A Practical Guide to Drug Development in Academia -

A Practical Guide to Drug Development in Academia

The SPARK Approach
Buch | Softcover
XII, 176 Seiten
2013 | 2014
Springer International Publishing (Verlag)
978-3-319-02200-0 (ISBN)
69,54 inkl. MwSt
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"A lot of hard-won knowledge is laid out here in a brief but informative way. Every topic is well referenced, with citations from both the primary literature and relevant resources from the internet." Review from Nature Chemical Biology

Written by the founders of the SPARK program at Stanford University, this book is a practical guide designed for professors, students and clinicians at academic research institutions who are interested in learning more about the drug development process and how to help their discoveries become the novel drugs of the future. Often many potentially transformative basic science discoveries are not pursued because they are deemed 'too early' to attract industry interest. There are simple, relatively cost-effective things that academic researchers can do to advance their findings to the point that they can be tested in the clinic or attract more industry interest. Each chapter broadly discusses an important topic in drug development, from preclinical work in assay design through clinical trial design, regulatory issues and marketing assessments. After the practical overview provided here, the reader is encouraged to consult more detailed texts on specific topics of interest.

"I would actually welcome it if this book's intended audience were broadened even more. Younger scientists starting out in the drug industry would benefit from reading it and getting some early exposure to parts of the process that they'll eventually have to understand. Journalists covering the industry (especially the small startup companies) will find this book a good reality check for many an over-hopeful press release. Even advanced investors who might want to know what really happens in the labs will find information here that might otherwise be difficult to track down in such a concentrated form."

Daria Mochly-Rosen, Ph.D., is the George D. Smith Professor of Translational Medicine, the Senior Associate Dean for Research, and a Professor in the Department of Chemical and Systems Biology at Stanford University School of Medicine and the Co-director of SPARK. She received her Ph.D. from the Weizmann Institute of Science in Israel, and was a postdoctoral fellow in the department of biochemistry at UC Berkeley. She joined Stanford University in 1993 and served as the chair of her department for four years. In 2003, her lab’s basic research led to the founding of KAI Pharmaceuticals, where she served as the CSO for one year, and as the chair of the Scientific Advisory Committee and a member of the Board of Directors after her return to academia. She also founded ALDEA Pharmaceuticals in 2011. In addition, Dr. Mochly-Rosen served on a variety of review groups including the Peer Review Advisory Committee of the NIH and on the Council of Councils of the NIH.  Kevin Grimes, M.D., M.B.A., received his M.D. from Brown University and his M.B.A. from Stanford University. After his training, he joined the Stanford faculty as an academic internist. He later worked in the medical device and biotechnology sectors before returning to academia. He is currently the Co-director of the SPARK Translational Research Program and Associate Professor of Chemical and Systems Biology at Stanford, where he also teaches drug discovery and development and the practice of internal medicine.

Chapter 1: Getting Started

1.1 Advancing New Treatments to the Clinic within Academia

Daria Mochly-Rosen

1.2 Overview of Drug Discovery and Development

Kevin Grimes

1.3 Assessing Clinical Need

Kevin Grimes

1.4 Target Product Profile (TPP)

Robert Lum

1.5 Project Management and Project Planning

Rebecca Begeley and Daria Mochly-Rosen

Chapter 2: Discovery and Preclinical Work

2.1 Robustness of Preclinical Studies

Daria Mochly-Rosen

2.2 Repurposing Drugs

Kevin Grimes

2.3 Developing Assays for High Throughput Screening (HTS)

Bruce Koch

2.4 Medicinal Chemistry and Lead Optimization

Daniel A. Erlanson

2.5 Vaccine Development

Harry Greenberg

2.6 When to Begin Animal Studies

Daria Mochly-Rosen

2.7 In vivo pharmacology: Multiple Roles in Drug Discovery

Simeon Taylor

2.8 Pharmacokinetics and ADME Properties

Werner Rubas and Emily Egeler

2.9 Route of Administration and Drug Formulation

Terrence F. Blaschke

2.10 Preclinical Safety Studies

Michael Taylor and Kevin Grimes

Chapter 3: Preparing for the Clinic

3.1 Regulatory Considerations in Product Development

Carol Karp

3.2 Manufacturing and Quality Control

Susan Wade

3.3 Technical Development and Manufacturing of Biological Products

Mark Backer

3.4 Clinical Trial Design

Ted McCluskey

3.5 Overview of Clinical Trials

Ted McCluskey

Chapter 4: Transferring Technology

4.1 Intellectual Property

Judy Mohr

4.2 Working with the University Technology Transfer Office

Katharine Ku

4.3 Avoiding Conflicts of Interest

Emily Egeler

4.4 Working with the University Compliance Office

Jennifer Swanton Brown, Nicholas Gaich, and Steven Alexander

Chapter 5: Commercialization and Entrepreneurship

5.1 Selecting the Market for Your Drug

Lilliane Brunner Halbach

5.2 Commercial Assessments

Julie Papanek

5.3 Making a Compelling Pitch to Potential Investors

Leon Chen

5.4 Venture Capital Funding

Kevin Kinsella

5.5 Not-For-Profit Drug Development

Eugenio L. de Hostos

5.6 Legal Aspects of a Start-up Biotechnology Company

Alan C. Mendelson, Peter E. Boyd, and Christopher M. Reilly

5.7 Founder Preferred Stock

Scott M. Iyama and Stephen J. Venuto

5.8 Plan, Organize, Motivate and Control

John Walker

Chapter 6: Concluding Thoughts

6.1 A Call to Action: Changing How We Pursue Drug Discovery and Development

Steven Schow

Erscheint lt. Verlag 8.11.2013
Reihe/Serie SpringerBriefs in Pharmaceutical Science & Drug Development
Zusatzinfo XII, 176 p. 9 illus., 4 illus. in color.
Verlagsort Cham
Sprache englisch
Maße 155 x 235 mm
Gewicht 300 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Medizin / Pharmazie Pharmazie
Naturwissenschaften Chemie Technische Chemie
Technik
Schlagworte academia • assay design • clinical trial • preclinical
ISBN-10 3-319-02200-8 / 3319022008
ISBN-13 978-3-319-02200-0 / 9783319022000
Zustand Neuware
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