This trial is conducted in the United States of America (USA). The aim of the trial is to investigate safety, tolerability and pharmacokinetics (the exposure of the trial drug in the body) for single doses of NNC9204-0530 alone and in combination with liraglutide in overweight to obese but otherwise healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
163
Administered as single subcutaneous (s.c., under the skin) injections.
Administered as subcutaneous (s.c., under the skin) injections of 1.8 or 3.0 mg.
Administered as single subcutaneous (s.c., under the skin) injections.
Novo Nordisk Investigational Site
Overland Park, Kansas, United States
Number of treatment emergent adverse events recorded
Time frame: From time of dosing of NNC9204-0530 (Day 1) until completion of the follow-up visit (Day 21-27)
Area under the NNC9204-0530 serum concentration-time curve
Time frame: From dosing visit to infinity calculated on 0-24 days NNC9204-0530 serum concentration-curve based on 21 sampling points
Maximum concentration of NNC9204-0530 in serum
Time frame: From dosing visit to infinity calculated on 0-24 days NNC9204-0530 serum concentration-curve based on 21 sampling points
The time to maximum concentration of NNC9204-0530 in serum
Time frame: From dosing visit to infinity calculated on 0-24 days NNC9204-0530 serum concentration-curve based on 21 sampling points
The terminal half-life of NNC9204-0530
Time frame: From dosing visit to infinity calculated on 0-24 days NNC9204-0530 serum concentration-curve based on 21 sampling points
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