Research Topics
| J F PaoliniSummaryAffiliation: Merck Research Laboratories Country: USA Publications
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Detail Information
Publications
Effects of laropiprant on nicotinic acid-induced flushing in patients with dyslipidemiaJohn F Paolini
Merck Research Laboratories, Rahway, NJ, USA
Am J Cardiol 101:625-30. 2008..LRPT plus ERN was well tolerated. In conclusion, the significant reduction in ERN-induced flushing provided by LRPT plus ERN supports an accelerated ERN dose-advancement paradigm to achieve rapidly a 2-g dose in dyslipidemic patients...
Extended-release niacin/laropiprant: reducing niacin-induced flushing to better realize the benefit of niacin in improving cardiovascular risk factorsJohn F Paolini
Merck and Company, Incorporated, 126 East Lincoln Avenue, Rahway, NJ 07065, USA
Cardiol Clin 26:547-60. 2008..ER niacin/laropiprant generally is tolerated well and represents a new treatment option for dyslipidemia that offers the potential for more patients to receive the lipid-modifying and cardiovascular benefits of niacin...
Measuring flushing symptoms with extended-release niacin using the flushing symptom questionnaire: results from a randomised placebo-controlled clinical trialJ F Paolini
Merck Research Laboratories, Rahway, NJ 07065, USA
Int J Clin Pract 62:896-904. 2008..We developed the Flushing Symptom Questionnaire((c)) (FSQ), a quantitative tool to assess patient-reported flushing, and assessed its ability to characterise ER niacin-induced flushing...
Lipid-modifying efficacy and tolerability of extended-release niacin/laropiprant in patients with primary hypercholesterolaemia or mixed dyslipidaemiaD Maccubbin
Merck Research Laboratories, Rahway, NJ 07065, USA
Int J Clin Pract 62:1959-70. 2008..Laropiprant (LRPT), a PGD(2) receptor (DP1) antagonist that reduces niacin-induced flushing has been combined with extended-release niacin (ERN) into a fixed-dose tablet...
Efficacy and safety of extended-release niacin/laropiprant plus statin vs. doubling the dose of statin in patients with primary hypercholesterolaemia or mixed dyslipidaemiaS Shah
Merck Research Laboratories, Cardiovascular Disease, Merck, Sharp and Dohme Corp, Rahway, NJ 07065, USA
Int J Clin Pract 64:727-38. 2010....
A comparison of the pharmacokinetics of two different formulations of extended-release niacinB Lauring
Merck and Co, Inc, Rahway, NJ 07065 0900, USA
Curr Med Res Opin 25:15-22. 2009..The objective of this study was to compare pharmacokinetic parameters of niacin extended-release tablets (NER uncoated) and niacin extended-release caplet formation (NER coated)...
Validation of a questionnaire to assess niacin-induced cutaneous flushingJosephine M Norquist
Merck Research Laboratories, Department of Epidemiology, North Wales, PA 19454 2505, USA
Curr Med Res Opin 23:1549-60. 2007..To further characterize flushing, a patient-reported Flushing Symptom Questionnaire (FSQ) was developed and validated...
Flushing profile of extended-release niacin/laropiprant versus gradually titrated niacin extended-release in patients with dyslipidemia with and without ischemic cardiovascular diseaseDarbie Maccubbin
Merck Research Laboratories, Rahway, NJ, USA
Am J Cardiol 104:74-81. 2009..In conclusion, improvement in flushing with ERN/LRPT versus gradually titrated N-ER supports a rapidly advanced 1-g --> 2-g dosing regimen, allowing patients to start at 1 g and quickly reach and tolerate the optimal 2 g dose of ERN...
Flushing profile of extended-release niacin/laropiprant at initiation of therapy in Asian lipid clinic patientsDebra Kush
Merck Research Laboratories, Rahway, NJ 07065, USA
Cardiology 114:192-8. 2009..This study compared flushing with a combination tablet of extended-release (ER) niacin (ERN)/LRPT to niacin ER (N-ER; without LRPT) during the first week of therapy among patients in Asia...
Bioequivalence of an ezetimibe/simvastatin combination tablet and coadministration of ezetimibe and simvastatin as separate tablets in healthy subjectsE M Migoya
Merck Research Laboratories, Rahway, NJ 07065 0900, USA
Int J Clin Pharmacol Ther 44:83-92. 2006..To assess the bioequivalence of an ezetimibe/simvastatin (EZE/SIMVA) combination tablet compared to the coadministration of ezetimibe and simvastatin as separate tablets (EZE + SIMVA)...
Simvastatin does not have a clinically significant pharmacokinetic interaction with fenofibrate in humansArthur J Bergman
Merck Research Laboratories, WP75-100, Sumneytown Pike, West Point, PA 19486, USA
J Clin Pharmacol 44:1054-62. 2004..70, 1.43), no clinically significant pharmacokinetic drug interaction between fenofibrate and simvastatin was concluded in humans. The coadministration of simvastatin and fenofibrate in this study was well tolerated...
Effects of ezetimibe on cyclosporine pharmacokinetics in healthy subjectsArthur J Bergman
Merck Research Laboratories, West Point, PA 19486, USA
J Clin Pharmacol 46:321-7. 2006..CyA concentrations should be monitored in patients receiving EZE and CyA...
