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产业会议汇总历

TIDES: Oligonucleotide and Peptide® Research, Technology and Product Development

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The Industry's Only Event for Full Coverage of the Oligonucleotide and Peptide Markets

2012年5月20-23日· Mandalay Bay Resort & Casino · Las Vegas, NV

会前研讨会讲习 · 星期日

会前研讨会讲习 · 星期日

会前研讨会讲习 · 星期日, 2012年5月20日

8:30
Registration and Coffee

Course 1

Business and Operational Strategies for Successful Oligonucleotide Development

9:00 am – 3:30 pm

Course Leaders:
G. Susan Srivatsa, Ph.D., President, ElixinPharma
Fran Wincott, Ph.D., President, Wincott and Associates, LLC

Chemical, pharmaceutical and analytical development of oligonucleotides continues to be challenging due to the increased complexities of development programs and an evolving regulatory landscape. As contract organizations are a major part of most development efforts, it is becoming increasingly important to consider business issues such as intellectual property, know how, confidentiality and other factors when choosing a manufacturing partner as these factors impact downstream development such as site/process changes; business development; licensing, etc. This workshop will present strategies and case studies for managing the business aspects of process and analytical development for commercial and regulatory success.

Management of Intellectual Property and Know-How Challenges for Manufacturing and Commercial Success: Who Owns what and Why?
James A. Powell, President, Meridian Consulting Services, Inc.

Strategies for Management of Process Development and Manufacturing during Early Stage Development: Rent, Buy or DIY?
Fran Wincott, Ph.D., President, Wincott and Associates, LLC

Case
Study
Use of Current Best Practices for Manufacturing a DNA Duplex
Scott Harris, VP Regulatory Affairs and Product Development, Adynxx

Case
Study
Combination of Existing and Customized Approaches for Manufacturing PEGylated Spiegelmers
Stefan Vonhoff, Ph.D., VP CMC, Noxxon Pharma AG, Germany

Strategies for Management of Analytical Development and Quality Control during Early Stage Development: Rent, Buy or DIY?
G. Susan Srivatsa, Ph.D., President, ElixinPharma

Case
Study
Customized Method Development and Transfer to Support Clinical Development of an Oligonucleotide
Presenter to be announced

Course 2

Peptide Manufacturing and Analysis: A Basic Tutorial

9:00 am – 3:30 pm

Course Leaders:
Firoz D. Antia, Ph.D., Executive Director, Product Development, Palatin Technologies, Inc.
Aleksander Swietlow, Ph.D., Principal Scientist, Amgen Inc.

Hear in-depth presentations on what you need to know about chemical, analytical and pharmaceutical development of peptides as you develop your peptide therapeutic. Topics covered will include updates on the latest synthesis technologies and analytical methods. Learn also about the latest in regulatory trends including the new process validation guidance. Participate in an interactive discussion to ask your questions to the experts.

Course Introduction
Aleksander Swietlow, Ph.D., Principal Scientist, Amgen Inc.

New, Unpublished Data

Large Scale Peptide API Manufacturing: Latest Development in Chemistry and Technology
Guenther Loidl, Ph.D., Vice President, R&D, Bachem AG, Switzerland

Case
Study
Peptide Manufacturing Strategies: Key Technical, Regulatory, Environmental and Economic Considerations
Mimoun Ayoub, Ph.D., Vice President, Global Business, Sales and Strategic Developments, Peptisyntha S.A., Member of the Solvay Group, Belgium

Manufacturing Considerations for Conjugates
Olivier Laurent, Ph.D., Director, Protein Science, Pfizer Biotherapeutics R&D - CovX

Points to Consider in Developing Analytical Methods for Peptide Therapeutics
Aleksander Swietlow, Ph.D., Principal Scientist, Amgen Inc.

Afternoon Chairperson: Firoz D. Antia, Ph.D., Executive Director, Product Development, Palatin Technologies, Inc.

Taking a Peptide to Initial IND -What Analytical Info Do You Need?
Achim Schultze, Associate Director, Pharmaceutical Analysis, Palatin Technologies, Inc.

Case
Study
Incorporation of the New FDA Guideline on Process Validation - A Peptide API Case Study
Jens Finnman, Process Validation Specialist, PolyPeptide Laboratories AB, Sweden

Managing CMC Development to Support Regulatory Submissions
Peter Larsson, Director, Regulatory Affairs, PolyPeptide Laboratories, Inc.

Course 3

Early Drug Product Development

9:00 am – 1:00 pm

Course Leader:
Gregory E. Hardee, Senior Pharmaceutical Consultant, OligoDevelopment.com

This course will cover the essential subject matter required to quickly and efficiently move a discovery candidate into the clinic. Specific examples to be discussed will address the realities of short timelines, limited drug supply and technological peculiarities. Additionally, attention will be given to the goals for three very different formulations: toxicology; clinical proof-of-concept; and efficiency improvements.

