361
Participants
Start Date
November 30, 2013
Primary Completion Date
March 31, 2015
Study Completion Date
March 31, 2015
lixisenatide AVE0010
Pharmaceutical form:solution Route of administration: Subcutaneous injection
Investigational Site Number 392006, Adachi-Ku
Investigational Site Number 392005, Chiba
Investigational Site Number 392010, Chiyoda-Ku
Investigational Site Number 392003, Chuoh-Ku
Investigational Site Number 392004, Chūōku
Investigational Site Number 392015, Chūōku
Investigational Site Number 392012, Ebina-Shi
Investigational Site Number 392024, Higashiosaka-Shi
Investigational Site Number 392023, Kashiwara-Shi
Investigational Site Number 392008, Kawagoe-Shi
Investigational Site Number 392009, Kisarazu-Shi
Investigational Site Number 392002, Koganeishi
Investigational Site Number 392007, Koriyama-Shi
Investigational Site Number 392011, Mitaka-Shi
Investigational Site Number 392025, Nagoya
Investigational Site Number 392026, Nagoya
Investigational Site Number 392013, Ogawa-Machi, Hikigun
Investigational Site Number 392014, Ohta-Ku
Investigational Site Number 392022, Okawa-Shi
Investigational Site Number 392021, Osaka
Investigational Site Number 392028, Osaka
Investigational Site Number 392029, Osaka
Investigational Site Number 392030, Sapporo
Investigational Site Number 392018, Sendai
Investigational Site Number 392001, Shinjuku-Ku
Investigational Site Number 392020, Suita-Shi
Investigational Site Number 392017, Toshima-Ku
Investigational Site Number 392027, Toyonaka-Shi
Investigational Site Number 392016, Yokohama
Investigational Site Number 392019, Yokohama
Lead Sponsor
Sanofi
INDUSTRY