48
Participants
Start Date
November 9, 2020
Primary Completion Date
November 26, 2021
Study Completion Date
November 26, 2021
NNC0471-0119
Participants will be randomised to either of five dose levels 0.3, 0.6, 1.2, 2.4 or 3.6 of NNC0471-0119 nanomol per kilogram body weight, which will be administered as a single dose. NNC0471-0119 will be administered subcutaneously (s.c., under the skin) in fasting state.
Fast-acting insulin aspart
Participants will get a fixed dose of 0.2 units of fast-acting insulin aspart (Fiasp®) per kilogram body weight, administered subcutaneously (s.c., under the skin) in fasting state.
Novo Nordisk Investigational Site, Graz
Lead Sponsor
Novo Nordisk A/S
INDUSTRY