Command Palette

Search for a command to run...

Clinical Trials · NCT02970942

Investigation of Efficacy and Safety of Three Dose Levels of Subcutaneous Semaglutide Once Daily Versus Placebo in Subjects With Non-alcoholic Steatohepatitis.

CompletedPhase 2Semaglutide (Approved)
Phase
Phase 2
Recruitment status
Completed
Sponsor
Novo Nordisk A/S
Enrollment
320
Start date
Nov 2016
Locations
158 sites, 17 countries
Primary endpoint
Percentage of Participants With Non- Alcoholic Steatohepatitis (NASH) Resolution Without Worsening of Fibrosis After 72 Weeks (Yes/No)
View Semaglutide compound reference