Safety Study of Foretinib (GSK1363089) in Adults With Liver Cancer

PHASE1CompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

August 12, 2009

Primary Completion Date

March 7, 2012

Study Completion Date

March 24, 2015

Conditions
Carcinoma, Hepatocellular
Interventions
DRUG

Foretinib

Phase I starting dose 30 mg/day escalated to 45 mg/day; de-escalated to 30 mg/day. MTD for Phase II dose was 30 mg/day,

Trial Locations (7)

110

GSK Investigational Site, Taipei

112

GSK Investigational Site, Taipei

10400

GSK Investigational Site, Bangkok

10700

GSK Investigational Site, Bangkok

40002

GSK Investigational Site, Khon Kaen

70428

GSK Investigational Site, Tainan City

Unknown

GSK Investigational Site, Hong Kong

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT00920192 - Safety Study of Foretinib (GSK1363089) in Adults With Liver Cancer | Biotech Hunter | Biotech Hunter