Phase 2 Endometrial Cancer Trial, Recruiting NCT05247268 Sponsor: Fudan University Condition: Endometrial Cancer
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Phase 2 Endometrial Cancer Trial, Recruiting

NCT05247268
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:

  • You have agreed to take part and signed a consent form
  • You have been diagnosed with early-stage endometrial cancer (a specific low-risk type called endometrioid, grade 1, that has not grown into the muscle wall of the uterus), confirmed through a biopsy or similar procedure
  • Scans (such as MRI, CT, or ultrasound) show no signs that the cancer has spread into the uterus muscle wall or to other parts of the body
  • You strongly wish to keep your uterus and/or ability to have children
  • You are willing and able to attend regular follow-up appointments at the Obstetrics and Gynecology Hospital of Fudan University

Who may not be able to join:

  • Test results suggest the cancer has grown deeper into the uterus wall or spread outside the uterus
  • Your endometrial cancer has come back after previous treatment
  • You have a serious illness or significantly reduced liver or kidney function
  • You have a different type of endometrial cancer, another cancer of the reproductive system, breast cancer, or another type of cancer that is affected by hormones and cannot be treated with progesterone
  • Your condition requires surgical removal of the uterus or a treatment other than medication
  • You are known or suspected to be pregnant
  • You have a medical reason why you cannot take the medications used in this trial (Medroxyprogesterone Acetate, Megestrol Acetate, Triptorelin Acetate, or Letrozole) (confirm with trial site)
  • You have had any hormone-based treatment in the 3 months before joining the trial
  • You have had a serious condition such as a stroke or heart attack, or have a history of blood clots
  • You smoke more than 15 cigarettes per day

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 19 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.

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
11 March 2022
Est. completion
10 March 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response rates within 16 weeks of treatment

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: 19 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