Phase 3 Prostate Cancer Trial, Recruiting NCT07028853 Sponsor: Pfizer Condition: Prostate Cancer
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Phase 3 Prostate Cancer Trial, Recruiting

NCT07028853
Recruiting Phase 3 🇦🇺 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:

  • Male participants who are 18 years of age or older at the time of screening (or the minimum age required by local rules).
  • People whose prostate cancer has been confirmed by a tissue or cell sample as adenocarcinoma (a specific type of prostate cancer), without certain aggressive small cell features.
  • People whose prostate cancer has spread to other parts of the body, confirmed by a bone scan, CT scan, or MRI.
  • People whose side effects from any previous treatment have largely settled down to a mild level or back to how they were before treatment started.
  • People who are generally well enough to carry out daily activities with little or no limitation (this is measured using a standard medical scale — confirm with trial site).

Who may not be able to join:

  • People with certain medical or psychiatric conditions, including thoughts of suicide or self-harm within the past year or currently, or certain abnormal lab results that the doctor feels make participation unsafe.
  • People with serious heart or blood vessel disease.
  • People with cancer that has spread to the brain, or with a related condition affecting the lining of the brain or spinal cord.
  • People who have already received certain cancer treatments (such as chemotherapy) for their metastatic prostate cancer — though treatment with a specific older type of hormone therapy (first-generation antiandrogen/ADT) is an exception and may be allowed (confirm with trial site).
  • People who have taken part in another clinical trial involving an experimental drug or vaccine within the past 30 days.
  • People who have used a type of medication called 5-alpha reductase inhibitors within 28 days before joining the trial.
  • People who have had surgery recently and have not fully recovered at least 28 days before joining the trial.
  • People currently taking or expecting to need certain medications that strongly affect how the body processes drugs (known as strong CYP3A4/5 inhibitors or inducers) — with one exception that may apply within this trial (confirm with trial site).
  • People whose kidneys, liver, or other organs are not functioning well enough (confirm with trial site).
  • People with a known allergy or sensitivity to the study drugs (mevrometostat or enzalutamide) or any of their ingredients.

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 7 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

Australian sites

Orange Health Service, Orange, New South Wales
Sydney Adventist Hospital, Wahroonga, New South Wales
Icon Cancer Centre Chermside, Chermside, Queensland
Mater Misericordiae Limited Mater Cancer Care Centre, South Brisbane, Queensland
ICON Cancer Centre - Kurralta Park, Kurralta Park, South Australia
Sir Charles Gairdner Hospital, Nedlands, Western Australia

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
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
28 September 2025
Est. completion
12 September 2028

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇪 Belgium 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇦 Canada 🇨🇳 China 🇨🇿 Czechia 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇿 New Zealand 🇵🇱 Poland 🇸🇰 Slovakia 🇰🇷 South Korea 🇪🇸 Spain 🇨🇭 Switzerland 🇹🇼 Taiwan Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Radiographic Progression Free Survival (rPFS)

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: 7 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