Phase 2 Endometrial Cancer Trial, Recruiting NCT06686043 Sponsor: Baylor College of Medicine Condition: Endometrial Cancer
Back to Endometrial Cancer

Phase 2 Endometrial Cancer Trial, Recruiting

NCT06686043
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 been diagnosed with locally advanced or metastatic cervical cancer (Stage IB2–IVB), vaginal cancer (Stage II–IVB), or vulvar cancer (Stage II–IVB), and surgery is not considered your primary treatment option.
  • Your cancer can be measured on imaging scans, and you have had a scan (CT or PET-CT) of your chest, abdomen, and pelvis within the past 56 days.
  • You are newly diagnosed with your cancer.
  • You are 18 years of age or older.
  • You are generally well enough to carry out light activity and care for yourself (your doctor will assess this using a standard scale).
  • Your blood counts, kidney function, and liver function are within acceptable ranges, based on a blood test taken within the past 28 days.
  • If you are HIV-positive, your immune cell count (CD4) is above 200 and you are consistently taking your HIV medications.
  • If you have had hepatitis B, the virus is undetectable in your blood while on treatment.
  • If you have had hepatitis C, you have been successfully treated and cured, or the virus is currently undetectable in your blood.
  • If you have had brain metastases (cancer spread to the brain), they have been treated and follow-up scans show no sign of the cancer growing there.
  • If you have or have had another type of cancer, it is unlikely to interfere with this study's treatment or results (confirm with trial site).
  • You are able to receive chemoradiation (combined chemotherapy and radiation therapy), and the tumor can be directly accessed for injection as part of the treatment.
  • If you are taking steroid medications, your dose has been stable for at least 4 weeks before starting the study treatment.
  • You are willing and able to understand the study and give written consent to participate.
  • You agree not to donate blood during the study or for 90 days after your last dose of treatment.
  • You agree not to breastfeed during the study.
  • If you could become pregnant, you have had a negative pregnancy blood test within 14 days before joining the study.

Who may not be able to join:

  • You are currently taking part in another clinical trial involving an experimental treatment.
  • You have untreated or worsening cancer that has spread to the brain or the lining around the brain.
  • You have had a serious allergic reaction to a drug that is chemically or biologically similar to the ones used in this study.
  • You have another serious illness that is not well controlled.
  • You have a mental health condition or personal circumstances that would make it difficult to follow the study's requirements.
  • You are currently pregnant.
  • You are currently breastfeeding.

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 15 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: Jan S Sunde, MD, Baylor College of Medicine

Phone: 832-826-8071

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
23 August 2024
Est. completion
23 August 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression free survival

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: 15 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