  1. What is the goal of formulation?
  2. Toxicology formulation considerations
  3. Pre-formulation studies (pilot formulations)
  4. Formulation development: parenteral
  5. Formulation development: non-parenteral
  6. Supporting analytical strategy
  7. Evolution of the drug product specification
  8. Clinical batch considerations - production, supply chain, and stability support

Topics #3 and 8 to be presented by Elisabeth C. Solano, Ph.D., Director, Pharmaceutical Development, Quark Pharmaceuticals

Course 4

Peptide-Oligonucleotide Conjugation Strategies

2:00 pm – 6:00 pm

Course Leader:
Michael Houston, Ph.D., Vice President, Chemistry and Formulations, Marina Biotech, Inc.

Session 1 The course will outline approaches to conjugate, purify and analyze peptide-oligonucleotide conjugations. Session 1 will address the various methods of conjugating peptide to oligonucleotides

  • Linker chemistry (amide, ester disulfide)
  • Solid phase versus solution phase conjugation
  • Monufunctional versus bifunctional linkers
  • Location and placement of linkers

Session 2 will address purification strategies for peptide-oligonucleotide conjugates

  • Purification methods applicable to conjugates (anion exchange and RP HPLC)
  • Desalting
  • Potential pitfalls and how to avoid them

Session 3 will address analytical methods and equipment

  • Analytical anion exchange HPLC
  • Ion pair RP-HPLC
  • LCMS and impurity profiles
  • Size exclusion chromatography

Dr. Houston leads both the oligonucleotide and peptide chemistry efforts at Marina Biotech including research and development activities. Previously, he held the position of Director of Chemistry at Cytovax Biotechnologies where he led the research and manufacturing efforts of the company's peptide-protein conjugate-based vaccine. Dr. Houston received his B.Sc. and Ph.D. in Chemistry from the University of Waterloo and completed a Postdoctoral Fellowship in Protein Engineering in the laboratory of Dr. Robert Hodges at the University of Alberta.

Course 5

Oligonucleotide Lead Discovery and Optimization to Candidate Selection

2:00 pm – 6:00 pm

Course Leader:
Satya Kuchimanchi, Ph.D., Associate Director, RNAi Lead Development, Alnylam Pharmaceuticals, Inc.

This course will discuss creative strategies for accelerating the process of oligonucleotide lead discovery, lead optimization and candidate selection, with an emphasis on successful translation from discovery to pre-clinical studies. Hear practical experiences and lessons learned on the path from discovery to IND from speakers representing leading oligonucleotide therapeutic companies.

You will learn about:

  • Novel chemistry motifs and platforms to accelerate candidate selection
  • Identifying chemistries for enhancing target specificity and in vivo stability
  • Sequence design and modifications to reduce immune responses and off-target effects
  • Strategies for identifying oligonucleotide candidates that will translate from in vitro to in vivo to pre-clinical studies
  • Library synthesis and creative molecular design strategies

Complimentary Special Event: Pre-Conference Forum · Sunday, May 20, 2012

CMO-Sponsor Relationships in Therapeutic Development - Expectations and Realities

4:00 pm – 6:00 pm

CMOs and Sponsors rely on each other for implementation of their respective business plans, but the working relationship can often be tense and difficult. The firms inhabit two very different worlds that only intersect at the point where they do business with each other. This course aims to generate better understanding of our different business models and the needs driving us, as a step towards improving the working relationships for all of us. It will consist of an opening plenary presentation by the course leader followed by separation into peptide- and oligonucleotide-specific groups for Audience Interactive Panel Discussions.
Mick McLean, Ph.D., CEO, Pro-Cure Therapeutics Ltd, United Kingdom

Follow Up Audience Interactive Panel Discussions

OLIGONUCLEOTIDES
Moderator:
Mick McLean, Ph.D., CEO, Pro-Cure Therapeutics Ltd, United Kingdom
Expert Panelists:
Kathryn L. Ackley, Ph.D., Vice President, Business Development and Project Management, Girindus America, Inc.
Paula Lorence, Vice President, Business Development & Project Management, Avecia
Paul Metz, Senior Director, Manufacturing Operations, Agilent Technologies, Inc.
James A. Powell, President, Meridian Consulting Services, Inc.
Stefan Vonhoff, Ph.D., VP CMC, Noxxon Pharma AG, Germany
Sanofi representative to be announced

PEPTIDES
Moderator:
Firoz D. Antia, Ph.D., Executive Director, Product Development, Palatin Technologies, Inc
Peptide Expert Panelists:
Mimoun Ayoub, Ph.D., Vice President, Global Business, Sales and Strategic Developments, Peptisyntha S.A., Member of the Solvay Group, Belgium
Matthieu Giraud, Ph.D., Director, Lonza Chemicals R&D Peptides, Lonza Ltd, Switzerland
Jon H. Rasmussen, Ph.D., Director of Technical Operations, PolyPeptide Laboratories AB, Sweden
Stacie Schroeder, Senior Vice President, Sales and Marketing, Bachem Americas, Inc.
Aleksander Swietlow, Ph.D., Principal Scientist, Amgen Inc.
David Tumelty, Ph.D., Associate Director, Chemistry, BioTherapeutics R&D, Pfizer Inc.

6:00
Welcome Networking Reception Co-Sponsored by and