Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 1:16 PM
Ignite Modification Date:
2025-12-26 @ 1:16 PM
NCT ID:
NCT03362606
Eligibility Criteria:
Inclusion Criteria:
1. Written, informed consent obtained prior to any study-specific procedures.
2. Age older than 10 years.
3. Eastern Cooperative Oncology Group (ECOG) PS of 0 or 1.
4. Expected survival ≥ 12 weeks.
5. Histologically confirmed and documented high risk International Federation of Gynecology and Obstetrics (FIGO): Stage II-IV.
6. Not pregnant, and on appropriate birth control if of childbearing potential.
7. Initial hematopoietic reconstitution with
* neutrophils (ANC) ≥ 1,000/mm\^3;
* platelet (PLT) ≥ 100,000/mm\^3.
8. Proper renal and hepatic functions (ULN denotes "upper limit of normal range") with
* serum creatinine ≤ 2×ULN;
* serum bilirubin ≤ 2×ULN;
* AST/ALT ≤ 2×ULN;
* ALKP ≤ 5×ULN;
* serum bilirubin. 2.0 is acceptable in the setting of known Gilbert's syndrome.
9. Human immunodeficiency virus (HIV) and Hepatitis C virus (HCV) test were negative.
Exclusion Criteria:
1. Patients with ovarian tumors with low malignant potential (i.e. borderline tumors);
2. Patients with evidence of abdominal free air not explained by paracentesis or recent surgical procedure (prior, current or planned treatment).
3. Previous treatment of adoptive T cell therapy.
4. Current or recent treatment (within the 28-day period prior to Day 0) with another investigational drug
5. Minor surgical procedures within 2 days prior to Day 0 (including central venous access device placement for chemotherapy administration, tumor biopsies, needle aspirations).
6. Pregnant or lactating females.
7. Inadequate bone marrow function with
* absolute neutrophil count \< 1,000/mm\^3;
* platelet count \< 100,000/mm\^3;
* Hb \< 9 g/dL.
8. Inadequate liver and renal function with
* serum (total) bilirubin \> 1.5 x ULN;
* AST \& ALT \> 2.5 x ULN (\> 5 x ULN in patients with liver metastases);
* alkaline phosphatase \> 2.5 x ULN;
* serum creatinine \>2.0 mg/dl (\> 177 μmol/L);
* urine dipstick for protein uria should be \< 2+. Patients with ≥ 2+ proteinuria on dipstick urinalysis at baseline should undergo 24 hour urine collection and must demonstrate \< 1 g of protein/24 hr.
9. Serious active infection requiring i.v. antibiotics at during screening.
10. Subject infected with HCV (HCV antibody positive), HBV (HBsAg positive), and HIV (HIV antibody positive),Treponema pallidum antibody positive or TB culture positive.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
10 Years
Maximum Age:
80 Years
Study:
NCT03362606
Study Brief:
Protocol Section:
NCT03362606