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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

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

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

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.
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Phase I and Pharmacokinetic Study of the Oral Farnesyl Transferase Inhibitor SCH 66336 Given Twice Daily to Patients With Advanced Solid Tumors

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.