A Study of Capecitabine (Xeloda) and Peginterferon Alfa-2a (Pegasys) in Treatment-Naive Participants With Advanced Liver Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

January 31, 2005

Primary Completion Date

November 30, 2008

Study Completion Date

November 30, 2008

Conditions
Carcinoma, Hepatocellular
Interventions
DRUG

Capecitabine

Participants will receive oral capecitabine, 1000 mg/m\^2 twice daily on Days 1 to 14 of each 21-day cycle, for at least 6 cycles (18 weeks). Treatment may continue until disease progression, intolerable toxicity, or consent withdrawal.

DRUG

Peginterferon alfa-2a

Participants will receive SC peginterferon alfa-2a, 180 mcg every week during each 21-day cycle, for at least 6 cycles (18 weeks). Treatment may continue until disease progression, intolerable toxicity, or consent withdrawal.

Trial Locations (8)

333

Kueishan

704

Tainan City

10400

Bangkok

10700

Bangkok

50202

Chiang Mai

90112

Songkhla

100050

Beijing

510060

Guangzhou

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT02576964 - A Study of Capecitabine (Xeloda) and Peginterferon Alfa-2a (Pegasys) in Treatment-Naive Participants With Advanced Liver Cancer | Biotech Hunter | Biotech Hunter