60
Participants
Start Date
February 29, 2016
Primary Completion Date
July 31, 2016
Study Completion Date
July 31, 2016
Cohort 1: bococizumab 150 mg + rHuPH20
bococizumab 150 mg + rHuPH20 administered SC to healthy volunteers
Cohort 2: bococizumab 300 mg
bococizumab 300 mg administered SC to healthy volunteers
Cohort 3: bococizumab 300 mg + rHuPH20
bococizumab 300 mg + rHuPH20 administered SC to healthy volunteers
Cohort 5: bococizumab 450 mg + rHuPH20
bococizumab 450 mg + rHuPH20 administered SC to healthy volunteers
Cohort 4: bococizumab 300 mg + rHuPH20
bococizumab 300 mg + rHuPH20 administered SC to subjects with hypercholesterolemia receiving a statin
Pfizer Clinical Research Unit, Brussels
Lead Sponsor
Collaborators (1)
Halozyme Therapeutics
INDUSTRY
Pfizer
INDUSTRY