Pharmacokinetic Comparison Between a Fixed-Dose Combination of Atorvastatin/Omega-3-Acid Ethyl Esters and the Corresponding Loose Combination in Healthy Korean Male Subjects

• Published in: Drug design, development and therapy Vol. 18; pp. 395 - 406
• Main Authors: Khwarg, Juyoung, Lee, Soyoung, Jang, In-Jin, Kang, Won-Ho, Lee, Hye Jung, Kim, Kyu Yeon, Jeong, Ki-Sun, Won, Chongho, Choi, Youn Woong, Ha, Dae Chul, Jung, RaeHoon, Han, Min-Gu, Jung, Won Tae, Nam, Kyu-Yeol, Kim, YeSeul, Yu, Kyung-Sang, Oh, Jaeseong
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2024; Dove; Dove Medical Press
• Subjects: Analysis; cardiovascular disease; Dosage and administration; Drug therapy, Combination; Esters; Omega-3 fatty acids; Original Research; pharmacokinetics; Statins; Unsaturated fatty acids; South Korea; pharmacokinetics; cardiovascular disease
• ISSN: 1177-8881; 1177-8881
• DOI: 10.2147/DDDT.S435885

Statins are widely used in combination with omega-3 fatty acids for the treatment of patients with dyslipidemia. The aim of this study was to compare the pharmacokinetic (PK) profiles of atorvastatin and omega-3-acid ethyl esters between fixed-dose combination (FDC) and loose combination in healthy subjects. A randomized, open-label, single-dose, 2-sequence, 2-treatment, 4-period replicated crossover study was performed. Subjects were randomly assigned to one of the 2 sequences and alternately received four FDC soft capsules of atorvastatin/omega-3-acid ethyl esters (10/1000 mg) or a loose combination of atorvastatin tablets (10 mg × 4) and omega-3-acid ethyl ester soft capsules (1000 mg× 4) for four periods, each period accompanied by a high-fat meal. Serial blood samples were collected for PK analysis of atorvastatin, eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA). PK parameters were calculated by a non-compartmental analysis. The geometric mean ratio (GMR) and its 90% confidence interval (CI) of the FDC to the loose combination were calculated to compare PK parameters. A total of 43 subjects completed the study as planned. The GMR (90% CI) of FDC to loose combination for maximum concentration (C ) and area under the time-concentration curve from zero to the last measurable point (AUC ) were 1.0931 (1.0054-1.1883) and 0.9885 (0.9588-1.0192) for atorvastatin, 0.9607 (0.9068-1.0178) and 0.9770 (0.9239-1.0331) for EPA, and 0.9961 (0.9127-1.0871) and 0.9634 (0.8830-1.0512) for DHA, respectively. The intra-subject variability for C and AUC of DHA was 30.8% and 37.5%, respectively, showing high variability. Both the FDC and the loose combination were safe and well tolerated. The FDC of atorvastatin and omega-3-acid ethyl esters showed comparable PK characteristics to the corresponding loose combination, offering a convenient therapeutic option for the treatment of dyslipidemia.