QSAR - Neurodegenerative Disorders 2004

From: Lorraine Lescure <lorraine.lescure>
Date: Thu, 19 Feb 2004 15:12:24 -0000

> Neurodegenerative Disorders 2004
> 31st March & 1st April 2004 Marriott Kensington Hotel, London
>
> Neurodegenerative therapies will be one of the
> defining growth areas over the next 10-20 years:
> * With an aging population, cases of alzheimer's, parkinson's and
> similar diseases will increase exponentially
> * Also, as new treatments are developed, more cases will become
> treatable,and for longer..
> * Both these factors will lead to an an economic windfall for
> pharmaceutical/biotech companies that embrace this sector.
>
> Full analysis of current market AND future developments:
> * Case studies of current drug treatments (eg. Mirapex, Rilutek)
> * Pipeline/Early market drugs - Antegren, Axura.
> * The impact/viability of gene therapy/stem cell treatments.
> * Other novel treatments - eg. surgical implantation
> * Plus much more analysis...FULL AGENDA BELOW.
>
> Network with key speakers at Neuro 2004, who will include:
>
> Dr. Stephen Donoghue, VP of Clinical Development, Europe, Elan
> Dr. Beth Hoffman, Head Neuroscience Discovery Research, Eli Lilly
> Dr. Hans Basun, Senior Clinical Research Physician, AstraZeneca
> Dr. Donna Barten, Senior Research Investigator, Neuroscience Drug Discovery, Bristol-Myers Squibb
> Dr. Michel Dib, Medical Director for Internal Medicines Department, Aventis
> Dr Chriso Babatsikos, International Product Manager Pramipexole, Boehringer-Ingelheim
> Dr. Gerald Yakatan, President and CEO, Avanir Pharmaceuticals
> Prof. Alan Kingsman, Chief Executive Officer, Oxford BioMedica
> Eric Kmiec, Chief Scientific Officer, NaPro Bio Therapeutics
> Dr. Christian Gilles, Director, R&D & Head, CNS Ageing Research, Forenap
> Friedhelm Klingenburg, Senior VP for Corporate Development, Merz Pharmaceuticals
> Dr. Eti Yoles, Vice President Product Research and Development, Proneuron Biotechnologies
> Helen Hodges, Head of Functional Assessment Group, ReNeuron
> Adele Rowley, Director, Pharmacology, Cellzome
>
>
> Who should attend Neurodegenerative Disorders 2004 ?
>
> *> Heads of Clinical Research, CNS
> *> Heads of Clinical Development/ VP Clinical Development
> *> Heads of R&D (Pain/CNS/Depression)
> *> Heads of CNS therapeutics
> *> Global Brand Area, CNS
> *> Heads of Pre-Clinical Development, CNS
> *> CNS Clinical Project Management
> *> Heads of Neuroscience Research
> *> Business Development Executives
> *> Directors of Strategic Planning and Development
> *> Chief Medical Officers
> *> Chief Scientific Officers
> *> Research Scientists
>
> Also included in this 2 day conference is an interactive pre-conference workshop,
> a more intimate working environment, ideal for networking opportunities:
>
> Surrogate Markers in Central Nervous System Drug Development
> Workshop Leader: Professor Tonmoy Sharma, Clinical Neuroscience Research Centre
> Tuesday 30th March 2004
>
> - PRICING -
> Attend the:
> 2 Day conference with interactive workshop - ONLY GBP1400 plus VAT(17.5%)
> 2 Day conference - ONLY GBP1099 plus VAT(17.5%)
> Workshop only - ONLY GBP650 plus VAT(17.5%)
>
> - BOOKINGS -
> Booking is easy, simply contact Lorraine Lescure on:
> Telephone: +44 (0)20 8767 6711
> Fax: +44 (0)20 8767 5001
> Email: lorraine.lescure{}visiongain.com
> Terms and conditions apply - see below.
>
> Please find below the conference agenda. To book your place at
> Neurodegenerative Disorders 2004 simply give me a quick ring or email
> stating whether you require a single place or a group booking.
>
> I look forward to hearing from you soon.
>
> Regards
>
> Lorraine Lescure
> Account Manager
> Visiongain b2b Conferences
> Tel: +44 (0) 20 8767 6711
> mailto:lorraine.lescure~!~visiongain.com
>
>
>
> Pre Conference workshop -
> Surrogate Markers in Central Nervous System Drug Development
>
> Tuesday 30th March 2004
> Workshop Leader: Professor Tonmoy Sharma
> Clinical Neuroscience Research Centre
>
> Examine the relationship between brain and behaviour using a>
> variety of surrogate makers:
>
> *> Use of Cognitive Function
> *> Startle Response
> *> Eye Movements
> *> Critical Flicker Fusion
> *> Evoked Potential
> *> Electronic Data Capture
>
>
> Full conference agenda
>
> Day One
>
> Wednesday 31st March 2004
>
>
> Conference Chairperson
> Dr. Donna Barten
> Senior Research Investigator, Neuroscience Drug Discovery
> Bristol-Myers Squibb
>
> 9:00 Registration and coffee
>
> 9:30 Opening remarks from the Chair
>
> INTRODUCTION TO NEURODEGENERATIVE DISORDERS
>
> 9:45 How to Identify Novel Molecular Targets for
>
> Neurodegenerative Disorders?
