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Gastrointestinal Drug Development: New and Existing Therapies
3 December - 4 December 2001
Gastrointestinal Drug Development: New and Existing Therapies
Although the GI drugs market is growing rapidly, at present, there is a distinct lack of targeted drug discovery for many gastrointestinal disorders, with few novel drugs reaching the marketplace.

SAE Media Group’s latest Pharmaceuticals conference, ‘Gastrointestinal Drug Development: New & Existing Therapies’ focuses on the challenges faced in gastrointestinal drug development and evaluation. The conference will examine current as well as emerging GI therapies and the strategic development of GI therapeutics to create successful drug portfolios. This conference will make sure that you are kept fully up to date with all the scientific and business news from the field of gastrointestinal drug development.

As you can see from the programme, SAE Media Group have strived to, and succeeded in getting expert speakers to discuss these key issues at the conference. These speakers will provide you with valuable insights into how to get the most out of the GI market through their presentations and discussions.

As with all SAE Media Group’s Pharmaceutical events, there will also be plenty of networking opportunities available allowing you to discuss the main issues with colleagues from all over the world.

Conference agenda

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8:30

Registration and Coffee

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9:00

Chairman's Opening Remarks

Dr Jörg Täubel

Dr Jörg Täubel, Consultant in Clinical Pharmacology, Charterhouse Clinical Research

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9:10

HUMAN TISSUES IN GI RESEARCH

Dr Richard Borman

Dr Richard Borman, Principal Scientist, Pharmagene

  • Use of human tissues in GI research
  • New indications for existing therapeutics
  • Using gene expression studies for target identification
  • Target validation – from gene to function
  • Novel treatments for Irritable Bowel Syndrome
  • Relevance of animal models in GI research
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    9:40

    DRUG DELIVERY

    Dr Verne Cowles

    Dr Verne Cowles, Director, Gastrointestinal Physiology, DepoMed

  • The Gastric Retention (GR) System
  • Improved absorption and bioavailability
  • Advantages of controlled release
  • Reducing gastrointestinal irritation
  • Evaluating the benefits
  • The future of drug delivery
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    10:20

    CREATING A GI PRODUCT PORTFOLIO

    Roly Bufton

    Roly Bufton, Chief Executive, Tillotts Pharma

  • Originator of Asacol, the world leading brand in IBD therapy
  • Colpermin: natural treatment for IBS
  • Purepa: a new, naturally based treatment for Crohn's disease
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    11:00

    Morning Coffee

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    11:20

    DEVELOPMENT & COMMERCIALISATION OF GI APPLICATIONS

    Dr Peter Meijlink

    Dr Peter Meijlink, General Manager, ForTe

  • The need for strategic product development
  • Improving efficacy
  • Time to market and cost control
  • Effective planning and implementation
  • Managing projects and partnering programmes
  • Future directions
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    12:00

    LEGAL ISSUES IN R & D COLLABORATION AGREEMENTS

    Matthew Warren

    Matthew Warren, Partner, Bristows

  • Legal structures for R & D collaborations
  • Ownership of intellectual property rights
  • Exploitation of intellectual property rights
  • Liability issues
  • Termination
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    12:40

    Networking Lunch

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    14:00

    THERAPY FOR IBD

    Dr Joseph Tami

    Dr Joseph Tami, Operations Manager, Clinical Development, Isis Pharmaceuticals

  • ISIS 2302
  • Achieving durable remission
  • Evaluating the long-term benefits of ISIS 2302
  • The future of Crohn’s treatments
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    14:40

    INFLAMMATORY BOWEL DISEASE

    Dr Tess Ambrose

    Dr Tess Ambrose, Development Project Manager, KS Buomedix

  • Challenges involved in developing drugs for UC
  • KSB304 – a novel treatment for ulcerative colitis
  • Colonic epithelial protein (CEP) and the inflammatory response in UC
  • Developing dosage at early stages
  • Targeting delivery to the colon
  • Solid dosage form: enabling self administration
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    15:20

    Afternoon Tea

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    15:40

    NOVEL GI TREATMENTS

    Dr Denis Headon

    Dr Denis Headon, President & Chief Scientific Officer, Agennix

  • Anti-microbial activity
  • Anti-inflammatory activity
  • Clinical studies in the prevention of infection
  • Applications in very low birth weight infants
  • Production of cGMP lactoferrin
  • Future applications
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    16:20

