Early Phase 1 Prostate Cancer Trial, Recruiting NCT02526368 Sponsor: Ivan de Kouchkovsky, MD Condition: Prostate Cancer
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Early Phase 1 Prostate Cancer Trial, Recruiting

NCT02526368
Recruiting Early Phase 1

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 prostate cancer (a type called adenocarcinoma) confirmed by a tissue sample (biopsy), which may have been done at another hospital as long as detailed results are available.
  • For Group A only: People who are scheduled to have their prostate surgically removed at UCSF within 12 weeks of the study's MRI scans.
  • For Group B only: People who have already completed a targeted prostate treatment called HIFU within the past 18 months, and who are scheduled for a guided biopsy at UCSF within 12 weeks of the study's MRI scans.
  • People who are willing and able to follow study procedures and sign a consent form.
  • People who are generally fit and able to carry out everyday activities with little or no limitation (this is measured by a standard medical scoring system called ECOG, score of 0 or 1).

Who may not be able to join:

  • People under 18 years of age, or those whose general health, mental health, or physical condition means they cannot meaningfully agree to take part in the study.
  • People who are unable to have an MRI scan, including those with certain medical devices such as a pacemaker or certain types of brain clips that are not safe in MRI machines.
  • People who cannot tolerate or have medical reasons to avoid a special internal imaging device used during the MRI scan (called an endorectal coil), such as those who have had certain bowel surgery or who have a latex allergy — though the trial's lead doctor may waive this requirement in some cases.
  • People who cannot receive the contrast dye used during MRI (called gadolinium), for example those with a documented allergy to it or those with poor kidney function.
  • People who have a metal hip implant or any other metal implant or device that could interfere with MRI scan quality.
  • People who have previously had surgery, freezing treatment (cryosurgery), or radiation therapy for prostate or pelvic cancer before joining the study — though for Group B, prior HIFU treatment is allowed; prior prostate scraping surgery (TURP) is not allowed for either group.
  • People who are currently using or have previously used hormone-blocking therapy (androgen deprivation therapy); use of a specific type of prostate medication called a 5-alpha reductase inhibitor may be allowed, provided it was stopped at least one month before joining (Group A) or at least 14 days before the MRI scans (Group B).
  • People with poorly controlled high blood pressure (above 160/100 at the time of joining), though adjusting blood pressure medications to bring it under control may allow eligibility to be re-assessed.
  • People with significant heart failure, classified at a moderate or severe level by a standard medical scale.
  • People with a significant history of abnormal heart electrical readings (ECG), a family history of a specific heart rhythm condition (long QT syndrome), or those who have had a heart attack within the past 6 months — though people with a controlled irregular heart rhythm (atrial fibrillation or flutter) may still be considered.

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 23 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Ivan de Kouchkovsky, MD, University of California, San Francisco

Phone: (415) 502-1822

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
Early Phase 1
Sponsor
Ivan de Kouchkovsky, MD
Registry
ClinicalTrials.gov
Start date
22 March 2016
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Mean peak intra-tumoral lactate/pyruvate (lac/pyr) ratio by pathological grade (Cohort A); Mean peak intra-tumoral lactate/pyruvate (lac/pyr) ratio (Cohort B); Mean lactate area under curve (AUC) by pathological grade (Cohort A); Mean lactate area under curve (AUC) (Cohort B); Mean peak conversion of HP 13C pyruvate to lactate (kPL) by pathological grade (Cohort A); Mean peak conversion of HP 13C pyruvate to lactate (kPL) (Cohort B); Mean Urea AUC by pathological grade (Cohort A); Mean Urea AUC (Cohort B); Mean urea transfer constant (Ktrans) by pathological grade (Cohort A); Mean urea transfe...

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: 23 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