Phase 1 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:
- 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.
Contact this trial
Phone: 1-888-669-6682
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
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?
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.