Prostate Cancer Trial, Recruiting NCT07223372 Sponsor: Bayer Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT07223372
Recruiting Not Applicable 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are male and have been diagnosed with prostate cancer that has spread to other parts of the body, and whose cancer still responds to hormone treatment (known as metastatic hormone-sensitive prostate cancer)
  • People who have been dispensed at least one of the following medications for the first time during the study period, specifically for this type of prostate cancer: darolutamide, enzalutamide, apalutamide, or abiraterone acetate/methylprednisolone
  • People who were 18 years of age or older at the time their records entered the study
  • People whose medical records include at least 12 months of data before the point they entered the study
  • People whose medical records include at least 3 months of data after the point they entered the study

Who may not be able to join:

  • People who have records showing use of any of the listed medications (darolutamide, enzalutamide, apalutamide, or abiraterone/methylprednisolone) before the point they entered the study
  • People whose records show evidence of prostate cancer that has stopped responding to hormone treatment (castration-resistant prostate cancer), whether or not it has spread, at or before the point they entered the study (confirm with trial site on how this is determined from medication records)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: (+)1-888-84 22937

Australian sites

Bayer, Pymble, New South Wales

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
10 October 2025
Est. completion
30 November 2026

Where this trial is recruiting

🇦🇺 Australia

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Number and proportion of patients taking each ARPI as a percentage of total study population.; Demographic characteristics of mHSPC patients

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov