Phase 2 Endometrial Cancer Trial, Recruiting NCT07594015 Sponsor: University of Miami Condition: Endometrial Cancer
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Phase 2 Endometrial Cancer Trial, Recruiting

NCT07594015
Recruiting Phase 2

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 recurrent endometrial cancer (a type of uterine cancer that has come back), confirmed by laboratory testing of tissue, including specific subtypes such as serous, endometrioid, carcinosarcoma, or clear cell.
  • People whose cancer has been tested and found to have a normal DNA repair system (called "mismatch repair proficient"), confirmed through laboratory testing.
  • People whose cancer has already been treated with a first round of chemotherapy (platinum-based) combined with immunotherapy, and that treatment has stopped working.
  • People who have had advanced genetic testing (called next-generation sequencing) done on their tumour, either from the original diagnosis or when the cancer came back.
  • People with a general health and activity level rated between 0 and 3 on a standard medical scale (ranging from fully active to capable of limited self-care — confirm with trial site for details).
  • People aged 18 years or older.
  • Women who are not able to become pregnant, or women who could become pregnant but agree to use contraception as required by the trial; participants must not be pregnant or breastfeeding at the time of joining.
  • People who have at least one area of cancer that can be measured on a scan, according to standard measurement guidelines.
  • People whose blood and organ function results meet minimum levels, including: sufficient red blood cells, white blood cells, and platelets; adequate kidney function; and liver chemical levels within an acceptable range (confirm with trial site for exact values).
  • People who are willing and able to provide written consent to participate.
  • People who have waited at least 3 weeks since finishing any previous cancer treatment before joining the trial.

Who may not be able to join:

  • People diagnosed with uterine sarcoma (a different type of uterine cancer).
  • People who have active cancer spread to the brain or the lining around the brain or spinal cord.
  • People who have had a serious allergic reaction in the past to pembrolizumab, lenvatinib, or any ingredients in those medicines.
  • People who have an active autoimmune disease (where the immune system attacks the body) that has required long-term steroid treatment for more than 3 months in the past 6 months.
  • People who are pregnant or breastfeeding at the time of joining the trial.
  • People who have previously been treated with lenvatinib or similar medicines that target a pathway called VEGFR.
  • People who are currently taking part in another clinical trial or receiving other cancer treatments, with the exception of hormonal therapy for breast cancer.
  • People who have another serious uncontrolled health condition, such as an active infection, that could affect safe participation in the trial.
  • People whose blood pressure has averaged above certain levels across their last three recorded measurements (confirm with trial site for exact thresholds).
  • People who have had a serious heart event within the past 12 months, such as a heart attack, unstable chest pain, or significant heart failure.
  • People who have had an organ transplant or who take immune-suppressing medicines in a way that could interfere with the trial treatments.
  • People who have had another type of cancer in the past 2 years, except for certain common skin cancers (non-melanoma skin cancer).

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 2: approximately ~30% 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: Navya Nair, MD, MPH, University of Miami

Phone: 305-243-2233

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 2
Registry
ClinicalTrials.gov
Start date
1 September 2026
Est. completion
1 September 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Clinical Benefit Rate

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