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NCT07096583Active, not recruitingPhase 1/2

An Exploratory Study on NK Cell-assisted Prevention of Bone Marrow Suppression During Chemotherapy for Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 31 Jul 2025

Brief summary (registry, in English)

To evaluate the remission effect and safety of intravenous injection of METR-NK cells as adjuvant therapy on bone marrow suppression in patients with ovarian cancer after chemotherapy

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
24 Jul 2025
Start date
Jul 2025
Primary completion date
Jul 2026
Lead sponsor
Anhui Provincial Cancer Hospital
NCT number
NCT07096583

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 20
  • From Jul 2025 to the primary completion date, Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients had received drugs that were in other clinical trials or other cellular immunotherapies within 28 days before the screening period;

Other illness

  • Patients with other malignant tumours in the past five years.;
  • Acute illness is ongoing, or in the past 2 years with severe disease, such as active infection, cardiovascular disease or fever patients heart function (grade III or IV level), mental health problems (such as alcohol, drugs).;
  • Immunodeficiency disease, including HIV positive or suffering from other acquired and congenital immunodeficiency disease;
  • Organ transplantation, organ transplantation or organ failure patients undergoing immunosuppressive medication or long-term use of immunosuppressive drugs patients;
  • Move/vein thrombosis incidents happened in 6 months, such as cerebrovascular accident (including transient ischemic attack), deep vein thrombosis and pulmonary embolism;
  • subjects suffering from mental illness, including major depression, mania, epilepsy, dementia, etc;
  • Researchers say the other condition that doesn't fit into the group.

Lab values

  • In patients with known to METR NK preparation any component of the final product, including the human serum albumin;
  • Breastfeeding during screening serum or urine pregnancy test was positive in female;

Who the study is looking for

  • Age 18-70 years old (≥18, ≤70);
  • Confirmed by pathology of high grade serous ovarian cancer, high level of endometrial carcinoma, and/or primary peritoneal carcinoma fallopian tube carcinoma epithelial ovarian cancer;
  • ECOG score: 0-1;
  • before, during, and after treatment of blood specimen can obtain, and the participants agreed to expand blood samples to central laboratory for the trial research purposes.;
  • Expectations alive at least 3 months;
  • Laboratory examination indexes meet the following requirements
  • (1) renal function: Cr ULN or less (upper limit of normal) x 1.5, endogenous creatinine clearance rate (Ccr) or 60 ml/min;
  • (2) the liver function: the total bilirubin ULN x 1.5 or less; ALT and AST≤ULN×2.5; (If there is intrahepatic cholangiocarcinoma or liver metastasis, the total bilirubin level should be less than 3 times the upper limit of normal, and the aminotransferase level should be less than 5 times the upper limit of normal); The neutrophilic granulocyte count
  • Women of childbearing age agreed to during the study and research within 6 months after the end of contraception, And non-lactating patients;
  • Participants can understand the research situation and voluntarily signed informed consent. No serious complications such as active digestive tract hemorrhage, perforation, jaundice, gastrointestinal obstruction, non cancerous fever \> 38 ℃;
  • Expected, adherence to the good curative effect and adverse reaction will be effected according to the plan calls for follow-up

Age in the registry: 18 years to 70 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Anhui Cancer Hospitail
Coordinator of this site? Confirm its status
HefeiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.