CORE: Capecitabine, Oxaliplatin, Radiotherapy and Excision

PHASE2CompletedINTERVENTIONAL
Enrollment

87

Participants

Timeline

Start Date

July 31, 2003

Primary Completion Date

November 30, 2007

Study Completion Date

November 30, 2007

Conditions
Rectal Neoplasms
Interventions
DRUG

Oxaliplatin, capecitabine, radiotherapy

"* Oxaliplatin 50mg/m² I.V. 2 hours weekly x 5 doses~* Capecitabine 825mg/m² P.O. B.I.D. daily x 5 days x 5 weeks~* Radiotherapy 45 Gy total (1.8Gy/dose) 25 fractions daily x 5 days x 5 weeks"

Trial Locations (7)

Unknown

Sanofi-Aventis Administrative Office, Diegem

Sanofi-Aventis Administrative Office, Paris

Sanofi-Aventis Administrative Office, Frankfurt

Sanofi-Aventis Administrative Office, Milan

Sanofi-Aventis Administrative Office, Pe Gouda

Sanofi-Aventis Administrative Office, Barcelona

Sanofi-Aventis Administrative Office, Guildford Surrey

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT00174616 - CORE: Capecitabine, Oxaliplatin, Radiotherapy and Excision | Biotech Hunter | Biotech Hunter