The primary objective of this study is to evaluate the efficacy of different doses of TA-8995, a cholesteryl ester transfer protein (CETP) inhibitor, on the elevation of high-density lipoprotein cholesterol (HDL-C) and reduction of low-density lipoprotein cholesterol (LDL-C), alone and in combination with statin therapy. The secondary objectives of this study are to determine the safety and tolerability of TA-8995 in patients with mild dyslipidaemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
364
H:S Amager Hospital
Copenhagen, Denmark
Sydvestjysk Sygehus
Esbjerg, Denmark
Herlev University Hospital
Herlev, Denmark
The co-primary efficacy endpoints are the percentage changes in both HDL-C and LDL-C levels at Week 12 compared to baseline.
Time frame: 12 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Hvidovre Hospital
Hvidovre, Denmark
Regionshopitalet - Silkeborg
Silkeborg, Denmark
EB FlevoResearch B.V
Almere Stad, Netherlands
Andromed Amsterdam
Amsterdam, Netherlands
Andromed Leiden
Amsterdam, Netherlands
Academic Medical Centre
Amsterdam-Zuidoost, Netherlands
Andromed Breda B.V
Breda, Netherlands
...and 7 more locations