    TREATMENT OF GERD

    Dr Sheldon Sloan

    Dr Sheldon Sloan, Director, GI Medical Development, Department of Medical Affairs, Janssen Pharmaceutica

  • Disease overview
  • Improving control of gastric acidity
  • Therapeutic advances
  • Management of GERD
  • Maintenance of healing
  • Improving patient quality of life
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    17:00

    Chairman’s Closing Remarks and Close of Day One

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    8:30

    Re-registration and Coffee

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    9:00

    Chairman's Opening Remarks

    Dr Hans Graffner

    Dr Hans Graffner, Medical Director, & Vice President, Gastrointestinal Therapy Area, AstraZeneca

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    9:10

    IMPROVEMENT OF PPI THERAPY

    Dr Tore Lind

    Dr Tore Lind, Medical Director, & Global Product Team Physician, Nexium, AstraZeneca

  • Losec vs Nexium
  • The novel anti-ulcer agent - Nexium
  • Advantages of a single isomer
  • Improved therapy and alternative treatment for acid reflux
  • Gaining regulatory approval
  • Achieving long-term success in the anti-ulcer therapies market
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    9:40

    NOVEL TREATMENTS FOR HELICOBACTER PYLORI INFECTION

    Patrick McLean

    Patrick McLean, Vice Presidet and General Manager - Canada and Europe, Axcan Pharma

  • Current therapeutic treatments for H. pylori infection
  • Triple therapy - advantages
  • Pros and cons of current treatment regimes
  • The clinical need for a H. pylori vaccine
  • The potential of vaccine candidates
  • Future therapies for H. pylori
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    10:20

    DEVELOPING AN EFFECTIVE VACCINE

    Dr Giuseppe Del Giudice

    Dr Giuseppe Del Giudice, Senior Director, Chiron

  • Current issues in vaccine development
  • Strategic planning
  • Improving Helicobacter pylori infection rates
  • A promising approach to eradicating H. pylori
  • A promising approach to prevent H. pylori infection and complications
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    11:00

    Morning Coffee

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    11:20

    GASTRIC CANCER THERAPIES

    Dr Doriano Fabbro

    Dr Doriano Fabbro, Unit Head, in vitro Lead Profiliing, Novartis Oncology

  • Potential treatment of gastrointestinal stromal tumours
  • Phase I clinical trials as an anti-cancer therapy
  • Acting to reduce tumour size
  • Effective treatments with fewer side-effects
  • Future gastrointestinal anti-cancer therapeutics
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    12:00

    NO-ENHANCED ANTI-ULCERANTS

    Dr Gordon Letts

    Dr Gordon Letts, Chief Scientific Officer & Senior Vice President, Research & Development, NitroMed

  • The potential therapeutic advantage
  • NitRx technology
  • Enhancing the efficacy of existing medicines
  • Advantages of NO-technology
  • The future of gastric ulcer therapies
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    12:40

    Networking Lunch

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    14:00

    SHORT BOWEL TREATMENTS

    Dr Edward Nemeth

    Dr Edward Nemeth, Chief Scientific Officer, NPS Pharmaceuticals

  • ALX-0600 for gastrointestinal disorders
  • Current development strategies
  • Pilot phase II trial in short bowel syndrome
  • Ways to maximise absorptive area in the intestine
  • Drugs vs surgery
  • Maximising efficacy and minimising side-effects
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    14:40

    GASTROINTESTINAL MOTILITY DISORDERS

    Dr Andrew Sutton

    Dr Andrew Sutton, Partner & Medical Director, Guildford Clinical Pharmacology

  • Gastric motility methods
  • New applications of a non-invasive method
  • Applications of gut transit studies
  • Improving safety profiles of existing drugs as pointers to new drug opportunities
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    15:20

    Afternoon Tea

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    15:40

    A NEW LOOK AT MOTILIN AGONISTS

    Dr Robert Johnson

    Dr Robert Johnson, Vice President, Medical Affairs & Corporate Development, Kosan Biosciences

  • Current treatments
  • Improving on the early motilides
  • Developing “optimal” motilides at Kosan
  • Reducing tachyphylaxis
  • Fulfilling an unmet medical need
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    16:20

    SPEAKER PANEL

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    17:00

    Chairman's Closing Remarks and Close of Conference

    VENUE

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    51/53 Hatton Garden, London, United Kingdom

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    WHAT IS CPD?

    CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

    ‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

    CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

    Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

    CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

    CPD AND PROFESSIONAL INSTITUTES

    There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

    For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

    CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

    TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

    Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

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    As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

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