120
Participants
Start Date
July 15, 2021
Primary Completion Date
December 6, 2022
Study Completion Date
January 30, 2023
Semaglutide 2.4 mg and NNC0165-1875 2.0 mg
NNC0165-1875 will be co-escalated once-weekly subcutaneously with semaglutide every 2 weeks for the first 4 weeks, and every 4 weeks for the next 8 weeks until final target dose levels are reached.
Semaglutide 2.4 mg and placebo 2.0 mg
NNC0165-1875 placebo will be co-escalated subcutaneously once-weekly with semaglutide every 2 weeks for the first 4 weeks, and every 4 weeks for the next 8 weeks until final target dose levels are reached.
Semaglutide 2.4 mg and NNC0165-1875 1.0 mg
NNC0165-1875 will be co-escalated subcutaneously once-weekly with semaglutide every 2 weeks for the first 4 weeks, and every 4 weeks for the next 8 weeks until final target dose levels are reached.
Semaglutide 2.4 mg and placebo 1.0 mg
NNC0165-1875 placebo will be co-escalated subcutaneously once-weekly with semaglutide every 2 weeks for the first 4 weeks, and every 4 weeks for the next 8 weeks until final target dose levels are reached.
National Clin Res Inc., Richmond
Health Res of Hampton Roads, Newport News
Accellacare, Wilmington
Coastal Carolina Res Ctr., North Charleston
Medical Uni of SC Charleston, Charleston
Endo Res Solutions Inc, Roswell
Jacksonville Ctr For Clin Res, Jacksonville
L-MARC Research Center, Louisville
Evanston Premier Hlthcr Res, Skokie
Altasciences Clinical Kansas, Inc., Overland Park
Soltero Cardiovascular Research Center, Dallas
Chrysalis Clinical Research, St. George
Diablo Clinical Research, Inc., Walnut Creek
East West Med Res Inst, Honolulu
Lead Sponsor
Novo Nordisk A/S
INDUSTRY