D
David L. Cutler
Researcher at Merck & Co.
Publications - 86
Citations - 2762
David L. Cutler is an academic researcher from Merck & Co.. The author has contributed to research in topics: Vorapaxar & Pharmacokinetics. The author has an hindex of 23, co-authored 84 publications receiving 2615 citations. Previous affiliations of David L. Cutler include University of Amsterdam & Schering-Plough.
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SCH 503034, a Novel Hepatitis C Virus Protease Inhibitor, Plus Pegylated Interferon α-2b for Genotype 1 Nonresponders
Christoph Sarrazin,Christoph Sarrazin,Regine Rouzier,Frank Wagner,Nicole Forestier,Nicole Forestier,Dominique Larrey,Samir K. Gupta,Musaddeq Hussain,Amrik Shah,David L. Cutler,Jenny Zhang,Stefan Zeuzem,Stefan Zeuzem +13 more
TL;DR: Combination therapy with SCH 503034 and PEG-IFN-alpha-2b was well tolerated, with no clinically significant changes in safety parameters, and preliminary results of antiviral activity of the combination suggest a potential new therapeutic option for this hard-to-treat, nonresponder patient population.
Journal Article
A Phase I Trial of the Farnesyl Transferase Inhibitor SCH66336: Evidence for Biological and Clinical Activity
Alex A. Adjei,Charles Erlichman,Jenny N. Davis,David L. Cutler,Jeff A. Sloan,Randolph S. Marks,Lorelei J. Hanson,Phyllis A. Svingen,Pamela J. Atherton,W. Robert Bishop,Paul Kirschmeier,Scott H. Kaufmann +11 more
TL;DR: This study establishes the dose for future testing on this schedule and provides the first evidence of successful inhibition of FT in the clinical setting and the first hint of clinical activity for this class of agents.
Journal Article
Absorption, Metabolism, and Excretion of 14C-Temozolomide following Oral Administration to Patients with Advanced Cancer
Sharyn D. Baker,Sharyn D. Baker,Mark A. Wirth,Paul Statkevich,Pascale Reidenberg,Kevin B. Alton,S E Sartorius,Margaret Dugan,David L. Cutler,Vijay Batra,Louise B. Grochow,Ross C. Donehower,Eric K. Rowinsky +12 more
TL;DR: A first- order absorption, one-compartment linear model, which included first-order formation ofMTIC from TMZ and elimination of MTIC via degradation to AIC, and a peripheral distribution compartment for AIC adequately described the plasma TMZ, MTIC,and AIC concentrations, demonstrated rapid oral absorption and high systemic availability.
Journal ArticleDOI
Interleukin-10 Inhibits Activation of Coagulation and Fibrinolysis During Human Endotoxemia
Dasja Pajkrt,Dasja Pajkrt,Tom van der Poll,Tom van der Poll,M. Levi,M. Levi,David L. Cutler,David L. Cutler,Melton B. Affrime,Melton B. Affrime,Abraham E. van den Ende,Abraham E. van den Ende,Jan Wouter ten Cate,Jan Wouter ten Cate,Sander J. H. van Deventer,Sander J. H. van Deventer +15 more
TL;DR: In this article, the effects of recombinant human IL-10 on LPS-induced activation of the hemostatic mechanisms in vivo were investigated in a cross-over study of human endotoxemia.
Journal ArticleDOI
Phase I and Pharmacokinetic Study of the Oral Farnesyl Transferase Inhibitor SCH 66336 Given Twice Daily to Patients With Advanced Solid Tumors
Ferry A.L.M. Eskens,Ahmad Awada,David L. Cutler,Maja J.A. de Jonge,Gré P.M. Luyten,Marije N. Faber,Paul Statkevich,Alex Sparreboom,Jaap Verweij,Axel-R. Hanauske,Martine Piccart +10 more
TL;DR: Plasma and urine pharmacokinetic analysis showed a greater than dose-proportional increase in drug exposure and peak plasma concentrations, with increased parameters at day 15 compared with day 1, indicating some accumulation on multiple dosing.