Study of Pancreatic Enzyme Replacement on Completion of Adjuvant Chemotherapy for Resected Pancreatic Adenocarcinoma

Stopped early · Phase 2

Conditions studied: Pancreatic Cancer

In brief

This research study is evaluating a study drug to treat pancreatic exocrine insufficiency (PEI) during the first year after the diagnosis of pancreatic cancer while the participant is recovering from surgery and receiving adjuvant treatment. The study drug involved in this study is: -Zenpep

Key facts

Study ID

NCT03469258

Run by

Dana-Farber Cancer Institute

People needed

4

Starts

2018-04-13

Expected to finish

2019-10-01

Last updated by the study team

2020-08-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must have histologically or cytologically confirmed pancreatic ductal adenocarcinoma. Variants or mixed histology will be included if the predominant histology is adenocarcinoma.
• Participants must have potentially resectable pancreatic cancer defined as: (1) no detectable metastases (2) signed consent for attempted resection of pancreatic cancer per treating surgeon.
• ECOG performance status ≤2.
• Age >18 years. Participants <18 years old are excluded from this study because subsequent adjuvant therapy is based on therapy guidelines in the adult population.
• Willingness to consider adjuvant therapy following surgical resection of disease, signed in the consent form attestation.
• Ability to understand and willingness to provide written informed consent.
• Pre-operative laboratory values adequate to undergo resection of pancreatic cancer, as defined below:
• Hemoglobin > 7.0 g/dL;
• Platelets ≥ 40,000/mL;
• Creatinine < 2.5 mg/dL or; Creatinine clearance ≥ 20 mL/min/1.73 m2 for participants with creatinine levels above institutional normal.

You may not qualify if…

• Pancreatic resection not performed. Intraoperative findings and unforeseen medical exigent circumstances may preclude pancreatic resection. Such outcomes include undetected metastases or vascular involvement, which preclude resection with intent to cure, as well as perioperative medical events including cardiopulmonary complications.
• Final pathology other than pancreatic ductal adenocarcinoma or primary component other than adenocarcinoma.
• Any prior chemotherapy and/or radiation for pancreatic cancer at the time of study enrollment, including neoadjuvant chemotherapy and/or radiation therapy.
• Second malignancy with active disease.
• History of allergic reactions or hypersensitivity attributed to compounds of similar chemical or biologic composition to pancrelipase
• Pregnant women are excluded from this study because subsequent adjuvant therapy needed for the primary endpoint is teratogenic. Pancrelipase is category C. Animal reproduction studies have not been conducted on pancrelipase and minimal data is available.
• Participants unable to self-administer pancrelipase.
• Uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Participants who are receiving any other investigational agents.
• Participant unable to tolerate oral nutrition.

Where it is running

• Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.