A Study of Capecitabine (Xeloda) in Participants With Locally Advanced or Metastatic Pancreatic Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

March 31, 2003

Primary Completion Date

September 30, 2006

Study Completion Date

September 30, 2006

Conditions
Pancreatic Cancer
Interventions
DRUG

Capecitabine

Capecitabine will be administered orally at 830 mg/m\^2 BID (equivalent to a total daily dose of 1660 mg/m\^2) as intermittent treatment (given days 1 to 21 q4w).

DRUG

Gemcitabine

Gemcitabine will be administered at a dose of 1000 mg/m\^2 once weekly via IV infusion as intermittent treatment (repeated 4-week cycles of 3 weeks treatment and 1 week rest).

Trial Locations (7)

420-021

Buchun

Unknown

Daegu

Seoul

135-720

Seoul

137-702

Seoul

138-736

Seoul

158-710

Seoul

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT02565641 - A Study of Capecitabine (Xeloda) in Participants With Locally Advanced or Metastatic Pancreatic Cancer | Biotech Hunter | Biotech Hunter