611
Participants
Start Date
October 31, 2008
Primary Completion Date
January 31, 2011
Study Completion Date
January 31, 2011
biphasic insulin aspart 30
Start dose and frequency and safety data collection at the discretion of the physician following clinical practice
biphasic insulin aspart 50
Start dose and frequency and safety data collection at the discretion of the physician following clinical practice
biphasic insulin aspart 70
Start dose and frequency and safety data collection at the discretion of the physician following clinical practice
Novo Nordisk Investigational Site, Brussels
Novo Nordisk Investigational Site, Luxembourg
Lead Sponsor
Novo Nordisk A/S
INDUSTRY