Endometrial Cancer Trial, Recruiting NCT07224464 Sponsor: New Phase Ltd. Condition: Endometrial Cancer
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Endometrial Cancer Trial, Recruiting

NCT07224464
Recruiting Not Applicable

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:

  • Doctors expect you to live for at least 90 days.
  • You have been diagnosed (confirmed by a tissue sample/biopsy) with an advanced cancer that has spread, located somewhere between your upper chest and pelvis, and it has continued to grow after standard treatments and cannot be removed by surgery or other local treatments.
  • Your cancer can be measured on a scan using a standard medical measurement system (called RECIST 1.1).
  • Your cancer has continued to grow despite standard available treatments, or you were unable to tolerate those treatments, and it cannot be cured.
  • Any side effects from your previous cancer treatments have fully cleared up, and at least 14 days have passed since your last cancer treatment or radiotherapy.
  • A scan (CT, MRI, or PET/CT) has confirmed your cancer has continued to grow since your last treatment.
  • You have no history of cancer spreading to the brain, confirmed by a scan taken within 30 days before starting treatment.
  • You have had a CT scan for treatment planning done within 14 days before starting the study treatment.
  • You are 18 years of age or older.
  • The measurement around your rib cage is 90 cm (about 35.5 inches) or less.
  • You are generally well enough to carry out some daily activities (confirm with trial site regarding the specific fitness level required).
  • Your blood, liver, and kidney functions meet certain minimum levels measured by blood tests on the day of screening and the day of the procedure.
  • You are able and willing to sign a written consent form agreeing to take part.
  • You do not have any electronic devices, electrically conductive implants, or metal objects inside your body, confirmed by a CT scan review and a questionnaire you complete.

Who may not be able to join:

  • You have received chemotherapy, radiotherapy, or hormonal therapy within the last 14 days before screening.
  • You have received immunotherapy, biological therapy, or any other experimental treatment within the last 21 days before screening.
  • You are still experiencing side effects from previous cancer treatments that are more than mild in severity.
  • You currently have cancer that has spread to the brain, or you have a prior history of cancer spreading to the brain.
  • You have a known history of allergic reactions to similar types of compounds used in this study (confirm with trial site for specific details).
  • You have another serious illness that is not under control — such as an active infection, heart problems, or a mental health condition — that the study doctor believes could put you at risk or make it hard for you to follow the study requirements.
  • You are currently pregnant or breastfeeding.
  • You are unwilling to abstain from sex or use contraception for up to 30 days after your last study treatment.
  • You have any electronic devices, electrically conductive implants, or metal objects inside your body.
  • Your rib cage circumference is more than 90 cm (about 35.5 inches).
  • You are unable to sign a written consent form.
  • You are unable to lie flat on your back with your arms extended above your head.

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 8 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Scott C Lester, MD, Mayo Clinic, Rochester, MN

Phone: +972-3-6798687

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
Not Applicable
Sponsor
New Phase Ltd.
Registry
ClinicalTrials.gov
Start date
16 December 2025
Est. completion
1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Primary safety profile: assessing the number of device related adverse events and serious adverse events.; Primary safety of recommended dose: characterization of protocol dosing regimen

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: 8 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