32
Participants
Start Date
November 30, 2009
Primary Completion Date
May 31, 2010
Study Completion Date
May 31, 2010
insulin degludec
Single dose of 0.4 U/kg body weight injected s.c. (under the skin) in subjects with end stage renal disease
insulin degludec
Single dose of 0.4 U/kg body weight injected s.c. (under the skin) in subjects with mild renal impairment
insulin degludec
Single dose of 0.4 U/kg body weight injected s.c. (under the skin) in subjects with moderate renal impairment
insulin degludec
Single dose of 0.4 U/kg body weight injected s.c. (under the skin) in healthy volunteers
insulin degludec
Single dose of 0.4 U/kg body weight injected s.c. (under the skin) in subjects with severe renal impairment
Novo Nordisk Investigational Site, Budapest
Lead Sponsor
Novo Nordisk A/S
INDUSTRY