Phase 1 Endometrial Cancer Trial, Recruiting NCT06191133 Sponsor: Lindsay Ferguson, MD Condition: Endometrial Cancer
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Phase 1 Endometrial Cancer Trial, Recruiting

NCT06191133
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:

  • People who have been confirmed by tissue or cell testing to have high-grade abnormal cells (dysplasia) or cervical cancer, specifically of the squamous cell, adenocarcinoma, or adenosquamous cell carcinoma types
  • People whose condition is being managed with one of these procedures: a LEEP (a procedure to remove abnormal cervical tissue using a wire loop), a cone biopsy (CKC), a hysterectomy (removal of the uterus), or a combination of chemotherapy and radiation
  • People aged 18 years or older
  • People with normal liver function, as confirmed by standard blood tests
  • People who speak English
  • People who are able to understand the trial and are willing to sign a consent form

Who may not be able to join:

  • People with active liver disease, including primary biliary cirrhosis or unexplained abnormal liver blood test results
  • People with severe kidney impairment or who are on dialysis for end-stage kidney disease
  • People with pre-existing gallbladder problems, including active gallstones
  • People with a known allergy or sensitivity to fenofibrate or fenofibric acid (a type of medication)
  • People who are pregnant or breastfeeding, due to unknown risks to the baby or infant — note that the trial site screens people who could potentially become pregnant for pregnancy before any procedures and again before treatment begins

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 16 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

Principal Investigator: Lindsay Ferguson, MD, University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

Phone: 216-844-3954

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
Lindsay Ferguson, MD
Registry
ClinicalTrials.gov
Start date
20 November 2024
Est. completion
30 June 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change in p53 levels; Change in tumor metabolic status

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: 16 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