Phase 3 Endometrial Cancer Trial, Recruiting NCT07166094 Sponsor: Genmab Condition: Endometrial Cancer
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Phase 3 Endometrial Cancer Trial, Recruiting

NCT07166094
Recruiting Phase 3 🇦🇺 Australian site

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 endometrial cancer (any type except neuroendocrine tumors, carcinosarcoma, or endometrial sarcoma) that has come back or continued to grow, confirmed by laboratory testing of tissue or cells.
  • People who have received at least 1 but no more than 3 prior rounds of treatment for their cancer.
  • People whose prior treatment included both a platinum-based chemotherapy and an immunotherapy drug called a PD-(L)1 inhibitor (these may have been given separately or together).
  • People whose cancer came back more than 12 months after finishing platinum-based chemotherapy may need to have received platinum-based chemotherapy again for the returning cancer, unless the treating doctor has documented a medical reason why that was not possible (confirm with trial site for details on exceptions).
  • People whose cancer has been confirmed on scans to have grown or spread after their most recent treatment.

Who may not be able to join:

  • People who have previously received a type of treatment called an antibody-drug conjugate that contains a topoisomerase 1 inhibitor.
  • People who have, or have had, another cancer in addition to their endometrial cancer, unless that other cancer carries a very low risk of spreading or causing death, has been fully treated, or has been in complete remission for 3 or more years (specific exceptions apply — confirm with trial site).
  • People with active cancer spread to the brain or the lining of the brain and spinal cord, although people whose brain metastases have already been treated and have been stable for at least 4 weeks, with no new or growing spots and no longer taking steroids or anti-seizure medications for at least 7 days, may still be considered (confirm with trial site).
  • People who have been hospitalised due to a bowel blockage recently, have symptoms of a bowel blockage, or whose scans show a bowel blockage at the time of screening.
  • People who currently require nutrition delivered directly into the bloodstream (intravenous nutrition) may need special review by the trial medical team to determine whether participation is possible (confirm with trial site).

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 26 July 2026
Phase 3: approximately ~65% 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: Study Official, Genmab

Phone: +4570202728

Australian sites

GenesisCare Campbelltown, Campbelltown, New South Wales
Chris O'Brien Lifehouse, Camperdown, New South Wales
Calvary Mater Newcastle, Waratah, New South Wales

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 3
Sponsor
Genmab
Registry
ClinicalTrials.gov
Start date
28 November 2025
Est. completion
1 August 2029

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇨🇦 Canada 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇯🇵 Japan 🇱🇹 Lithuania 🇳🇴 Norway 🇵🇱 Poland Puerto Rico 🇸🇬 Singapore 🇪🇸 Spain 🇺🇸 United States

3 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Progression-free Survival (PFS) per Response Criteria in Solid Tumors (RECIST) v1.1, as Determined by Blinded Independent Central Review (BICR); Overall Survival (OS)

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: 26 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