This trial is conducted in Europe and North America. The aim of the trial is to assess disease activity and safety in subjects with moderately to severely active Crohn's disease (CD) when treated with NNC 0142-0000-0002.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
78
A single dose administered subcutaneously (s.c., under the skin)
A single dose administered subcutaneously (s.c., under the skin)
Novo Nordisk Clinical Trial Call Center
Anaheim, California, United States
Change in disease activity assessed by CDAI (Crohn's disease activity index)
Time frame: From baseline to week 4
Number of adverse events (AEs)
Time frame: From baseline to weeks 12 and 24
Immunogenicity of NNC 142-0002
Time frame: At week 24
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Novo Nordisk Clinical Trial Call Center
Lakewood, Colorado, United States
Novo Nordisk Clinical Trial Call Center
Chicago, Illinois, United States
Novo Nordisk Clinical Trial Call Center
Louisville, Kentucky, United States
Novo Nordisk Clinical Trial Call Center
Annapolis, Maryland, United States
Novo Nordisk Clinical Trial Call Center
Chevy Chase, Maryland, United States
Novo Nordisk Clinical Trial Call Center
Towson, Maryland, United States
Novo Nordisk Clinical Trial Call Center
Chesterfield, Michigan, United States
Novo Nordisk Clinical Trial Call Center
Troy, Michigan, United States
Novo Nordisk Clinical Trial Call Center
New York, New York, United States
...and 13 more locations