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:
- Adults aged 18 or older
- People who have received a pathology diagnosis within the past 4 months of either low-grade (grade 1) uterine cancer of a specific type (endometrioid endometrial adenocarcinoma) or a pre-cancerous uterine condition called EIN (endometrial intraepithelial neoplasia)
- People whose diagnosis was made at a different hospital or clinic — the trial site will review those records before confirming eligibility
- People whose general physical functioning falls within an accepted range on a standard medical scale (ECOG score 0–3, meaning anywhere from fully active to limited in self-care — confirm with trial site)
- For those with uterine cancer: people whose cancer has not spread outside the uterus or into the uterine wall, as confirmed by MRI or internal ultrasound
- People with a BMI of 30 or higher, AND at least one of the following: significant other health conditions that make surgery higher risk (as assessed by a doctor), or a desire to preserve fertility
- People who have had appropriate breast screening and examinations suitable for their age before joining the trial, as confirmed in their medical records
- People who are willing to provide written consent and agree to follow all trial procedures
Who may not be able to join:
- People with a higher-grade (grade 2 or 3) uterine cancer, or a different type of uterine cancer such as clear cell or serous carcinoma
- People whose doctor suspects the cancer may have spread, or where imaging has confirmed it has spread
- People with abnormal cervical screening results
- People who have been diagnosed with thyroid cancer, pancreatitis, or a condition called multiple endocrine neoplasia syndrome type 2
- People who are currently pregnant or breastfeeding
- People with a personal history of medullary thyroid cancer
- People with a current or past history of cancers that are sensitive to hormones, such as certain breast cancers or melanoma
- People who have already been taking a class of medications called GLP-1 receptor agonists (used for diabetes or weight management) for more than 14 days at the time of joining the trial
- People who have had a hormonal IUD (levonorgestrel-releasing intrauterine device) in place for more than 45 days before joining the trial
- People who have more than one active cancer at the time of joining (some exceptions may apply at the treating doctor's or principal investigator's discretion)
- People with other serious medical conditions, including severe heart failure (NYHA Class IV), that a treating doctor considers would make the trial treatment unsafe or affect the reliability of results
- People who are prisoners, involuntarily detained, or held for compulsory psychiatric or physical health treatment
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
Principal Investigator: Kaitlin Nicholson, MD, University of Florida
Phone: 352-273-3650
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
Time from start of GLP-1RA to clearance of staging hysterectomy; Time from start of GLP-1RA to clearance for pregnancy pursuit; Endometrial pathologic response; Endometrial pathologic response
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.