Metabolite Safety in Drug Development

Preface xi List of Contributors xiii 1 Introduction: History of Metabolite Safety in Drug Development 1 Dennis A. Smith and Suzanne L. Iverson 1.1 People, Events, and Reaction, 1 1.2 The Rise of Industrial Drug Metabolism, 2 1.3 The Appearance of Mist, 4 1.4 The Journey Triggered by Thalidomide: Would Present Science have Made a Difference?, 5 1.5 Key Events from Thalidomide to Mist, 8 1.6 The Purpose of this Book, 13 References, 14 2 "Mist" and other Metabolite Guidelines in the Context of Industrial Drug Metabolism 17 Gordon J. Dear and Angus N. R. Nedderman 2.1 A Historical Perspective, 17 2.2 The Emergence of the Regulatory Guidance Documents, 23 2.3 Impact of the Guidelines, 30 2.4 Future Directions, 32 References, 37 3 Metabolite Technology: Qualitative and Quantitative 45 Gordon J. Dear and Andrew McEwen 3.1 Introduction, 45 3.2 Clinical Samples, 46 3.3 Preclinical Samples, 48 3.4 Radiolabeled Test Compounds, 51 3.5 Mass Spectrometry, 55 3.6 NMR Spectroscopy, 65 3.7 Accelerator Mass Spectrometry, 72 References, 75 Further Reading, 85 4 In Vitro Methods for Evaluation of Drug Metabolism: Identification of Active and Inactive Metabolites and the Enzymes that Generate them 87 R. Scott Obach, Amit S. Kalgutkar, and Deepak K. Dalvie 4.1 Introduction, 87 4.2 In Vitro Methods for Metabolite Profiling and Identification, 88 4.2.1 In Vitro Systems We Use: Most Complex to Simplest, 88 4.2.2 Criteria for Selecting the Most Appropriate In Vitro System for In Vitro Metabolite Profiling, 92 4.3 Application of In Vitro Methods for Metabolite Profiling in Drug Discovery and Development, 96 4.3.1 In Vitro Metabolite Profiling and Identification in the Early Drug Discovery Stage, 96 4.3.2 In Vitro Metabolite Profiling and Identification in the Late Drug Discovery Stage: Selection of Candidate Compounds for Further Development, 98 4.3.3 In Vitro Metabolite Profiling and Identification in the Drug Development Stage: Support of Candidate Compounds for New Drug Registration, 101 4.4 How Well Do In Vitro Metabolite Profiles Represent In Vivo Metabolite Profiles?, 103 4.5 Pharmacologically Active Metabolites and their Identification, 104 4.5.1 When Is a Metabolite Considered Active?, 104 4.5.2 Experimental Approaches to Reveal Active Metabolites, 106 4.6 Conclusion, 108 References, 108 5 Integrated Reactive Metabolite Strategies 111 J. Gerry Kenna and Richard A. Thompson 5.1 Introduction, 111 5.2 Role of RMs in Toxicity, 114 5.3 Strategies for Predicting, Assessing, and Derisking RM-Mediated Toxicity, 118 5.3.1 Assessing RM Hazard: Awareness/Avoidance, 118 5.3.2 Assessing RM Risk: Covalent Binding and Dose, 122 5.3.3 Integrated Risk Assessments: Integrating RM Assessment and In Vitro Safety Assay Endpoints, 127 5.3.4 Integrated RM Risk Assessments: Future Directions, 129 References, 131 6 Understanding Drug Metabolism in Humans: In Vivo 141 Lars Weidolf and Ian D. Wilson 6.1 Introduction, 141 6.2 Preclinical Animal Studies, 142 6.2.1 Whole-Body Autoradiography and Imaging, 144 6.3 Early Human In Vivo Metabolism Studies, 146 6.3.1 Pre-FTIM Data Acquisition, 147 6.3.2 The First Clinical Studies, 149 6.3.3 Metabolite Exposure Assessment, 150 6.3.4 Exceptions to Regulatory Recommendations, 153 6.3.5 Dealing with DHMs, 153 6.3.6 The Human ADME Study, 156 6.3.7 Early Metabolite Exposure Assessment and Relevance to the Target Patient Population, 159 6.3.8 Summary, 160 6.4 The "What ifs...?", 162 6.5 Sources of Variability in In Vivo Biotransformation Studies: Species, Strain, Age, and Sex Differences, 162 6.6 Extrahepatic Drug Metabolism (Animals and Man), 164 6.7 Nonhuman Metabolism in Humans, 166 6.8 Nonhuman Models of Human In Vivo Metabolism, 167 6.8.1 "Humanized" Transgenic Mice, 168 6.8.2 "Chimeric" Humanized Mice, 169 6.9 Alternatives to Radiolabels, 170 6.10 Conclusions, 171 References, 172 7 Topical Administration and