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Antibodies and Antibody Drug Conjugates
9 April - 10 April 2018
Antibodies and Antibody Drug Conjugates

SAE Media Group is proud to present their 6th annual Antibodies and Antibody Drug Conjugates conference on the 9th-10th of April 2018. The Antibody-drug Conjugates market is expected to reach USD 30 Billion by 2023*. http://bit.ly/2hxLtOS

Antibodies and antibody drug conjugates (ADCs) have the potential to make a groundbreaking impact upon medicinal therapies, diagnostics and characterization of diseases. There is massive potential for ADCs to be used in the development of targeted solid tumour therapies, due to their ability to act as precisely and effectively on target antigens. 

Key topics that will be covered in the upcoming event include: fragment drug conjugates, ADC payloads, site-selective ADCs/ site-specific conjugation and the best linker and warhead combinations.

Hear from some of the best minds in the industry and partake in valuable discussion with key leaders within the field at this topical and timely event!

Conference agenda

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8:30

Registration & Coffee

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9:00

Opening Remarks and Introductions

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9:10

Regulatory Strategy

Peter Bach

Peter Bach, Director, BioPharmaLogic Ltd.

  • Biology for the regulatory arguments
  • CMC for nonclinical development
  • Staging the test item supply to speed the development
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    10:00

    Taking the conjugate into the clinic

    Peter Bach

    Peter Bach, Director, BioPharmaLogic Ltd.

  • Geographical differences
  • Finding clinical leverage
  • Global option for FTIH
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    10:40

    Morning Coffee

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    11:10

    Non-Clinical

    Peter Bach

    Peter Bach, Director, BioPharmaLogic Ltd.

  • Models
  • Service providers
  • Data interpretation
  • In vitro and in vivo safety assessments:

    - Literature Based Risk Assessment
    - Immunohistochemistry
    - CRO selection, Study design and CROs management

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    11:50

    Final considerations

    Peter Bach

    Peter Bach, Director, BioPharmaLogic Ltd.

  • Bioanalytical considerations
  • Agency interactions
  • The regulatory package
  • Outsourcing strategy – test item supply: matching nonclinical needs to speed the development
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    12:30

    Closing Remarks and End of Workshop

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    13:30

    Registration & Coffee

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    14:00

    Chairman's Opening Remarks

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    14:10

    Antibody Structure and Function

  • Comparison of the five classes of antibodies and their determined binding specificity
  • Analysis of structure-function relationships for antibodies
  • Examination of C domains and how these mediate function
  • Antibody Bioinformatics and relationship to structure and function. INN naming system.
  • Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

    Kerry Chester

    Kerry Chester, Professor, University College London

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    14:50

    Antibody Biophysics

  • Biophysical characterization of antibodies and ADCs
  • Methods for the determination of antibody-antigen binding affinities
  • Where is the limit for analysis of antibodies using biophysical methods?
  • Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

    Kerry Chester

    Kerry Chester, Professor, University College London

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    15:30

    Afternoon Tea

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    16:00

    Antibody Discovery

  • Analysis of sources (origins) of different antibodies
  • Strategies to accelerate antibody discovery
  • A look at current and emerging Antibody Discovery Technologies
  • Accelerating antibody discovery by protein expression
  • Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

    Kerry Chester

    Kerry Chester, Professor, University College London

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    16:40

    Antibody Conjugation

  • Methods of Antibody conjugation
  • Why is antibody-drug conjugation useful
  • The chemistry behind Antibody-Drug Conjugates
  • Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

    Kerry Chester

    Kerry Chester, Professor, University College London

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    17:20

    Closing Remarks

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Philip Howard, Chief Scientific Officer, Spirogen

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    9:10

    Use of modelling and simulation to compare new generation HER-2 ADCs with Kadcyla™: a focus on PK and efficacy

    Alison Betts

    Alison Betts, ADC Scientist, Pfizer

  • Kadcyla is a HER-2 ADC approved in 2013 for patients with HER2+ metastatic breast cancer
  • Kadcyla is only efficacious in high HER2 tumors and patients are acquiring resistance
  • New generation HER-2 ADCs are being designed to overcome these limitations
  • PK/PD  methodologies for efficacy and safety differentiation will be presented
  • For PK predictions a mechanistic target mediated drug disposition model is proposed accounting for binding to shed HER-2 extracellular domain and variability across patients
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    9:50

