Phase 3 Cervical Cancer Trial, Recruiting NCT07061977 Sponsor: National Cancer Institute (NCI) Condition: Cervical Cancer
Back to Cervical Cancer

Phase 3 Cervical Cancer Trial, Recruiting

NCT07061977
Recruiting Phase 3

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 newly diagnosed with cervical cancer that has been confirmed by a tissue test (pathology), specifically one of these types: squamous cell carcinoma, adenocarcinoma, or adenosquamous cell carcinoma
  • People whose cervical cancer is locally advanced, meaning it has grown into nearby tissues and/or nearby lymph nodes, but has not spread to distant parts of the body (this covers certain specific stages, so the trial site can confirm which stages apply)
  • People whose cancer has not spread to lymph nodes in the upper part of the abdomen (above a specific spinal level known as T12/L1)
  • People who have not previously had their entire uterus removed (though removal of only part of the uterus for a reason unrelated to cervical cancer may still be acceptable — confirm with trial site)
  • People for whom a hysterectomy is not planned as part of their cervical cancer treatment
  • People who have not previously received surgery, radiation, or drug-based treatment for cervical cancer
  • People who have never received immunotherapy treatment
  • People who have never had radiation therapy to the pelvic area for any condition
  • People aged 18 or older
  • People who are well enough to carry out basic daily activities, based on a standard medical fitness scale (ECOG performance status of 2 or lower — confirm with trial site)
  • People who are not currently pregnant and not breastfeeding
  • People whose blood counts meet minimum levels: white blood cells, platelets, and red blood cells are all within required ranges (confirm specific values with trial site)
  • People whose kidneys are functioning well enough, based on a calculation of kidney filtration rate
  • People whose liver function blood test results are within acceptable ranges
  • People with a heart condition, if present, must be assessed as having heart function at a certain level or better on a standard heart health scale (confirm with trial site)
  • People who do not have an active infection that requires intravenous antibiotics
  • People who have not received a live vaccine (such as measles, mumps, rubella, chickenpox, yellow fever, rabies, BCG, or live nasal flu vaccine) within the 30 days before joining the trial — injected seasonal flu vaccines are generally acceptable
  • People who do not have an immune system disorder and are not taking immune-suppressing medications or steroids above a certain dose within 7 days before joining
  • People who do not have an active autoimmune disease that has needed systemic medical treatment in the past 2 years — hormone or other replacement therapies (such as thyroid or insulin) are generally acceptable
  • People who have no history of lung inflammation (pneumonitis) that required steroid treatment, and no current lung inflammation
  • People who have no known allergic reaction to the study drugs or to similar types of medications

Who may not be able to join:

  • People whose cervical cancer has spread to distant parts of the body
  • People whose cancer has spread to lymph nodes high in the abdomen (above the T12/L1 spinal level)
  • People who have already had their entire uterus removed
  • People for whom a hysterectomy is planned as part of their cervical cancer treatment
  • People who have previously received any treatment for cervical cancer (surgery, radiation, or systemic drug therapy)
  • People who have previously received immunotherapy
  • People who have previously had radiation to the pelvic area for any reason
  • People under 18 years of age
  • People whose general health and physical function fall below a certain level on the standard medical fitness scale
  • People who are currently pregnant or breastfeeding
  • People whose blood counts, kidney function, or liver function do not meet the required minimum levels
  • People with a heart condition assessed as below a certain level of heart function on the standard heart health scale
  • People with an active infection requiring intravenous antibiotics
  • People who have received a live vaccine within 30 days before joining the trial
  • People currently taking immune-suppressing medications or steroids above a certain dose
  • People with an active autoimmune disease that has required systemic treatment in the past 2 years
  • People with a history of lung inflammation that required steroids, or who currently have lung inflammation
  • People with a known allergy to the study drugs or closely related compounds

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 27 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.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
5 November 2025
Est. completion
31 December 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression free survival (PFS)

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: 27 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