62
Participants
Start Date
July 31, 2013
Primary Completion Date
August 31, 2015
Study Completion Date
August 31, 2015
Aflibercept
Pharmaceutical form: Concentrated solution (100 mg/4 mL \[25 mg/mL\], 200 mg/8 mL \[25 mg/mL\]) for infusion; Route of administration: Intravenous
Levofolinate
Pharmaceutical form: Solution for infusion (marketed formulation); Route of administration: Intravenous
Irinotecan
Pharmaceutical form: Solution for infusion (marketed formulation); Route of administration: Intravenous
5-FU
Pharmaceutical form: Solution for infusion (marketed formulation); Route of administration: Intravenous
Investigational Site Number 392011, Chiba
Investigational Site Number 392018, Chūōku
Investigational Site Number 392016, Fukuoka
Investigational Site Number 392017, Fukuoka
Investigational Site Number 392001, Kashiwa-Shi
Investigational Site Number 392019, Kawasaki-Shi
Investigational Site Number 392015, Matsuyama
Investigational Site Number 392013, Mitaka-Shi
Investigational Site Number 392004, Nagoya
Investigational Site Number 392006, Osaka
Investigational Site Number 392014, Sagamihara-Shi
Investigational Site Number 392008, Sapporo
Investigational Site Number 392003, Sendai
Investigational Site Number 392009, Shimotsuke-Shi
Investigational Site Number 392012, Shinjuku-Ku
Investigational Site Number 392005, Suita-Shi
Investigational Site Number 392002, Sunto-Gun
Investigational Site Number 392010, Tsukuba
Investigational Site Number 392007, Yufu-Shi
Lead Sponsor
Regeneron Pharmaceuticals
INDUSTRY
Sanofi
INDUSTRY