Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Melton B. Affrime"'
Publikováno v:
Pediatric Asthma, Allergy & Immunology. 19:146-153
Current treatment guidelines recommend intranasal corticosteroids or nonsedating antihistamines as first-line therapy for allergic rhinitis (AR). Because of concerns regarding the systemic safety of intranasal corticosteroids in children, the present
Publikováno v:
British Journal of Clinical Pharmacology. 56:131-134
Aims To assess the single-dose pharmacokinetics and tolerability of pegylated interferon-α2b (PEG-Intron) in young and elderly healthy subjects. Methods In this parallel-design study, a single 1 µg kg−1 PEG-Intron dose was given subcutaneously to
Autor:
Samir K. Gupta, Sheila Jacobs, Suzanne K. Swan, Amy L. Pittenger, Melton B. Affrime, Emlyn Tobillo, Thomas Marbury, Vijay Batra, Paul Glue, Marshall Sack
Publikováno v:
The Journal of Clinical Pharmacology. 42:1109-1115
This study evaluates the pharmacokinetics and safety of pegylated interferon-alpha2b (PEG-Intron) following a single-dose subcutaneous injection into subjects with normal renal function, subjects with chronic renal impairment, and patients on hemodia
Autor:
Melton B. Affrime, J. Jen, Paul Glue, Carol Chung, Gerald Hajian, Mark Laughlin, Samuel Heft, Samir K. Gupta
Publikováno v:
Clinical Pharmacology & Therapeutics. 72:349-361
Background Combination therapy of ribavirin with interferon alfa-2b and pegylated interferon alfa-2b is currently approved for the treatment of chronic hepatitis C. Approved ribavirin dosages vary from a fixed dosage of 800 mg/d to as much as 1200 mg
Autor:
Vijay Batra, James E. Patrick, Bo Yang, L. Mellars, Melton B. Affrime, Enrico P. Veltri, Teddy Kosoglou, Yali Zhu, David L. Cutler, Stephen E. Maxwell, Paul Statkevich, Ingo Meyer
Publikováno v:
British Journal of Clinical Pharmacology. 54:309-319
Aims The primary aims of these two single-centre, randomized, evaluator-blind, placebo/positive-controlled, parallel-group studies were to evaluate the potential for pharmacodynamic and pharmacokinetic interaction between ezetimibe 0.25, 1, or 10 mg
Publikováno v:
Clinical Pharmacokinetics. 41:37-44
Objective: This study was performed to assess the electrocardiographic safety and pharmacokinetics of desloratadine in combination with the CYP3A4 inhibitor ketoconazole. Design: A randomised, placebo-controlled, third-party—blind, 2-way crossover
Publikováno v:
Clinical Pharmacokinetics. 41:13-19
Objective: To characterise the pharmacokinetic profile of desloratadine and its main metabolite, 3-hydroxy (3-OH) desloratadine, in a patient population representative of the population studied in the desloratadine clinical efficacy and safety studie
Publikováno v:
Clinical Pharmacokinetics. 41:311-318
Certain foods, such as grapefruit juice, are known to substantially alter the bioavailability of some drugs. These effects may be mediated by interactions with enzyme systems, such as cytochrome P450, or with active transporter systems, such as P-gly
Autor:
Samir K. Gupta, Christopher Banfield, Bhavna Kantesaria, Mark Marino, Melton B. Affrime, Robert P. Clement, Vijay Batra
Publikováno v:
Clinical Therapeutics. 23:451-466
Significant cardiac toxicity has been associated with some older antihistamines (eg, terfenadine and astemizole) when their plasma concentrations are increased. There is thus a need for a thorough assessment of the cardiac safety of newer antihistami
Autor:
Rachel Bacon, Stephen P. Newman, Mark Marino, Melton B. Affrime, G.R. Pitcairn, Peter H. Hirst, Hannah Pickering
Publikováno v:
Clinical Therapeutics. 22:1483-1493
Background: A new inhaled suspension formulation of mometasone furoate (MF), a potent corticosteroid with minimal systemic availability, has been developed for the treatment of asthma. This formulation is delivered by metered-dose inhaler (MDI) using