Phase 1 Endometrial 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:
- You are 18 years old or older and have been diagnosed (confirmed by tissue testing) with an advanced or spreading solid tumor, specifically one of these cancer types: prostate cancer that no longer responds to hormone treatment (including a specific subtype called neuroendocrine prostate cancer), hormone receptor-positive/HER2-negative breast cancer, colorectal cancer, cervical cancer, non-small-cell lung cancer, or recurring glioblastoma (brain tumor)
- You are able to understand and sign a consent form agreeing to take part in the study
- Your cancer has continued to grow or spread after trying at least 2 different treatments (this does not apply to recurring glioblastoma)
- If you have prostate cancer: you have had surgical or ongoing hormone treatment to lower testosterone, and your testosterone levels are very low (below a specific threshold)
- At least one of your tumors can be measured on a scan, and it shows uptake of a special imaging substance used in this trial (not required for glioblastoma)
- If you have prostate cancer without measurable soft tissue tumors, uptake of the imaging substance in bone tumors is acceptable (confirm with trial site)
- Your general health and ability to carry out daily activities meets a specific minimum level on a standard scale (rated 0 or 1, meaning fully active or able to do light activity); a score of 2 may be considered on a case-by-case basis
- Your blood, liver, and kidney function results are within acceptable ranges, including healthy enough levels of white blood cells, infection-fighting cells, platelets, haemoglobin, liver enzymes, bilirubin, kidney function, and pancreatic enzymes
- If you could become pregnant, or if your partner could become pregnant, you are willing to use reliable contraception or abstinence during the study and for a set period after your last treatment dose
- If you have recurring glioblastoma: your tumor has come back for the first or second time after standard treatment including radiation therapy, and at least 12 weeks have passed since completing that radiation; if you had surgery for the recurrence, it was completed at least 4 weeks before starting this trial's treatment with no complications
- If you have recurring glioblastoma: your tumor shows uptake of the imaging substance on a special scan, and shows a specific type of enhancement on an MRI scan at the time the recurrence was diagnosed
Who may not be able to join:
- The official criteria do not list specific exclusion criteria in the text provided; please confirm all exclusion criteria directly with the trial site (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.
Contact this trial
Phone: 469-638-0744
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
To determine the Recommended Phase 2 Dose (RP2D) of ²¹²Pb-DOTAM-GRPR1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.