Expired Study
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Baltimore, Maryland 21231


Purpose:

Research Hypothesis: Ipilimumab (an antibody that blocks negative signals to T cells) administered alone or in combination with a pancreatic cancer vaccine (allogeneic pancreatic tumor cells transfected with a GM-CSF gene), has an acceptable safety profile in subjects with locally advanced, unresectable or metastatic pancreatic adenocarcinoma. Primary Objective: To determine the safety profile of ipilimumab alone or in combination with a pancreatic cancer vaccine in subjects with locally advanced, unresectable or metastatic pancreatic adenocarcinoma. Secondary Objectives: - To estimate overall survival (OS) which will serve as the primary efficacy signal. - To explore an association of T cell responses and immunological responses with OS in patients receiving treatment. - To estimate overall response rate (ORR), immune related best overall response rate (irBOR), progression free survival (PFS), and duration of response in patients receiving treatment. - To explore an association between immune-related adverse events (IRAEs) and ORR. - To measure tumor marker kinetics (CA 19-9) in patients receiving treatment.


Criteria:

Inclusion Criteria: 1. Documented cancer of the pancreas who have failed (or are not candidates for) standard therapy 2. ECOG Performance Status of 0 to 1 3. Adequate organ function as defined by study-specified laboratory tests 4. Must use acceptable form of birth control through the study and for 28 days after final dose of study drug 5. Signed informed consent form 6. Willing and able to comply with study procedures Exclusion Criteria: 1. Currently have or have history of certain study-specified heart, liver, kidney, lung, neurological, immune or other medical conditions 2. Clinical metabolic or laboratory abnormalities defined as Grade 3 or 4 of the National Cancer Institute's (NCI's) Common Terminology Criteria for Adverse Events (CTCAE), version 3.0 3. Systemically active steroids 4. Another investigational product within 28 days prior to receiving study drug 5. Major surgery or significant traumatic injury (or unhealed surgical wounds) occurring within 28 days prior to receiving study drug 6. Infection with HIV, hepatitis B or C at screening 7. Pregnant or lactating 8. Conditions, including alcohol or drug dependence, or intercurrent illness that would affect the patient's ability to comply with study visits and procedures


NCT ID:

NCT00836407


Primary Contact:

Principal Investigator
Dung Le, MD
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21231
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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