92
Participants
Start Date
August 2, 2021
Primary Completion Date
July 7, 2022
Study Completion Date
July 7, 2022
Semaglutide 2.4 mg
Semaglutide administered s.c. (subcutaneously, under the skin) once weekly. Participants will gradually increase the dose until they reach the target dose, and will continue on the this dose once weekly up to 32 weeks
Cagrilintide 2.4 mg
Cagrilintide administered s.c. (subcutaneously, under the skin) once weekly. Participants will gradually increase the dose until they reach the target dose, and will continue on the this dose once weekly up to 32 weeks
Placebo (semaglutide)
"Placebo (semaglutide) administered s.c. (subcutaneously, under the skin) once weekly.~Participants will gradually increase the dose until they reach the target dose, and will continue on the this dose once weekly up to 32 weeks"
Placebo (cagrilintide)
"Placebo (cagrilintide) administered s.c. (subcutaneously, under the skin) once weekly.~Participants will gradually increase the dose until they reach the target dose, and will continue on the this dose once weekly up to 32 weeks"
MD Medical Research, Oxon Hill
PharmQuest Life Sciences LLC, Greensboro
Accellacare, Wilmington
Florida Inst For Clin Res, Orlando
Clinical Trial Research Associates,Inc, Plantation
Uni of Alabama at Birmingham, Birmingham
Holston Medical Group, Kingsport
Plains Clinical Research Center, LLC_Fargo, Fargo
Macoupin Research Group, Gillespie
Velocity Clinical Res-Dallas, Dallas
DCOL Ctr for Clin Res, Longview
PlanIt Research, PLLC, Houston
New West Physicians,Inc., Golden
Velocity Clin Res Los Angeles, Los Angeles
Pacific Clinical Studies, Los Alamitos
Encompass Clinical Research_Spring Valley, Spring Valley
East West Med Res Inst, Honolulu
Capital Clin Res Ctr,LLC, Olympia
Lead Sponsor
Novo Nordisk A/S
INDUSTRY