Phase 2 Endometrial Cancer Trial, Recruiting NCT06157151 Sponsor: Precigen, Inc Condition: Endometrial Cancer
Back to Endometrial Cancer

Phase 2 Endometrial Cancer Trial, Recruiting

NCT06157151
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 aged 18 years or older.
  • People who have cervical cancer that has come back or spread to other parts of the body, confirmed by a tissue or cell sample.
  • People who have already received treatment with a medicine called pembrolizumab (either alone or combined with other treatments) for at least 6 weeks.
  • People whose cervical cancer has tested positive for HPV (Human Papillomavirus), confirmed by a tissue or cell sample.
  • People who have at least one area of cancer that can be measured using standard imaging guidelines (called RECIST v1.1).
  • People who are reasonably active and able to care for themselves, rated 0 or 1 on a standard health and activity scale (confirm with trial site).
  • People who are expected to live for at least 12 weeks from the time of joining the trial.
  • People whose liver, kidneys, and other organs are working well enough (confirm with trial site for specific requirements).
  • Women who could become pregnant must have a negative pregnancy blood test before starting, and must agree to use reliable contraception during the trial and for at least 6 months after finishing treatment.
  • People who are able to understand the trial information and are willing to sign a consent form.

Who may not be able to join:

  • People who have had chemotherapy or targeted therapy within the last 14 days, or a monoclonal antibody treatment within the last 4 weeks, or who still have unresolved side effects from previous treatments.
  • People with a weakened immune system, an active autoimmune disease being treated with immune-suppressing medicines, or who have taken immune-suppressing medicines within the last 7 days. (People with HIV may still be considered if their condition is well controlled — confirm with trial site.)
  • People who have had active Hepatitis B or Hepatitis C infection within 30 days before joining.
  • People with a history of lung inflammation or scarring of the lungs that was not caused by an infection.
  • People with a history of autoimmune diseases affecting hormone-producing glands — with exceptions for people who have been successfully treated for Graves' disease, or who have an underactive thyroid managed with replacement medication (confirm with trial site).
  • People who have received a live vaccine within 30 days before the first dose.
  • People who have had another active cancer within the past year.
  • People who have a known cancer affecting the brain or central nervous system.
  • People who have had a severe allergic reaction (Grade 3 or higher) to pembrolizumab or any of its ingredients.
  • People with a known history of active tuberculosis (TB).
  • People who are pregnant or breastfeeding.
  • People who have had a solid organ transplant (such as a kidney, liver, or heart transplant).
  • People who are currently taking part in another clinical trial involving an experimental treatment or device, or who have done so within the last 4 weeks.
  • People who, in the opinion of the trial doctor, may have difficulty following the trial's monitoring and visit requirements.

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

Phone: 3015569900

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
Sponsor
Precigen, Inc
Registry
ClinicalTrials.gov
Start date
11 November 2025
Est. completion
11 November 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Determine the Objective Response Rate (ORR) following treatment with PRGN-2009 in combination with pembrolizumab in patients with pembrolizumab-resistant recurrent or metastatic cervical cancer.

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