Muutke küpsiste eelistusi

Oral Formulation Roadmap from Early Drug Discovery to Development [Kõva köide]

Edited by
  • Formaat: Hardback, 272 pages, kõrgus x laius x paksus: 239x160x20 mm, kaal: 476 g
  • Ilmumisaeg: 24-Mar-2017
  • Kirjastus: John Wiley & Sons Inc
  • ISBN-10: 1118907337
  • ISBN-13: 9781118907337
Teised raamatud teemal:
  • Formaat: Hardback, 272 pages, kõrgus x laius x paksus: 239x160x20 mm, kaal: 476 g
  • Ilmumisaeg: 24-Mar-2017
  • Kirjastus: John Wiley & Sons Inc
  • ISBN-10: 1118907337
  • ISBN-13: 9781118907337
Teised raamatud teemal:
Detailing formulation approaches by stage of discovery to early development, this book gives a playbook of practical and efficient strategies to formulate drug candidates with the least chance of failing in clinical development.

    Comes from contributing authors with experience developing formulations on the frontlines of the pharmaceutical industry     Focuses on pre (or non-) clinical and early stage development, the phases where most compounds are used in drug research     Features case studies to illustrate practical challenges and solutions in formulation selection     Covers regulatory filing, drug metabolism and physical and chemical properties, toxicology formulation, biopharmaceutics classification system (BCS), screening approaches, early stage clinical formulation development, and outsourcing
List of Contributors
vii
Preface ix
1 Introduction
1(8)
Elizabeth Kwong
2 Lead Identification/Optimization
9(30)
Mei Wong
Mark McAllister
3 Oral Drug Formulation Development in Pharmaceutical Lead Selection Stage
39(50)
Shayne Cox Gad
4 Bridging End of Discovery to Regulatory Filing: Formulations for IND- and Registration-Enabling Nonclinical Studies
89(26)
Evan A. Thackaberry
5 Planning the First Clinical Trials with Clinical Manufacturing Organization (CMO)
115(24)
Elizabeth Kwong
Caroline McGregor
6 Formulation Strategies for High Dose Toxicology Studies: Case Studies
139(26)
Dennis H. Leung
Pierre Daublain
Mengwei Hu
Kung-I Feng
7 Formulation, Analytical, and Regulatory Strategies for First-in-Human Clinical Trials
165(78)
Lorenzo Capretto
Gerard Byrne
Sarah Trenfield
Lee Dowden
Steven Booth
Index 243
Elizabeth Kwong, PhD, retired from Merck & Co., Inc. in 2011, after 23 years of service. She then established her own company, Kwong Eureka Solutions, as a consultant for small start-up companies and specialty drug products. Dr. Kwong is on the Board of Directors for the Canadian Society of Pharmaceutical Scientists and is also an adjunct professor in the Department of Pharmaceutics at the University of Montreal and Department of Chemistry at Concordia University. More recently, Dr. Kwong also co-founded a start-up company, Giiant Pharma, working on delivering a colon specific PDEIV Inhibitor prodrug for the treatment of ulcerative colitis.