Prostate Cancer Trial, Recruiting NCT07093801 Sponsor: Novartis Pharmaceuticals Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT07093801
Recruiting Not Applicable

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:

  • Adults who have been diagnosed with metastatic castration-resistant prostate cancer (a type of prostate cancer that has spread and no longer responds to hormone treatment) and whose treating medical team has assessed them as suitable and prescribed a specific treatment called lutetium (177Lu) vipivotide tetraxetan.
  • People who are 18 years of age or older at the time of joining the study.
  • People who are willing and able to provide written consent to take part in the study.

Who may not be able to join:

  • People for whom lutetium (177Lu) vipivotide tetraxetan is considered medically unsuitable, based on the official prescribing guidelines for this treatment (confirm with trial site).
  • People who do not meet the additional requirements set out in the official Italian medicines regulatory documentation (the AIFA Monitoring Form), which may include specific medical contraindications (confirm with trial site).

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
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

Principal Investigator: Novartis Pharmaceuticals, Novartis Pharmaceuticals

Phone: +41613241111

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
Registry
ClinicalTrials.gov
Start date
30 July 2025
Est. completion
30 March 2029

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Progression-Free Survival (PFS)

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