Safety Testing of Metabolites 177 Vibeke Hougaard Sunesen 7.1 Introduction, 177 7.2 Skin Structure and Function of the Epidermal Layer, 178 7.3 Skin Models, 180 7.3.1 In Vivo Studies, 181 7.3.2 Ex Vivo Skin, 182 7.3.3 In Vitro Skin Models, 182 7.4 Metabolic Capacity of Human Skin, 186 7.4.1 Phase 1 Enzymes, 186 7.4.2 Non-CYP Phase 1 Enzymes, 190 7.4.3 Phase 2 Enzymes, 193 7.5 Species Differences in Metabolic Capacity of the Skin, 196 7.6 Metabolic Capacity of Diseased Skin, 197 7.7 Soft Drug Approach, 198 7.7.1 Soft Corticosteroids, 199 7.7.2 PDE4 Inhibitors, 200 7.8 Exposure to Metabolites and Risk of Adverse Events, 202 7.8.1 Drug Interaction Potential, 204 7.8.2 Toxicities and Safety Concerns, 205 References, 206 8 In Silico Modeling of Metabolite Kinetics 213 Lu Gaohua, Howard Burt, Helen Humphries, Amin Rostami-Hodjegan, and Masoud Jamei 8.1 Introduction, 213 8.1.1 Why Do We Need to Model Metabolite PK?, 213 8.1.2 Brief Review of Existing PBPK Models of Metabolites, 214 8.2 Simcyp Approach to Modeling Metabolite PBPK, 215 8.2.1 Parent/Metabolite PBPK Model Structure, 215 8.2.2 Formation/Absorption of the Metabolite, 217 8.2.3 Distribution of Metabolite, 219 8.2.4 Elimination of Metabolite, 222 8.2.5 Interaction of Metabolite, 222 8.3 Model Verifications, 223 8.3.1 Comparison of Prediction versus Observation, 223 8.3.2 What-If Simulation Examples, 223 8.4 Discussion, 230 8.4.1 Role of M&S in Handling Metabolites, 230 8.4.2 How to Deal with Multiple Metabolites, 231 8.4.3 Role of M&S of Metabolites in Regulatory Submissions, 232 8.5 Concluding Remarks, 232 8.5.1 What has been Achieved?, 232 8.5.2 Future Works, 232 Glossary, 233 Superscription, 233 Subscription, 234 References, 234 9 Introduction to Case Studies 239 Suzanne L. Iverson References, 242 10 A Mass Balance and Metabolite Profiling Study of Sonidegib in Healthy Male Subjects Using Microtrace Approach 243 Piet Swart, Frederic Lozac'h, and Markus Zollinger 10.1 Introduction to the Study, 243 10.2 Radioactive Dose Limitations, 245 10.3 Results, 246 10.4 Metabolite Profiling and Identification, 249 Acknowledgments, 258 References, 258 11 Dealing with Reality: When is it Necessary to Qualify and Quantify Metabolites? Some Case Studies 261 Deepak K. Dalvie, R. Scott Obach, and Amit S. Kalgutkar 11.1 Introduction, 261 11.2 Case Study 1, 261 11.3 Case Study 2, 265 11.4 Case Study 3, 268 References, 271 12 The Value of Metabolite Identification and Quantification in Clinical Studies. Some Case Studies Enabling Early Assessment of Safety in Humans: GlaxoSmithKline 275 Jackie Bloomer, Claire Beaumont, Gordon J. Dear, Stephanie North, and Graeme Young 12.1 GW644784: Species-Specific Metabolites, 276 12.2 Danirixin: Assessment of Victim Drug Interaction Risk Using Bile Sampling, 279 12.3 Sitamaquine: Unique, Active, and Possible Genotoxic Metabolites and Human Radiolabel Study Not Feasible, 280 12.4 SB-773812: Concerns Over Long Half-Life Metabolite and Early Employment of Accelerator Mass Spectrometry, 285 12.5 GW766994: Consideration of Steady-State Kinetics and Multiple Analytical Methodologies for an Accurate Assessment of Human Metabolism, 288 References, 290 13 The Importance of Dose- and Time-Dependent Pharmacokinetics During Early Metabolite Safety Assessment in Humans 293 Laurent Leclercq, Marc Bockx, Hilde Bohets, Hans Stieltjes, Vikash Sinah, and Ellen Scheers References, 303 14 Mist and the Future 305 B. Kevin Park and Dennis A. Smith 14.1 Introduction, 305 14.2 Mist and Pharmacology, 306 14.3 Reactive Metabolites, Pharmacology, and Mist, 309 14.4 Implications of Drug Bioactivation and Covalent Binding for Mist, 309 14.5 Drug Bioactivation and Drug Hepatotoxicity, 311 14.6 Drug-Conjugate Formation and Drug Hypersensitivity, 313 14.7 Drug Bioactivation, Conjugate Formation, and Drug Hypersensitivity, 315 14.8 Toward a Mist Strategy for Reactive Metabolites, 317 References, 318 Index 323