This trial is conducted in the United States of America. The aim of the trial is to investigate Safety, Tolerability, PK and PD for Multiple Doses of NNC9204-0530 in Male and Female Subjects being overweight or with obesity
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
48
Administered daily subcutaneously (s.c., under the skin)
Administered daily subcutaneously (s.c., under the skin)
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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