Early Phase Drug Evaluation in ManJohn O'Grady, Otto I Linet CRC Press, 2020 M02 3 - 737 pages Early Phase Drug Evaluation in Man is a comprehensive, practical guide that covers pre-clinical information relevant to early human studies, including pharmaceutical, metabolic, toxicological, and regulatory aspects, as well as the general considerations relevant to all early human studies. Each major therapeutic area is considered by class of activity of drug. The chapters describe what measurements of drug activity are available in healthy human subjects and in patients, how to make the measurements, their value and their limitations. The contributors have been drawn internationally from the pharmaceutical industry and academia. Early Phase Drug Evaluation in Man will provide an important reference guide for industry and academic professionals involved in the development of new drugs. |
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Page 6
... DOSAGE FORM CONSIDERATIONS A review of pharmaceutical dosage forms available in most major markets around the globe would indicate that tablets and capsules are by far the most widely used dosage form , primarily because of advances in ...
... DOSAGE FORM CONSIDERATIONS A review of pharmaceutical dosage forms available in most major markets around the globe would indicate that tablets and capsules are by far the most widely used dosage form , primarily because of advances in ...
Page 12
... dose for therapeutic dose may suffice , but inadequate bioavailabil- ity may result for a drug with similar solubility which requires a therapeutic dose of several hundred milligrams . Similarly , a highly lipophilic drug may have low ...
... dose for therapeutic dose may suffice , but inadequate bioavailabil- ity may result for a drug with similar solubility which requires a therapeutic dose of several hundred milligrams . Similarly , a highly lipophilic drug may have low ...
Page 26
... dose situation . High dose exposure may also lead to non - linear pharmacokinetics ( i.e. AUC does not increase in proportion to drug dose ) , which may result in prolonged exposure and bioaccumulation in test species . The use of high ...
... dose situation . High dose exposure may also lead to non - linear pharmacokinetics ( i.e. AUC does not increase in proportion to drug dose ) , which may result in prolonged exposure and bioaccumulation in test species . The use of high ...
Page 31
... dose ( approximately 90 % ) being delivered orally . The intraperitoneal route is frequently used in animal studies on the basis of the assumption , which is not always valid ( Pang , 1983 ) , that the entire dose will be absorbed into ...
... dose ( approximately 90 % ) being delivered orally . The intraperitoneal route is frequently used in animal studies on the basis of the assumption , which is not always valid ( Pang , 1983 ) , that the entire dose will be absorbed into ...
Page 32
... dosage levels that are repre- sentative of the doses used in pharmacology and subchronic toxicity studies . These studies are also conducted in other species used in the toxicological evaluation of the drug . Human radiotracer studies ...
... dosage levels that are repre- sentative of the doses used in pharmacology and subchronic toxicity studies . These studies are also conducted in other species used in the toxicological evaluation of the drug . Human radiotracer studies ...
Contents
Organisation and Decision Making | 97 |
Ethical and Legal Considerations | 137 |
Measuring Drug Activity in Man | 193 |
Assessment of Drug Effects on the Cardiovascular System ... | 251 |
Assessment of Drug Effects on the Respiratory System ... | 349 |
Assessment of Drug Effects on the Central Nervous System ... | 377 |
Assessment of Drug Effects on the Gastrointestinal System ... | 455 |
Assessment of Drug Effects on the Kidney | 493 |
Assessment of the Effects of Drugs Used in Obstetrics and Gynaecology ... | 519 |
Assessment of Drug Activity in the Skin | 551 |
Assessment of Drugs Used for the Treatment of Metabolic Disorders ... | 599 |
Assessment of the Effects of Chemotherapeutic Agents ... | 625 |
Assessment of Drugs Affecting the Inflammatory Process and Pain ... | 655 |
Index | 703 |
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absorption acid action activity acute administration adverse agents analgesic animal antidepressant anxiety anxiolytic assay assessment asthma benzodiazepines bioavailability biological blood pressure cardiac output cells changes chronic Clin clinical research clinical trials compound concentration consent coronary corticosteroids determine disease diuretics dosage dose drug development duration eczema effects of drugs efficacy enantiomers enzyme ethics committee evaluation excretion exercise experimental factors function gastric gastrointestinal gastrointestinal tract glucose guidelines healthy volunteers heart human important increase induced inhibition insulin intravenous investigator laboratory levels measurement metabolism metabolites method minoxidil monitoring myocardial normal NSAIDs oral pain parameters patients performed Pharm pharmaceutical pharmacodynamic pharmacokinetic pharmacological placebo plasma platelet potential preclinical predictive produce prostaglandin protocol receptor regulatory renal response rheumatoid arthritis risk safety scales Shuster side-effects skin specific studies subjects symptoms techniques therapeutic therapy tion tolerance toxicology treatment urine uterine visual analogue scales vitro vivo