Phase 2 Study of S-1 in Combination With Cisplatin as 1st Line Therapy in Advanced Non-Small Cell Lung Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

February 28, 2005

Primary Completion Date

October 31, 2006

Study Completion Date

July 31, 2007

Conditions
Advanced Non-Small Cell Lung Cancer
Interventions
DRUG

S-1

All patients will receive S-1 orally at a dose of 25 mg/m2 twice daily (BID) for 14 days followed by a 1-week recovery period, repeated every 3 weeks. The study may go to the third stage only if 7/31 (23%) or more patients have achieved a confirmed response (CR or PR) in stages 1 and 2 combined.

All Listed Sponsors
collaborator

Quintiles, Inc.

INDUSTRY

collaborator

United BioSource, LLC

INDUSTRY

lead

Taiho Oncology, Inc.

INDUSTRY

NCT00651833 - Phase 2 Study of S-1 in Combination With Cisplatin as 1st Line Therapy in Advanced Non-Small Cell Lung Cancer | Biotech Hunter | Biotech Hunter