Phase 1 Prostate Cancer Trial, Recruiting NCT07006727 Sponsor: Novartis Pharmaceuticals Condition: Prostate Cancer
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Phase 1 Prostate Cancer Trial, Recruiting

NCT07006727
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:

  • Adults aged 18 or older
  • People with small cell lung cancer (SCLC) that has spread or cannot be surgically removed, where the cancer has continued to grow or worsened after at least one previous treatment (including a platinum-based chemotherapy, unless that type of treatment was not suitable for them) — previous DLL3-targeted therapy is also permitted
  • People in the dose-finding stage of the trial with a type of lung cancer called large cell neuroendocrine carcinoma (LCNEC), where the cancer has progressed or was not tolerated after at least one previous treatment including platinum-based chemotherapy (unless that treatment was not suitable for them)
  • People in the expansion stage of the trial with a specific type of prostate cancer that has neuroendocrine features (NEPC), confirmed by laboratory testing, who have at least one measurable tumour that shows uptake of a special imaging agent on a specific type of scan (SPECT/CT) as assessed by the investigator — prior PSMA-targeted or lutetium-177-based treatments are permitted
  • People in the expansion stage of the trial with a cancer of the gut or pancreas with neuroendocrine features (GEP-NEC) that has spread or cannot be removed surgically, where the cancer progressed after at least one prior treatment including platinum-based chemotherapy (unless not suitable), and who have at least one measurable tumour showing uptake on the specific imaging scan as assessed by the investigator
  • People joining the expansion stage of the trial should have received no more than two prior lines of treatment overall

Who may not be able to join:

  • People whose blood counts are too low — specifically, low white blood cell levels, low haemoglobin (a measure of red blood cells), or low platelet levels
  • People with a specific type of irregular heart rhythm measurement (a prolonged QTcF interval of 470 milliseconds or more) on a heart tracing (ECG)
  • People whose kidneys are not working well enough, based on a specific calculation of kidney function (confirm with trial site)
  • People with bladder or urinary tract blockages that cannot be managed, or with urinary incontinence that cannot be controlled
  • People who have cancer that has spread to the lining around the brain or spinal cord, or who have brain metastases causing symptoms or requiring local treatment
  • People with a history of, or current, significant lung inflammation or scarring (interstitial lung disease or pneumonitis of Grade 2 or higher)
  • People who have previously received DLL3-targeted therapy (unless they have SCLC) or prior radioligand therapy (unless they have NEPC)

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 22 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

Phone: 1-888-669-6682

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

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Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
16 October 2025
Est. completion
29 August 2031

Where this trial is recruiting

🇨🇦 Canada 🇰🇷 South Korea 🇺🇸 United States

Primary endpoints

Number of patients with dose limiting toxicities of 225Ac-ETN029; Incidence and severity of adverse events and serious adverse events of 225Ac-ETN029; Dose modifications for 225Ac-ETN029; Dose intensity for 225Ac-ETN029

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: 22 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