Population Pharmacokinetics of Abrocitinib in Healthy Individuals and Patients with Psoriasis or Atopic Dermatitis
暂无分享,去创建一个
[1] J. Silverberg,et al. Efficacy and Safety of Abrocitinib in Patients With Moderate-to-Severe Atopic Dermatitis , 2020, JAMA dermatology.
[2] J. Bauman,et al. P190 - The effect of CYP2C9 and CYP2C19 genotype on the pharmacokinetics of PF 04965842, A JAK1 inhibitor in clinical development , 2020 .
[3] A. Nader,et al. Pharmacokinetics of Upadacitinib in Healthy Subjects and Subjects With Rheumatoid Arthritis, Crohn's Disease, Ulcerative Colitis, or Atopic Dermatitis: Population Analyses of Phase 1 and 2 Clinical Trials , 2019, Journal of clinical pharmacology.
[4] E. Peeva,et al. Efficacy and Safety of Oral Janus Kinase 1 Inhibitor Abrocitinib for Patients With Atopic Dermatitis , 2019, JAMA dermatology.
[5] S. Tarabar,et al. Evaluation of a Janus kinase 1 inhibitor, PF‐04965842, in healthy subjects: A phase 1, randomized, placebo‐controlled, dose‐escalation study , 2018, British journal of clinical pharmacology.
[6] Z. Draelos,et al. Efficacy and safety of the Janus kinase 1 inhibitor PF‐04965842 in patients with moderate‐to‐severe psoriasis: phase II, randomized, double‐blind, placebo‐controlled study , 2018, The British journal of dermatology.
[7] B. Strober,et al. Pharmacokinetic Characteristics of Tofacitinib in Adult Patients With Moderate to Severe Chronic Plaque Psoriasis , 2018, Clinical pharmacology in drug development.
[8] Mark J. Mitton-Fry,et al. Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases. , 2018, Journal of medicinal chemistry.
[9] A. Othman,et al. Population Pharmacokinetics of Upadacitinib in Healthy Subjects and Subjects with Rheumatoid Arthritis: Analyses of Phase I and II Clinical Trials , 2017, Clinical Pharmacokinetics.
[10] C. Knibbe,et al. Hepatic Drug Metabolism in Pediatric Patients , 2017 .
[11] K. Ueda,et al. Pharmacokinetics and Differential Regulation of Cytochrome P450 Enzymes in Type 1 Allergic Mice , 2016, Drug Metabolism and Disposition.
[12] D. Tibboel,et al. Drug metabolism for the paediatrician , 2014, Archives of Disease in Childhood.
[13] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .
[14] D R Mould,et al. Basic Concepts in Population Modeling, Simulation, and Model-Based Drug Development—Part 2: Introduction to Pharmacokinetic Modeling Methods , 2013, CPT: pharmacometrics & systems pharmacology.
[15] D R Mould,et al. Basic Concepts in Population Modeling, Simulation, and Model-Based Drug Development , 2012, CPT: pharmacometrics & systems pharmacology.
[16] Jonathan L. Kaye,et al. Review of paediatric gastrointestinal physiology data relevant to oral drug delivery , 2011, International Journal of Clinical Pharmacy.
[17] ET Morgan,et al. Impact of Infectious and Inflammatory Disease on Cytochrome P450–Mediated Drug Metabolism and Pharmacokinetics , 2009, Clinical pharmacology and therapeutics.
[18] Julie A. Johnson,et al. Differences in Drug Pharmacokinetics Between East Asians and Caucasians and the Role of Genetic Polymorphisms , 2004, Journal of clinical pharmacology.
[19] Stuart L. Beal,et al. Ways to Fit a PK Model with Some Data Below the Quantification Limit , 2001, Journal of Pharmacokinetics and Pharmacodynamics.