    Application of a PK-PD Modeling & Simulation in Antibody-Drug Conjugate Development

    Aman Singh

    Aman Singh, PK-PD Scientist, Janssen

  • Preclinical to clinical translation
  • Bystander effect of ADCs
  • Binding site barrier of ADCs
  • Cell-level pharmacokinetics of ADCs
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    10:30

    Morning Coffee

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    11:00

    GlycoConnect™ and HydraSpace™ technologies for superior Antibody-Drug Conjugates

    Sander van Berkel

    Sander van Berkel, Director R&D Operations, Synaffix

  • Head-to-head comparison demonstrates superiority of Glycan-Conjugated ADCs (GlycoConnect™) versus mainstream technologies 
  • Readily adaptable HydraSpace™ enables highly hydrophobic payloads, dual warhead ADCs and further expands TI
  • Decomposition of Parameters Contributing to the Improved Therapeutic Index
  • GlycoConnect™ and HydraSpace™
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    11:40

    Antibody Targeted Amanitin Conjugates (ATACs) - Expanding the ADC landscape with a new payload targeting RNA Polymerase II

    Andreas Pahl

    Andreas Pahl, CSO, Heidelberg Pharma

  • Antigen-Targeted Amanitin-Conjugates (ATACs) represent a new class of ADCs using the payload Amanitin.
  • This payload introduces a novel mode of action into oncology therapy, the inhibition of RNA polymerase II.
  • The technology platform includes Amanitin supply, site-specific conjugation, demonstrated safety profile and biomarker.
  • HDP-101 is the first ATAC directed against BCMA entering Phase I trials by the end of 2018
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    12:20

    Networking Lunch

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    13:30

    Minor-Groove binding DNA-interactive molecules as ADC Payloads - the impact of sequence-selectivity and mono-alkylation versus cross-linking

    David E. Thurston

    David E. Thurston, Professor of Drug Discovery, King's College London

  • The impact of mono-alkylation versus intra- and interstrand cross-linking mechanisms of action on the in vitro and in vivo efficacy and toxicity of ADC payloads and ADCs.
  • Is there an opportunity to match the sequence-selectivity of DNA-interactive payloads to the genetic profiles of tumour types?
  • Is there an opportunity to improve the therapeutic window of ADCs by “tuning” the mechanism of action and sequence-selectivity of the payload?
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    14:10

    PBDs – update on an efficient and effective payload class

    Arnaud Tiberghien

    Arnaud Tiberghien, Scientist II, Chemistry, Spirogen

  • A potent and flexible class of ADC payloads and their industrial processing viability.
  • Whether or not PBDs make better payloads than others.
  • Comparison of PBD DNA crosslinkers and PBD DNA alkylators
  • New PBD payloads in developments. Consequences on mode of action, efficacy and tolerability
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    14:50

    Afternoon Tea

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    15:20

    Novasep’s integrated solutions for ADCs

    Francois D'Hooge

    Francois D'Hooge, Head of Bioconjugation, Novasep S A S

  • Simplifying the supply chain through an integrated offer
  • Design considerations of a dedicated conjugation facility
  • Novasep’s strengths for ADCs: case studies
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    16:00

    Precision cancer therapy ADCs with novel target, antibody and cancer toxin technologies

    Robert Boyd

    Robert Boyd, UK Site Head and Scientific Director, Oxford BioTherapeutics

  • Selection of novel ADC cancer targets in the post-genomics era
  • Improved efficacy by optimizing targets to ADC technologies
  • Target Selection criteria - how to choose the best target for your specific need
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    16:40

    Chairman’s Closing Remarks and Close of Day One

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

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    9:10

    Antibody-Pyrrolobenzodiazepine Conjugates

    Philip Howard, Chief Scientific Officer, Spirogen

  • An overview of the PBB ADC Clinical landscape
  • Present 3 case studies on PBD-ADCs for haematological indications
  • Present 1 case study on a PBD-ADC in a solid indication
  • Case studies will include both clinical and preclinical data
  •  

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    9:50

    Site-selective ADCs by disulfide bridging

    James Baker

    James Baker, Chemistry Lecturer, University College London

  • Site-selective ADCs offer the prospect of improved Therapeutic Indexes over traditional heterogeneous conjugation approaches, and are likely to form the basis of next generation ADCs.
  • Can achieve such site-selectivity by targeting the four interchain disulfide bonds (in IgG1s), using bridging reagents which reconnect the two cysteine residues.
  • We describe the development of Next Generation Maleimide reagents, and the related Pyridazinediones, as optimised platforms for ADCs constructed in this way.
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    10:30

    Morning Coffee

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    11:00

    Antibody Fragment Drug Conjugates (FDCs): A tailored therapy for solid tumours

    Mahendra  Deonarain

    Mahendra Deonarain, Chief Scientific and Operating Officer, Antikor Biopharma Ltd.

