61
Participants
Start Date
May 10, 2013
Primary Completion Date
September 17, 2013
Study Completion Date
September 17, 2013
MK-8521 35μg
Single dose 35μg subcutaneous (SC) injection in a treatment period (Part 3, Panel H)
MK-8521 100μg
Single dose 100μg SC injection in a treatment period (Part 1, Panel A) and (Part 2, Panel D)
MK-8521 125μg
Single dose 125μg SC injection in a treatment period (Part 2, Panel E) and (Part 3, Panel H)
MK-8521 150μg
Single dose 150μg SC injection in a treatment period (Part 1, Panel B)
MK-8521 175μg
Single dose 175μg SC injection in a treatment period (Part 1, Panel B)
MK-8521 200μg
Single dose MK-8521 200μg SC injection in a treatment period (Part 1, Panel B)
MK-8521 300μg
Single dose 300μg SC injection in a treatment period (Part 1, Panel A)
MK-8521 50/72μg
MK-8521 50μg SC injection Days 1-5 and 72μg Days 6-10 (Part 2, Panel C)
MK-8521 72/125μg
MK-8521 72μg SC injection Days 1-7 and 125μg Days 8-14 (Part 2, Panel F)
MK-8521 100/150μg
MK-8521 100μg SC injection Days 1-5 and 150μg Days 6-10 SC in a treatment period (Part 2, Panel D)
MK-8521 125/150μg
MK-8521 SC 125μg SC injection Days 1-5 and 150μg Days 6-10 (Part 2, Panel E)
Placebo
Placebo to MK-8521 SC injection in a treatment period (Parts 1, 2, and 3)
Merck Sharp & Dohme LLC
INDUSTRY