122
Participants
Start Date
March 31, 2014
Primary Completion Date
July 31, 2014
Study Completion Date
July 31, 2014
NNC0113-0987
For oral administration. All subjects will be treated for 10 consecutive days with five days on 5 mg NNC0113-0987 followed by five days on 10 mg NNC0113-0987. Dose escalation is chosen to increase gastrointestinal tolerability.
Harrow
Lead Sponsor
Novo Nordisk A/S
INDUSTRY