This trial is conducted in Europe. The aim of the trial is to evaluate the optimal dosing conditions for GLP-1 analogue NNC0113-0987 when administered orally in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
122
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.
Unnamed facility
Harrow, United Kingdom
Area under the NNC0113-0987 plasma concentration time curve
Time frame: From time 0 to 24 hours after the 10th dosing
Maximum observed NNC0113-0987 plasma concentration
Time frame: 0 to 24 hours after the 10th dosing
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