Phase 1 Prostate Cancer Trial, Recruiting NCT07493512 Sponsor: Amgen Condition: Prostate Cancer
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Phase 1 Prostate Cancer Trial, Recruiting

NCT07493512
Recruiting 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 confirmed through laboratory testing (tissue or cell samples) to have prostate adenocarcinoma (a specific type of prostate cancer), but not a mixed type that includes a neuroendocrine component.
  • People who have prostate cancer that has spread to other parts of the body (metastatic) and is no longer responding to hormone therapy (castration-resistant), with at least one visible spread shown on a scan taken within 28 days before joining.
  • People whose cancer has been getting worse, shown by rising PSA blood test levels, growth of tumours in soft tissue, or the appearance of new spots on bone scans, according to specific medical guidelines (confirm with trial site).
  • People who have had surgical removal of the testicles or are receiving ongoing hormone-suppression therapy, with testosterone levels confirmed to be at a very low (castrate) level.
  • People whose cancer has previously gotten worse during or after treatment with at least one specific type of hormone-blocking drug (such as enzalutamide, abiraterone, apalutamide, or darolutamide).
  • People who have received one, and only one, taxane chemotherapy treatment while their cancer was in the castration-resistant stage (a prior taxane given during an earlier hormone-sensitive stage is also allowed, but only if exactly one taxane was also given in the later stage).

Who may not be able to join:

  • People who have a history of cancer spreading to the brain or spinal cord, unless the spread was to the lining of the brain only, has been treated, is causing no symptoms, and is considered stable (confirm with trial site).
  • People who have had a serious allergic or hypersensitivity reaction to any of the trial medications or similar drugs, or who have a medical reason they cannot take high-dose steroids.
  • People who have or have had another cancer that could affect life expectancy or make it harder to assess the prostate cancer, unless that other cancer was fully treated and has been in remission for more than 3 years, or was a type of non-melanoma skin cancer or a surface-level bladder cancer that was adequately treated.
  • People who have an active autoimmune disease that has needed systemic (whole-body) treatment within the past 2 years, or any condition that would require immune-suppressing medication during the trial.
  • People who have tested positive for HIV.
  • People who have a current or past viral hepatitis infection.
  • People who have received anti-cancer treatments (such as chemotherapy, targeted therapy, hormonal therapy, or another trial drug) within 28 days before the first trial dose, with some specific exceptions around certain hormone therapies and timing rules (confirm with trial site).
  • People who have previously received any therapy that targets a protein called STEAP1.
  • People who have previously received any therapy that targets a protein called CD3.
  • People who need ongoing daily steroid medication above a low dose threshold, or any other ongoing immune-suppressing treatment.
  • People who have taken part in any other clinical trial involving the study drug xaluritamig, even if they did not actually receive that drug.

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
Phase 1: approximately ~10% 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: MD, Amgen

Phone: 866-572-6436

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 1
Sponsor
Registry
ClinicalTrials.gov
Start date
28 April 2026
Est. completion
30 January 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Participants with Treatment-emergent Adverse Events

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