The design of this study will enable an extensive evaluation of safety, tolerability, and PK-PD relationship following 4 weeks of dosing in patients with Coronary heart Disease
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
104
Pinnacle Research Group
Anniston, Alabama, United States
Novartis Investigative Site
Philadelphia, Pennsylvania, United States
Icon Clinical Research
San Antonio, Texas, United States
Novartis Investigator Site
Safety and tolerability of APL180
Time frame: Throughout the study
Pharmacokinetics of APL180
Time frame: Throughout the study
Evaluate effects of APL180 biomarkers
Time frame: Throughout the study
Pharmacokinetic-pharmacodynamic relationship of APL180
Time frame: Throughout the study
Effect of APL180 on exploratory biomarkers,
Time frame: Throughout the study
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Copenhagen, Denmark
Novartis Investigator Site
Mainz, Germany
Novartis Investigator Site
Mannheim, Germany
Novartis Investigator Site
Neuss, Germany
Novartis Investigator Site
Rehovot, Israel
Novartis Investigator Site
Tel Aviv, Israel
Novartis Investigator Site
Zrifin, Israel
...and 1 more locations