Phase 2 Study of Gemcitabine or Gemcitabine + Enzastaurin in Participants With Advanced or Metastatic Pancreatic Cancer
Completed · Phase 2
Conditions studied: Pancreatic Neoplasm
In brief
The purpose of this research study is to determine the effects and toxicity of gemcitabine alone or gemcitabine plus enzastaurin in participants with pancreatic cancer.
Key facts
- Study ID
- NCT00267020
- Run by
- Eli Lilly and Company
- People needed
- 130
- Starts
- 2005-12-01
- Expected to finish
- 2008-05-01
- Last updated by the study team
- 2020-08-31
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of adenocarcinoma of the pancreas.
- Pretreatment tumor specimen must be available.
- No prior chemotherapy immunotherapy, biological therapy, or hormonal therapy for pancreatic cancer, including 5-fluorouracil (5-FU) with radiation therapy.
- Prior radiation allowed.
- Ability to stop some types of anti-seizure medicines within 14 days of enrollment.
You may not qualify if…
- Endocrine pancreatic tumor or ampullary cancer.
- Central Nervous System (CNS) metastases.
- Inability to swallow tablets.
- 10% or greater weight loss over the 6 weeks before study entry.
Where it is running
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559), Mon - Fri, 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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