14
Participants
Start Date
February 8, 2023
Primary Completion Date
August 12, 2024
Study Completion Date
August 12, 2024
MK-2060
MK-2060 lyophilized powder diluted in normal saline and administered subcutaneously
Placebo
Normal saline administered subcutaneously
Velocity Clinical Research, New Smyrna Beach ( Site 0003), Edgewater
Advanced Pharma CR, LLC ( Site 0006), Miami
Genesis Clinical Research, LLC ( Site 0004), Tampa
Alliance for Multispecialty Research, LLC ( Site 0002), Knoxville
Merck Sharp & Dohme LLC
INDUSTRY