45
Participants
Start Date
September 30, 2007
Primary Completion Date
November 30, 2010
Study Completion Date
June 30, 2013
Gemcitabine
1000 mg/m\^2, intravenous, Days 1, 8, 15 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.
Erlotinib
150 mg, taken orally, once a day, Days 1-28 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.
Sorafenib
400 mg, taken orally, twice a day, Days 1-28 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.
Bellevue Hospital, New York
New York University Cancer Center, New York
Desert Regional Medical Center, Palm Springs
Collaborators (2)
Bayer
INDUSTRY
OSI Pharmaceuticals
INDUSTRY
NYU Langone Health
OTHER