Phase 2 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:
- People who have been diagnosed with a specific type of uterine cancer called endometrioid endometrial adenocarcinoma, confirmed by a biopsy or tissue sample taken within the past 8 weeks
- People aged 18 or older
- Women with this type of uterine cancer (any grade or stage) for whom surgery to remove the uterus is planned and considered appropriate
- People who have had a physical examination within roughly 6 weeks before the planned surgery
- People whose general health and ability to carry out daily activities falls within an acceptable range on a standard medical scale (ECOG score of 0, 1, 2, or 3), assessed within 28 days before joining
- People whose biopsy tissue has been preserved and stored in a way that makes it available for the study team to use
- People with blood counts, kidney function, and liver function results within the required ranges (confirm specific values with the trial site)
- People who have given written consent to participate and agreed to allow their health information to be shared for the study
- People of childbearing potential who have a negative pregnancy test before entering the trial
Who may not be able to join:
- People whose uterine cancer is a different type, such as serous, clear cell, carcinosarcoma, or a mixed type — only endometrioid adenocarcinoma is eligible
- People who received certain hormone-based treatments (progestins or anti-estrogen therapy) in the 3 months before their cancer diagnosis was confirmed (estrogen-only therapy is allowed)
- People whose general health falls into the most severely limited category on the standard medical scale (ECOG score of 4)
- People who have had a blood clot in a deep vein or in the lungs within the past 2 years, or who have an ongoing clotting disorder
- People who have previously received any treatment for uterine cancer, including surgery, radiation, or systemic therapy
- People whose stored biopsy tissue sample is too small or unavailable for the study
- People with a known or suspected peanut allergy
- People with serious other health conditions, a bowel blockage, or a condition affecting how the body absorbs food or medication, that would prevent them from taking tablets or capsules by mouth
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.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
Tissue response to progestin therapy
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.