Phase 1 Endometrial Cancer Trial, Recruiting NCT05283330 Sponsor: Orano Med Theranostics, SAS Condition: Endometrial Cancer
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Phase 1 Endometrial Cancer Trial, Recruiting

NCT05283330
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:

  • 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.

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 21 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: 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

Status
Recruiting
Phase
Phase 1
Sponsor
Orano Med Theranostics, SAS
Registry
ClinicalTrials.gov
Start date
22 December 2022
Est. completion
1 January 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

To determine the Recommended Phase 2 Dose (RP2D) of ²¹²Pb-DOTAM-GRPR1

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: 21 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