  • Discovery of antibody fragments specifically designed for FDCs
  • Manufacture of FDCs and payload screening
  • In vivo pharmacokinetics and tumour cure efficacy in gastric cancer models
  • Rodent models for toxicology and tolerability
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    11:40

    Design principles for maximizing the drug delivery efficiency and therapeutic index of ADCs

    Robert Lyon

    Robert Lyon, Senior Director Protein Sciences, Seattle Genetics Ltd

  • The conjugation of drug-linkers to an antibody can result in increased nonspecific uptake and catabolism in healthy tissues
  • This phenomenon has two potential negative consequences—unintended delivery of the drug to non-target tissues, and diminished exposure of the tumor to the ADC
  • Careful design of the drug-linker can minimize this effect in preclinical models, with demonstrable decreases in drug concentrations in normal tissues paired with maximal delivery to the tumor
  • Toxicology and xenograft studies indicate that the optimized design both decreases off-target toxicity and improves antitumor activity, and we are currently planning to evaluate this design clinically with an anti-CD48 antibody for patients with multiple myeloma
     
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    12:20

    Networking Lunch

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    13:30

    Highly Potent APIs (HPAPIs) in ADC projects

    Justin Mason-Home

    Justin Mason-Home, Director, HPAPI Project Services Limited

  • ADC Toxicants in the context of Pharma HPAPIs
  • Other ADC Component Hazards
  • Health and Safety Project Elements in Designing and Delivering HPAPI Projects
  • Risk Assessment, Risk Communication and Risk Management
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    14:10

    Anthracycline-based antibody drug conjugates with potent immune-stimulatory functions

    Roger Beerli

    Roger Beerli, CSO, NBE Therapeutics

  • Site-specific conjugation using sortase enzyme (SMAC™-Technology), yielding homogenous ADCs.
  • Highly potent payload, providing access to difficult-to-address targets.
  • Anthracycline-based payload with attractive IO properties.
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    14:50

    Afternoon Tea

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    15:20

    The use of Nanobody formatting to improve immune-oncology therapeutics

    Carlo Boutton

    Carlo Boutton, Director of Technology, Ablynx

  • Small Nanobodies® with their modular design are a perfect starting point for generating multivalent and multispecific therapeutics for immune modulation.
  • The power of the platform and its flexibility to develop optimal drug formats will be demonstrated by a multivalent approach for an agonistic Nanobody against the co-stimulatory immune checkpoint receptor GITR and a multispecific T-cell recruitment format.
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    16:00

    The use of bispecific antibodies to modulate anti-tumour immune responses

    Delphine Buffet

    Delphine Buffet, Senior Research Associate, F-star

  • Bispecific antibodies: an attractive alternative to cancer treatments combinations
  • F-star’s approach to create bispecific mAb²
  • In vitro and in vivo efficacy of F-star bispecific antibodies targeting oncology pathways
  • clock

    16:40

    Chairman’s Closing Remarks and Close of Day Two

    Official Media Partner

    Supporters

    VENUE

    Copthorne Tara Hotel

    Scarsdale Place, Kensington, London, United Kingdom

    The Copthorne Tara Hotel London Kensington is an elegant contemporary four-star hotel in prestigious Kensington, located just a two minutes walk from High Street Kensington underground station, making exploring easy. The hotel offers well-appointed and comfortable guest rooms combining Standard, Superior and Club accommodation. Club rooms offer iconic views over the city and include Club Lounge access for complimentary breakfast and refreshments. Guests can sample the authentic Singaporean, Malaysian and Chinese cuisine at Bugis Street, traditional pub fare at the Brasserie Restaurant & Bar or relax with a delicious drink at West8 Cocktail Lounge & Bar.

