Trial Profile

A Randomized, Single-Center, Open-Label, Single-dose, 4-Period, 2-Sequence, Fully Replicate Crossover Study To Assess The Bioequivalence Of A Test Fixed Dose Combination Product Versus The Co-Administered Individual Reference Products Containing Bempedoic Acid 180 mg, Ezetimibe 10 mg And Rosuvastatin 20 mg In Healthy Participants

Status: Not yet recruiting

Phase of Trial: Phase I

Latest Information Update: 13 Oct 2025

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At a glance

Drugs Bempedoic acid/ezetimibe/rosuvastatin (Primary) ; Bempedoic acid; Ezetimibe; Rosuvastatin
Indications Dyslipidaemias
Focus Pharmacokinetics
Sponsors Daiichi Sankyo Company

29 Sep 2025 Planned End Date changed from 25 Nov 2025 to 18 Nov 2025.
29 Sep 2025 Planned primary completion date changed from 25 Nov 2025 to 18 Nov 2025.
22 Sep 2025 New trial record

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