Phase 2 Prostate Cancer Trial, Recruiting
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 have been diagnosed with a specific type of prostate cancer (adenocarcinoma or poorly differentiated carcinoma) confirmed by laboratory testing of tissue — note that cancers made up entirely of small-cell or high-grade neuroendocrine cells are not eligible, though some neuroendocrine features are allowed.
- People whose testosterone levels have been reduced to very low levels (≤ 50 ng/dL) either through surgery to remove the testicles or through ongoing hormone-blocking medication, which must be continued throughout the study.
- People whose cancer has continued to grow or spread despite previous treatment, shown by at least one of: two rising PSA blood test results taken at least one week apart (with the most recent being ≥ 2 ng/mL), new or growing tumours visible on a CT or MRI scan, or at least two new areas of cancer detected on a bone scan.
- People who have signed an informed consent form before any study-related procedures begin.
- People aged 18 years or older.
- People with a life expectancy of at least 3 months.
- People with a good general health and activity level, rated 0 or 1 on a standard performance scale (confirm with trial site).
- People whose blood, liver, and kidney function results fall within the ranges required by the trial (confirm with trial site for specific values).
Who may not be able to join:
- People who have had significant surgery to remove part of the stomach or small intestine, or who have a condition that affects the body's ability to absorb food or medication taken by mouth.
- People with serious ongoing physical or mental health conditions that the trial doctor considers incompatible with participation.
- People with an active infection at the time of joining, as assessed by the trial doctor.
- People with conditions affecting the brain or nervous system — including epilepsy or significant confusion — that would prevent them from understanding the consent process or completing study procedures.
- People currently taking a specific class of medications known as cationic amphiphilic drugs, including some that are available without a prescription (confirm with trial site for the full list).
- People currently taking another experimental drug as part of a different trial or study.
- People who have had an allergic reaction to any of the medications used in this trial.
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.
Contact this trial
Principal Investigator: Helle Pappot, DMsc, Rigshospitalet, Denmark
Phone: +4535458403
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
Where this trial is recruiting
Primary endpoints
Changes in the profile and concentration of urinary lipids and blood lipids
Can't join this trial?
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.