    The Copthorne Tara Hotel boasts 745 square meters of flexible meeting space, consisting of the Shannon Suite and the Liffey Suite, ideal for hosting conferences, weddings and social events. Facilities include access to the business centre 24 hours a day, fully equipped fitness room, gift shop, theatre desk and Bureau de Change. With ample onsite parking outside the London congestion charge zone and excellent transport links via Heathrow Airport, the hotel is the perfect location for business or leisure stays. The hotel is within close proximity to the shops of High Street Kensington, Knightsbridge and Westfield London, Olympia Conference Centre, Royal Albert Hall, Kensington Palace and Hyde Park.

     

    A number of our clients have been approached by third party organisations offering to book hotel rooms. We would advise that you do not book through them as they are not representing the SMi Group. SMi Group books all hotel rooms directly. If you are approached by a third party organisation then please contact us before making any bookings. If you have already booked a hotel room using a third party organisation, we would highly recommend contacting the hotel you were booked into to ensure a booking has been made for you. We would also advise you to please check the terms and conditions of the booking carefully.
    HOTEL BOOKING FORM

    [SPEAKER INTERVIEW] - Robert Lyon, Senior Director Protein Sciences, Seattle Genetics

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    [ATTENDEE LIST] - LIST OF COMPANIES & JOB TITLES

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    [SPEAKER INTERVIEW] - Mahendra Deonarain, Chief Executive and Scientific Officer, Antikor Biopharma

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    [2016 PRESENTATION] - SKAN

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    [2016 PRESENTATION] - NBE Therapeutics

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    [SPEAKER INTERVIEW] - Alison Betts, Associate Research Fellow, Pfizer

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    Media Partners


    ADC Review

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    ADC Review / Journal of Antibody-drug Conjugates (ISSN: 2327-0152) is an international publication combining professional social media with an online-only, hybrid open-access, peer reviewed journal. The Journal aims to serve the needs of a diverse community of individuals including academia, life sciences, pharma, (basic, translational and clinical) research, clinicians, along with regulatory affairs, government authorities and representatives from payers, and policy makers. Key information includes peer-reviewed articles, news features, discussions, blogs, and a knowledge center offering the latest and most relevant information about Antibody Drug Conjugates (ADCs), BiSpecific Antibodies, Site Specific Antibody Drug Conjugates, Small Molecule Drug Conjugates (SMDC), and Engineered Antibody Fragments. The purpose of the Journal is to present this information in an understandable and a useful format for all stakeholders.

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    Copthorne Tara Hotel

    Scarsdale Place
    Kensington
    London W8 5SR
    United Kingdom

    Copthorne Tara Hotel

    The Copthorne Tara Hotel London Kensington is an elegant contemporary four-star hotel in prestigious Kensington, located just a two minutes walk from High Street Kensington underground station, making exploring easy. The hotel offers well-appointed and comfortable guest rooms combining Standard, Superior and Club accommodation. Club rooms offer iconic views over the city and include Club Lounge access for complimentary breakfast and refreshments. Guests can sample the authentic Singaporean, Malaysian and Chinese cuisine at Bugis Street, traditional pub fare at the Brasserie Restaurant & Bar or relax with a delicious drink at West8 Cocktail Lounge & Bar.

    The Copthorne Tara Hotel boasts 745 square meters of flexible meeting space, consisting of the Shannon Suite and the Liffey Suite, ideal for hosting conferences, weddings and social events. Facilities include access to the business centre 24 hours a day, fully equipped fitness room, gift shop, theatre desk and Bureau de Change. With ample onsite parking outside the London congestion charge zone and excellent transport links via Heathrow Airport, the hotel is the perfect location for business or leisure stays. The hotel is within close proximity to the shops of High Street Kensington, Knightsbridge and Westfield London, Olympia Conference Centre, Royal Albert Hall, Kensington Palace and Hyde Park.

     

    HOTEL BOOKING FORM

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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.

    ‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

    ‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

    The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

    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.

    GLOBAL CPD

    Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

    CPD Certificates

    We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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    Contact SAE Media Group

    UK Office
    Opening Hours: 9.00 - 17.30 (local time)
    SAE Media Group , Ground Floor, India House, 45 Curlew Street, London, SE1 2ND, United Kingdom
    Tel: +44 (0) 20 7827 6000 Fax: +44 (0) 20 7827 6001
    Website: http://www.smgconferences.com Email: events@saemediagroup.com
    Registered in England - SMi Group Ltd trading as SAE Media Group




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