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:
2025-12-24 @ 4:50 PM
Ignite Modification Date:
2025-12-24 @ 4:50 PM
NCT ID:
NCT01905150
Eligibility Criteria:
Inclusion Criteria:
* Patients must have histologically and cytologically confirmed metastatic (Stage IV), locally advanced unresectable (stage III), or locally recurrent pancreatic adenocarcinoma, with or without prior chemotherapy for their cancer.
* Eastern Cooperative Oncology Group (ECOG) performance status being 0-2.
* Expected survival \>3 months.
* Patients 18 years of age and older of both genders.
* Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use accepted contraceptive methods (abstinence, intrauterine device \[IUD\], oral contraceptive or double barrier device) during the study, and must have a negative serum or urine pregnancy test within 2 weeks prior to treatment initiation.
* Fertile men must practice effective contraceptive methods during the study, unless documentation of infertility exists.
* At least 2 weeks must have elapsed from any prior surgery or hormonal therapy.
* Laboratory values ≤2 weeks must be:
* Adequate hematologic
* Adequate hepatic function
* Adequate renal function
* No evidence of active infection and no serious infections within the past month.
* Mentally competent, able to understand and willing to sign the informed consent form.
Exclusion Criteria:
* Patients under the age of 18.
* Locally advanced resectable disease from pancreatic cancer
* Previous radiotherapy for cerebral metastases, central nervous system (CNS) or epidural tumor.
* Patients receiving any other standard or investigational treatment for their cancer, or any other investigational agent for any non-cancer indication within the past 4 weeks.
* Patients with any active uncontrolled bleeding, or a bleeding diathesis.
* Pregnant women, or women of child-bearing potential not using reliable means of contraception.
* Lactating females.
* Fertile men unwilling to practice contraceptive methods during the study period.
* Life expectancy less than 3 months.
* Any condition or abnormality which may, in the opinion of the investigator, compromise the safety of patients.
* Unwilling or unable to follow protocol requirements.
* Active heart disease including but not limited to symptomatic congestive heart failure, symptomatic coronary artery disease, symptomatic angina pectoris, symptomatic myocardial infarction, or symptomatic congestive heart failure.
* Patients with a history of myocardial infarction that is \< 3 months prior to registration.
* Patients with any amount of clinically significant pericardial effusion.
* Evidence of active serious infection.
* Patients with known HIV infection.
* Requirement for immediate palliative treatment of any kind including surgery and radiation.
* Patients that have received a chemotherapy regimen requiring stem cell support in the previous 6 months.
* Any condition or abnormality which may, in the opinion of the investigator, compromise the safety of the patient.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01905150
Study Brief:
Protocol Section:
NCT01905150