170
Participants
Start Date
June 30, 2002
Primary Completion Date
November 30, 2003
Study Completion Date
November 30, 2003
biphasic human insulin 30
Administrated s.c. (subcutaneously, under the skin) for 16 weeks in treatment period 1 followed by 16 weeks in treatment period 2
biphasic insulin aspart 30
Administrated s.c. (subcutaneously, under the skin) for 16 weeks in treatment period 1 followed by 16 weeks in treatment period 2
Novo Nordisk Investigational Site, Bolton
Novo Nordisk Investigational Site, Cardiff
Novo Nordisk Investigational Site, Derby
Novo Nordisk Investigational Site, Dundee
Novo Nordisk Investigational Site, Exeter
Novo Nordisk Investigational Site, Galway
Novo Nordisk Investigational Site, Glasgow
Novo Nordisk Investigational Site, Leicester
Novo Nordisk Investigational Site, Liverpool
Novo Nordisk Investigational Site, London
Novo Nordisk Investigational Site, London
Novo Nordisk Investigational Site, Newcastle
Novo Nordisk Investigational Site, Nottingham
Novo Nordisk Investigational Site, Sheffield
Novo Nordisk Investigational Site, Upton
Novo Nordisk Investigational Site, Wirral, Merseyside
Novo Nordisk Investigational Site, York
Lead Sponsor
Novo Nordisk A/S
INDUSTRY