> *> Pathologic insight to disease targets
> *> Identifying genes, SNPs and proteomic analysis
> *> What are the pathways to novel targets?
> *> End game of target validation
>
> Dr. Beth Hoffman
> Head Neuroscience Discovery Research
> Eli Lilly
>
> 10:20 What are the Issues in the Development of Drugs for Neurodegenerative Disorders?
>
> *> Importance of safety assessment
> *> What is the proof of concept?
> *> Advantages and disadvantages of human models
> *> Biomarkers/ surrogate markers
> *> Can we avoid lengthy patient studies?
> *> What about the placebo affect?
>
> Dr. Christian Gilles
> Director, R&D & Head, CNS Ageing Research
> Forenap
>
> 11:00 Morning Coffee
>
> ALZHEIMER'S DISEASE
>
> 11:20 Causes of Alzheimer> '> s Disease and Treatment Options
>
> *> Aetiology of disease
> *> Current treatment options
> *> Amyloid hypothesis of AD
> -Secretase Inhibitors
> -Immunotherapy
> -Aggregation Inhibitors
> *> Secretase Inhibitors
> *> Targeting tau in AD
>
> Dr. Hans Basun
> Senior Clinical Research Physician
> AstraZeneca
>
> 12:00 Use of Secretase Inhibitors in Animal Models of AD
>
> *> What are the characteristics of secretase inhibitors?
> *> Comparison of transgenic mice with Alzheimer's disease
> *> Tg2576 and YAC-APP transgenic mice
> *> Guinea pig models
> *> Transgenic rat models
>
> Dr. Donna Barten
> Senior Research Investigator
> Neuroscience Drug Discovery
> Bristol-Myers Squibb
>
> 12:40 Lunch
>
> 14:00 CASE STUDY: Will Axura be the First Drug for Treating
> Moderate-to-Severe Alzheimers?
>
> The only drugs approved for Alzheimer's disease are indicated for
> mild-to-moderate patients. Number of major pharma companies are
> currently developing therapies for moderate-to-severe indications.
> Axura entered the European Market in 2003 and set to enter the
> US in 2004.
>
> *> What are the sales expectations and reasons why?
> *> First Alzheimer's drug to be indicated for moderate-to-severe
> patients
> *> Advantages: Merz estimates the drug could delay the need to
> transfer patients to long-term care and reduce level of care
> required by over 50 hours a month
>
> Friedhelm Klingenburg
> Senior VP for Corporate Development
> Merz Pharmaceuticals
>
> 14:40 Cellzome's Alzheimer's Disease Drug Discovery Programme
>
> *> What is the major focus of Alzheimer> '> s Disease drug discovery
> programmes?
> - inhibition of amyloid formation
>
> *> Cellzome> '> s approach: proteomics technology
> - Tandem Affinity Purification procedure
> - LC/MS-MS protein mass spectrometry capabilities
>
> *> Analysis: over 200 molecular associations in APP processing and
> novel interaction of regulatory and modulatory importance
> identified
>
> Adele Rowley
> Director, Pharmacology
> Cellzome
>
> 15:20 Afternoon Tea
>
> AMYOTROPHIC LATERAL SCLEROSIS
>
> 15:40 CASE STUDY: Rilutek, The only Drug Approved for Treating
> Amyotrophic Lateral Sclerosis
>
> *> ALS : a good model for the development in the degenerative
> disease
> - lesson from rilutek
>
> *> Only approved drug for treatment of ALS by the FDA
> *> How does it work?
> *> Development and potential in the new indications
>
> Dr. Michel Dib
> Medical Director for Internal Medicines Department
> Aventis
>
> 16:20 CASE STUDY: Phase III results of Neurodex for Treating
> Pseudobulbar Affect
>
> *> What is pseudobulbar affect?
