This trial is conducted in the United States of America. The aim of this trial is to investigate Safety, Tolerability, PK (the exposure of the trial drug in the body) and PD (the effect of the investigated drug on the body) for Multiple Doses of NNC9204-0530 in Combination with Liraglutide in Male and Female Subjects being Overweight or with Obesity
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
187
Once-daily subcutaneous (s.c., under the skin) administration.
Once-daily subcutaneous (s.c., under the skin) administration.
Once-daily subcutaneous (s.c., under the skin) administration
Novo Nordisk Investigational Site
Tempe, Arizona, United States
Novo Nordisk Investigational Site
Lincoln, Nebraska, United States
Number of treatment emergent adverse events
Time frame: Day 1-112
Area under the NNC9204-0530 serum concentration-time curve
Time frame: Day 84-112
Time to maximum serum concentration of NNC9204-0530
Time frame: Day 84-112
Change in HbA1C
Time frame: Day -1, Day 85
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