Phase 3 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:
- You are generally healthy and able to carry out normal daily activities with little or no limitations (this is measured on a standard scale called ECOG 0-1)
- You have been diagnosed with endometrial (uterine) cancer that has been confirmed by a lab test, and your cancer has a specific genetic feature called "TP53 wild type" (TP53WT) — this means a certain gene in your cancer is in its normal form
- If your cancer has spread or come back, you must have completed one course of chemotherapy (up to 6 cycles) using specific drugs called taxane and platinum, and your cancer must have responded well to that treatment (shrunk or disappeared), as measured by standard medical guidelines
- Your blood, liver, and kidney functions are at healthy enough levels, checked within the last 14 days
Who may not be able to join:
- Your cancer is a sarcoma or a specific type called small-cell carcinoma with neuroendocrine features
- You have received immunotherapy, cytokine therapy, or any experimental treatment within the last 28 days
- You currently have a surgical drain tube left in your body
- You have a significant heart rhythm problem involving something called a prolonged QTc interval (Grade 2 or higher) — (confirm with trial site)
- You have previously had a major organ transplant (such as a kidney, liver, or heart)
- You have a history of serious bleeding problems, a major bleed, or bleeding in the brain within the last 24 weeks
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
Phone: 650-542-0136
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
Part 1: To determine the navtemadlin Phase 3 dose; Part 2: To compare progression-free (PFS) survival by independent review committee (IRC) between navtemadlin and placebo
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.