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MOSAIC - Multicenter International Study of Oxaliplatin/ 5FU-LV in the Adjuvant Treatment of Colon Cancer
This study has been completed.
Study NCT00275210   Information provided by Sanofi-Aventis
First Received: January 3, 2006   Last Updated: April 17, 2009   History of Changes

January 3, 2006
April 17, 2009
October 1998
April 2003   (final data collection date for primary outcome measure)
  • To to detect occurrence of relapse the following examinations have to be performed for 5 years:
  • Every 6 months for ultrasound or abdominopelvic CT scan and CEA determination,
  • Every year for chest X-ray and colonoscopy for non polyp free patient,
  • Every 3 years colonoscopy for polyp free patient
Same as current
Complete list of historical versions of study NCT00275210 on ClinicalTrials.gov Archive Site
Every 2 weeks clinical and laboratory tests (hematological, creatinine and liver tests) for safety evaluation during treatment then every 6 months neurological examination Date of death for OS
Same as current
 
MOSAIC - Multicenter International Study of Oxaliplatin/ 5FU-LV in the Adjuvant Treatment of Colon Cancer
Multicenter International Study of Oxaliplatin/ 5FU-LV in the Adjuvant Treatment of Colon Cancer

To evaluate the FOLFOX regimen versus LV5FU2 in the adjuvant treatment of stage II and III colon cancer.

Primary objective: Disease Free Survival (DFS) Secondary objective: Overall Survival (OS), safety (including long term toxicity)

 
Phase III
Interventional
Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Colonic Neoplasms
Drug: Oxaliplatin (SR96669)
 
Andre T, Boni C, Mounedji-Boudiaf L, Navarro M, Tabernero J, Hickish T, Topham C, Zaninelli M, Clingan P, Bridgewater J, Tabah-Fisch I, de Gramont A; Multicenter International Study of Oxaliplatin/5-Fluorouracil/Leucovorin in the Adjuvant Treatment of Colon Cancer (MOSAIC) Investigators. Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer. N Engl J Med. 2004 Jun 3;350(23):2343-51.

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
2246
April 2003
April 2003   (final data collection date for primary outcome measure)

Main selection criteria:

  • Histologically proven stage Dukes " B2 " (stage II: T3-T4 N0 M0) and " C " (stage III: any T N1-2 M0) colon carcinoma. The inferior pole of the tumor must be above the peritoneal reflection (> 15 cm from the anal margin)·
  • Complete resection of the primary tumor without gross or microscopic evidence of residual disease
  • Treatment within 7 weeks following surgery
  • Age 18-75 years old
  • ECOG PS £ 2
  • No prior chemo, immuno or radiotherapy
Both
18 Years to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
Australia,   Austria,   Belgium,   Denmark,   France,   Germany,   Greece,   Hungary,   Israel,   Italy,   Netherlands,   Norway,   Poland,   Portugal,   Singapore,   Spain,   Sweden,   Switzerland,   United Kingdom
 
NCT00275210
ICD Study Director, sanofi-aventis
EFC3313
Sanofi-Aventis
 
Study Chair: Aimery de Gramont, MD Hopital saint-Antoine, Oncology department
Sanofi-Aventis
April 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP