78
Participants
Start Date
May 8, 2001
Primary Completion Date
March 5, 2003
Study Completion Date
March 5, 2003
somatropin
Injected subcutaneously 7 times per week after reconstitution with liquid buffer prior to use. Dose level of 0.024-0.050 mg/kg at the discretion of the practicing paediatric endocrinologists
somatropin
Injected subcutaneously 7 times per week. Dose level of 0.024-0.050 mg/kg at the discretion of the practicing paediatric endocrinologists
Novo Nordisk Investigational Site, Manhasset
Novo Nordisk Investigational Site, Pittsburgh
Novo Nordisk Investigational Site, Pittsburgh
Novo Nordisk Investigational Site, Hershey
Novo Nordisk Investigational Site, Wilmington
Novo Nordisk Investigational Site, Washington D.C.
Novo Nordisk Investigational Site, Atlanta
Novo Nordisk Investigational Site, Gainesville
Novo Nordisk Investigational Site, Miami
Novo Nordisk Investigational Site, Tampa
Novo Nordisk Investigational Site, Louisville
Novo Nordisk Investigational Site, Chicago
Novo Nordisk Investigational Site, Chicago
Novo Nordisk Investigational Site, Wichita
Novo Nordisk Investigational Site, Los Angeles
Novo Nordisk Investigational Site, Seattle
Novo Nordisk Investigational Site, Los Angeles
Novo Nordisk Investigational Site, Orlando
Novo Nordisk Investigational Site, Lexington
Novo Nordisk Investigational Site, Worcester
Novo Nordisk Investigational Site, Akron
Lead Sponsor
Novo Nordisk A/S
INDUSTRY