OSI-906 With Gemcitabine and Erlotinib for Metastatic Ductal Adenocarcinoma of the Pancreas

Withdrawn before enrolling · Phase 1/Phase 2

Conditions studied: Pancreatic Cancer, Metastatic

In brief

OSI-906 is a new drug that may stop cancer cells from growing abnormally. This drug has been used in other research studies and information from those suggests that OSI-906 may help block cell receptors involved in tumor growth. Gemcitabine and erlotinib are used as standard treatment for pancreatic cancer. In this research study, the investigators are looking for the highest dose of OSI-906 that can be given safely in combination with gemcitabine and erlotinib. This dose will then be given together with gemcitabine and erlotinib to a further group of patients with pancreatic cancer.

Key facts

Study ID

NCT01600807

Run by

Dana-Farber Cancer Institute

People needed

0

Last updated by the study team

2013-06-26

Who can join

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

You may qualify if…

• Metastatic pancreatic ductal adenocarcinoma
• Measurable disease
• Life expectancy > 12 weeks
• Normal organ and marrow function
• Fasting blood glucose </= 150 mg/dL
• Able to swallow pills

You may not qualify if…

• Prior chemotherapy or radiotherapy for treatment of pancreatic cancer
• Receiving any other experimental agent
• Known brain metastases
• History of allergic reaction attributed to compounds of similar chemical or biologic composition to gemcitabine, erlotinib, or OSI-906
• Impairment of gastrointestinal function or gastrointestinal disease (e.g., ulcerative disease, uncontrolled nausea, vomiting, or diarrhea)
• Use of enzyme-inducing anti-epileptic drugs
• Diabetes mellitus which requires the use of exogenous insulin for glucose control
• Major surgery within 4 weeks of the start of study treatment
• Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• Use of strong or moderate CYP1A2 inhibitors/inducers
• Pregnant or breast feeding
• History of a different malignancy unless disease-free for at least 3 years
• HIV positive

Where it is running

• Massachusetts General Hospital — Boston, Massachusetts, United States
• Dana-Farber Cancer Institute — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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