The purpose of this study is to determine the response rate of gemcitabine, cisplatin and
erlotinib in metastatic pancreatic cancer.
Drug: Gemcitabine, Cisplatin, Erlotinib (Tarceva)
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Locations near you
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Full eligibility criteria for NCT00922896
Ages eligible for Study
18 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Age older than 18
Younger than 75
ECOG performance status 0 or 1
Histologically confirmed adenocarcinoma of the pancreas
Metastatic pancreatic cancer
No prior chemotherapy for metastatic pancreatic cancer
A patient with at least one measurable primary lesion of which the diameter is confirmed to be 10mm in Spiral CT or multidetector CT (MD CT)
A patient with no measurable disease
A patient who received previous palliative chemotherapy for pancreatic cancer
A patient with locally advanced pancreatic cancer
A patient who received adjuvant chemotherapy for pancreatic cancer within 1 year
A patient with previous active or passive immunotherapy
A pregnant or lactating patient
All locations for NCT00922896
Korea, Republic of (3)
Dong-A University Hospital
Busan, Korea, Republic of, 602-715
Gyeongsang Unversity Hospital
JinJU, Korea, Republic of
Chung-Ang University Hospital
Seoul, Korea, Republic of, 156-755
View full eligibility
Tris trial is registered with FDA with number: NCT00922896. The sponsor of the trial is Gyeongsang National University Hospital and it is looking for 22 volunteers for the current phase.
Official trial title: A Phase II Trial of Erlotinib in Combination With Gemcitabine and Cisplatin in Metastatic Pancreatic Cancer
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