Phase 2 Ovarian Cancer Trial, Recruiting NCT07435701 Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07435701
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 who are willing to sign a consent form and are able to follow the study schedule and procedures
  • Women between 18 and 75 years of age
  • People with a physical functioning level rated as 0, 1, or 2 on a standard medical scale called the ECOG scale, meaning they are able to carry out at least some daily activities (confirm with trial site)
  • People whose advanced ovarian cancer has been confirmed through tissue or cell testing
  • People whose cancer has either not responded to at least two previous standard treatments, who cannot tolerate standard treatments, or for whom no standard treatment is available
  • People whose cancer is complicated by a large build-up of fluid in the abdomen (called malignant ascites), with a volume of at least 2,000 mL as shown on ultrasound or CT scan
  • People with an expected survival of at least 3 months
  • People whose blood counts and organ function (liver, kidneys, and blood clotting) meet specific minimum levels based on recent blood tests, without needing a blood transfusion or certain growth factor medications in the 14 days before enrolling
  • People whose side effects from previous treatments have mostly resolved to a mild level before joining (with some exceptions for hair loss and mild nerve-related side effects)

Who may not be able to join:

  • People who have previously received any type of cell therapy treatment
  • People whose abdominal fluid build-up appears to be divided into separate pockets or compartments, as seen on CT or ultrasound
  • People who have received any systemic anti-cancer treatment (such as chemotherapy or targeted therapy) within 3 weeks before the trial procedure
  • People who have taken Traditional Chinese herbal medicine with anti-cancer indications within 3 weeks before the trial procedure
  • People who have taken oral or injected corticosteroids at a dose of 10 mg per day of prednisone or equivalent, or other immune-suppressing medicines, within 2 weeks before the trial procedure (low-dose inhaled or topical forms may be allowed)
  • People who have had major surgery within 4 weeks before screening, or who have major surgery planned during the study
  • People who have had another type of cancer within the past 5 years (with some exceptions for certain low-risk skin cancers that have been fully treated)
  • People with a history of active or suspected autoimmune or inflammatory disease
  • People who have had an organ transplant or a bone marrow/stem cell transplant
  • People with certain active infections, including active Hepatitis B, active Hepatitis C, a current infection requiring antibiotic treatment, or HIV
  • People who have received a live or weakened live vaccine within 4 weeks before the trial procedure
  • People with serious heart or blood vessel conditions, including uncontrolled high blood pressure, recent heart attack or stroke, significant heart failure, or serious abnormal heart rhythms
  • People with severe lung disease or significantly reduced lung function based on breathing tests
  • People with a known significant neurological or psychiatric condition, such as epilepsy or dementia
  • People whom the trial doctors consider unsuitable for other medical reasons, including those who had severe reactions to immunotherapy in the past

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 22 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: Ning Li, MD, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: 8610-87787211

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
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Registry
ClinicalTrials.gov
Start date
5 January 2026
Est. completion
23 January 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of Adverse Events and Dose-Limiting Toxicities; RP2D

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: 22 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