The primary objective of the study is to assess pharmacokinetics, dynamics, safety and tolerability of CiVi007 following single and multiple subcutaneous doses in subjects, including those on statin therapy
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
36
Leeds Clinic
Leeds, West Yorkshire, United Kingdom
LDL Cholesterol
% LDL-C reduction
Time frame: Maximum post dose within 8 weeks
Peak Plasma Concentration (Cmax) of CiVi007
Pharmacokinetic Outcome Measure
Time frame: 8 weeks
PCSK9 level
maximal % reduction in the level of circulating PCSK9
Time frame: Maximum post dose within 8 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.