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Clinical Trials · NCT02210871

Investigating the Pharmacokinetics, Safety and Tolerability After a Single Subcutaneous Injection of Semaglutide in Subjects With Mild, Moderate or Severe Hepatic Impairment Compared to Subjects With Normal Hepatic Function

CompletedPhase 1Semaglutide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Novo Nordisk A/S
Enrollment
44
Start date
Aug 2014
Locations
4 sites, Poland, Slovakia
Primary endpoint
Area under the semaglutide plasma concentration-time curve
View Semaglutide compound reference