> - seen in numerous neurodegenerative disease
>
> *> Neurodex technology overview>
>
> *> Clinical and regulatory development status
> - first half of phase III studies completed with ALS patients
> - second half of phase III studies in progress with MS patients
>
> Dr. Gerald Yakatan
> President and CEO
> Avanir Pharmaceuticals
>
> 17:00 Questions and Discussion
>
>
> Day Two Thursday 1st April 2004
>
> 09:00 Coffee
>
> 09:30 Opening Remarks from the Chair
>
> PARKINSON'S DISEASE
>
> 09:45 CASE STUDY: Leading Therapy for PD, Mirapex by Boehringer
> Ingelheim and Pharmacia
>
> Dopamine agonists entered the market in the 1980's- PD market was
> worth $1.2 billion in 2002 with 60% of its value coming from the
> sale of dopamine agonists.
>
> *> Parkinson's disease market profile: levodopa, dopamine agonists
> and COMT inhibitors
> *> Mirapex had 17% of market share in 2002- What are the reasons
> for its success?
> *> Research showing slower rate of decline in dopaminergic neuronal
> functioning in patients receiving Mirapex to those treated with
> levodopa
> *> Implications
>
> Dr. Chriso Babatsikos
> International Product Manager Pramipexole
> Boehringer-Ingelheim
>
> 10:20 CASE STUDY: Surgical Interventions- Activa Parkinson's
> Control Therapy by Medtronic
>
> *> Implantation Procedure
> *> How does it work?- counteraction of dyskinetic movements
> *> FDA approval for expanded use
> *> What is the future of the surgical interventions market for PD?
>
> Pino Carbone
> Business Manager - Activa Therapy
> Medtronic Europe
>
> 11:00 Morning Coffee
>
> 11:20 Is Gene Therapy a Viable Option for Treating PD?
>
> ProSavin is being developed by Oxford BioMedica, which utilises the
> company's proprietary lentivirus and involves the transfer of the
> tyrosine hydroxylase gene with a dopamine turnover inhibiting gene.
> *> What are the requirements for molecular genetic analysis?
> *> How to deliver genes to the nervous system?
> *> Targets and models
> *> Update on the clinical development of ProSavin
> *> What are neuro-protective approaches for Parkinson's disease?
>
> Prof. Alan Kingsman
> Chief Executive Officer
> Oxford BioMedica
>
> 12:00 Can Brain Stem Cell Transplantation be used for CNS Repair?
>
> *> What are the advantages?
> *> What risks are present?
> *> Transplant strategies
> *> Graft effects in animal models of neurodegnerative disease:
> functional and structural integration
> *> What are the mechanisms of graft activity?
> *> Prospects for clinical applications
>
> Dr. Helen Hodges
> Head of Functional Assessment Group
> ReNeuron
>
> 12:40 Lunch
>
> 14:00 Opening Remarks from the Chair
>
> MULTIPLE SCLEROSIS
>
> 14:10 CASE STUDY: Antegren, A Novel Approach to MS Treatment
> by Elan
>
> *> Results of Antegren clinical trials for relapsing MS
> *> Different mechanism of action from any other approved MS drug
> *> Advantages of Antegren?
>
> Dr. Stephen Donoghue
> VP of Clinical Development, Europe
> Elan
>
> 14:50 Therapeutic Plasma Exchange (TPE) for MS and other CNS
> Demyelinating Diseases
>
> *> TPE: evidence of efficacy in CNS demyelinating diseases
> *> What are the clinical factors predictive of response to TPE?
> *> What are the pathological factors involved in response to TPE?
> *> Theories of mechanisms of action
>
> Dr. Mark Keegan
> Consultant
> Department of Neurology
> Mayo Clinic and Foundation
>
> 15:30 Afternoon Tea
>
> HUNTINGTON'S DISEASE
>
> 15:50 How can the Immune System be Harnessed for Attenuating
> Neurodegeneration?
> *> Autoimmunity is a beneficial physiological response to CNS trauma
> *> What are the safe ways to induce a protective immune response?
> *> Incubated macrophages in spinal cord injury - Phase I clinical study
> *> Therapueatic vaccination for neurodegenerative disorders - PN277
>
> Dr. Eti Yole
> Vice President Product Research and Development
> Proneuron Biotechnologies>
>
> 16:30 The Feasibility of Using Synthetic DNA Oligonucleotides to
> Prevent Htt Aggregation in Huntington's Disease
>
> *> Is synthetic DNA an effective therapeutic agent for many disease
> indications?
> *> Functions as an anti-sense molecule, RNAi , a gene correction
> agent and perhaps an apatamer
> *> Toxicity studies and immunogenic responses
> *> What is the potential of using short modified oligonucleotides to
> disrupt the process of aggregate formation in Huntington's
> Disease?
>
> Eric Kmiec
> Chief Scientific Officer
> NaPro Bio Therapeutics
>
> 17:00 Questions and Discussion
>
> 17:20 Chairman Summation
>
> 17:30 Close of Conference
>
>
>
>
>
>
>
>
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>
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Received on 2004-02-19 - 12:40 GMT

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