completion
Oct 31, 2026
Completion
Apr 30, 2027
Last update posted
Mar 12, 2026

2023 – 2027

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University of California Davis Comprehensive Cancer Center Sacramento California 95817 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06173362, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 12, 2026 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06173362 live on ClinicalTrials.gov.

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