Works matching IS 17427835 AND DT 2005 AND VI 96 AND IP 3
Results: 26
Dissolution– Bioequivalence Non-Correlations.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 262, doi. 10.1111/j.1742-7843.2005.pto960324.x
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A Pharmacokinetic-Pharmacodynamic Model for Predicting Tumour Growth Inhibition in Mice: A Useful Tool in Oncology Drug Development.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 265, doi. 10.1111/j.1742-7843.2005.pto960325.x
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Optimizing Drug Regimens in Cancer Chemotherapy.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 269, doi. 10.1111/j.1742-7843.2005.pto960326.x
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Molecular Modelling of Drug Targets: The Past, the Present and the Future.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 151, doi. 10.1111/j.1742-7843.2005.pto960302.x
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Action COST B15: Modelling During Drug Development.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 149, doi. 10.1111/j.1742-7843.2005.pto960301.x
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- Article
In silicoPredictions of Drug Solubility and Permeability: Two Rate-limiting Barriers to Oral Drug Absorption.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 156, doi. 10.1111/j.1742-7843.2005.pto960303.x
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Whichin vitroScreens Guide the Prediction of Oral Absorption and Volume of Distribution?
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 162, doi. 10.1111/j.1742-7843.2005.pto960304.x
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Prediction of Drug Metabolism and Interactions on the Basis ofin vitroInvestigations.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 167, doi. 10.1111/j.1742-7843.2005.pto960305.x
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The Use ofin vitroData in Risk Assessment.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 176, doi. 10.1111/j.1742-7843.2005.pto960306.x
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On the Prediction of the Human Response: A Recycled Mechanistic Pharmacokinetic/Pharmacodynamic Approach.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 182, doi. 10.1111/j.1742-7843.2005.pto960307.x
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Application of Full Physiological Models for Pharmaceutical Drug Candidate Selection and Extrapolation of Pharmacokinetics to Man.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 193, doi. 10.1111/j.1742-7843.2005.pto960308.x
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Modeling and Monte Carlo Simulations in Oral Drug Absorption.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 200, doi. 10.1111/j.1742-7843.2005.pto960309.x
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Pharmacokinetic/Pharmacodynamic Modelling in Oncological Drug Development.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 206, doi. 10.1111/j.1742-7843.2005.pto960310.x
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Mechanism-Based Modeling of Complex Biomedical Systems.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 212, doi. 10.1111/j.1742-7843.2005.pto960311.x
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The Odds that Clinically Unrecognized Poor or Partial Adherence Confuses Population Pharmacokinetic/Pharmacodynamic Analyses.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 225, doi. 10.1111/j.1742-7843.2005.pto960312.x
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Clinical Trial Simulation: A Tool for Understanding Study Failures and Preventing Them.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 228, doi. 10.1111/j.1742-7843.2005.pto960313.x
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Predicting the Outcome of Phase III Trials using Phase II Data: A Case Study of Clinical Trial Simulation in Late Stage Drug Development.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 235, doi. 10.1111/j.1742-7843.2005.pto960314.x
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Internal Exposure of Children by Simulated Acute Inhalation of Volatile Organic Compounds: The Influence of Chemical Properties on the Child/Adult Concentration Ratio.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 242, doi. 10.1111/j.1742-7843.2005.pto960315.x
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Model Systems Based on Experimental Animals for Studies on Drug Metabolism in Man: (Mini)Pig Cytochromes P450 3A29 and 2E1.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 244, doi. 10.1111/j.1742-7843.2005.pto960316.x
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Pupil Reaction: A Valid Sensitive Clinical Biomarker for 5-HT<sub>1A</sub> Compounds.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 246, doi. 10.1111/j.1742-7843.2005.pto960317.x
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Low-Dose Methotrexate Pharmacokinetics and Pharmacodynamics in the Therapy of Severe Psoriasis.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 247, doi. 10.1111/j.1742-7843.2005.pto960318.x
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Expression of MRP2 and MDR1 and Other Hepatic Markers in Hepatocytesin situand WRL 68 Cellsin vitro.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 249, doi. 10.1111/j.1742-7843.2005.pto960319.x
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Predictive Model for Identifying Potential CYP2D6 Inhibitors.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 251, doi. 10.1111/j.1742-7843.2005.pto960320.x
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Non-Standard Correlations:In vitro in vivoCorrelations for Immediate Release Products: Comparison of Different Bioequivalence Experiments.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 259, doi. 10.1111/j.1742-7843.2005.pto9603223.x
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Evaluation of a Physiologically-Based Pharmacokinetic Approach for Simulating the First-Time-In-Animal Study.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 254, doi. 10.1111/j.1742-7843.2005.pto960321.x
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The Effect of Mdr1 Induction on the Pharmacokinetics of Rhodamine 123 in Rats.
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- Basic & Clinical Pharmacology & Toxicology, 2005, v. 96, n. 3, p. 257, doi. 10.1111/j.1742-7843.2005.pto960322.x
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