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RNA Therapeutics

Selective inhibition of gene expression by RNA interference (RNAi) and wider oligonucleotide methods hold the potential to address significant unmet medical needs with importance across major disease areas such as cancer, genetic disorders, cardiovascular disease and autoimmune disorders.  Recent advances in small interfering RNA delivery and target selection provide unprecedented opportunities for clinical translation and positioning in the market place.

This conference offers the opportunity to engage with strategies for advancing RNAi–based therapies for rare and major diseases through devlopment and clinical trials to market, case study updates on approaches to optimising RNAi formulation and delivery and hear lessons learned through successful submissions from regulators.
 

FEATURED SPEAKERS

Annemieke Aartsma-Rus

Annemieke Aartsma-Rus

Associate Professor , Leiden University Medical Center
Bo Rode Hansen

Bo Rode Hansen

VP, Drug Discovery & Alliance, Roche
David Blakey

David Blakey

Chief Scientist, AstraZeneca
Nagy Habib

Nagy Habib

Chairman and Co-Founder, MiNA Therapeutics
Rodger Novak

Rodger Novak

CEO, CRISPR Therapeutics

Annemieke Aartsma-Rus

Associate Professor , Leiden University Medical Center
Annemieke Aartsma-Rus

Axel Vater

VP Drug Discovery and Preclinical Research, Noxxon Pharma AG
Axel Vater

Bård Smedsrod

Chief Scientific Officer, D'Liver
Bård Smedsrod

Bo Rode Hansen

VP, Drug Discovery & Alliance, Roche
Bo Rode Hansen

Claude Paul Malvy

Professor, Universite Paris Sud
Claude Paul Malvy

Covadonga Paneda

R&D Manager, Sylentis
Covadonga Paneda

David Blakey

Chief Scientist, AstraZeneca
David Blakey

Dirk Haussecker

Consultant, RNA Therapeutics
Dirk Haussecker

James Legg

Patent Attorney , Boult Wade Tennant
James Legg

Jesper Wengel

Professor, BioNEC Center Director, University of Southern Denmark
Jesper Wengel

Joerg Kaufmann

Chief Scientific Officer, Silence Therapeutics
Joerg Kaufmann

John Johnston

Clinical Assessor, Biologicals & Biotechnology Unit, MHRA
John Johnston

Michael Khan

Chief Medical Officer, Silence Therapeutics
Michael Khan

Michael Kormann

Group Leader, Pediatric Infectiology and Immunology, Eberhard-Karls-University Tuebingen
Michael Kormann

Nagy Habib

Chairman and Co-Founder, MiNA Therapeutics
Nagy Habib

Rodger Novak

CEO, CRISPR Therapeutics
Rodger Novak

Ryszard Kole

Distinguished Scientist, Sarepta Therapeutics
Ryszard Kole

Steffen Panzner

Managing Director, Lipocalyx
Steffen Panzner

Stephen Hart

Professor in Molecular Genetics , UCL
Stephen Hart

Steven Hood

Director, Scinovo, GSK
Steven Hood

Sven Klußmann

Co-Founder & Chief Technology Officer, Noxxon Pharma
Sven Klußmann

Victor Kotelianski

Director of the Centre for Research, Education and Innovation, Skolkovo Institute of Science and Technology
Victor Kotelianski

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

Claude Paul Malvy

Claude Paul Malvy, Professor, Universite Paris Sud

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9:10

RNAi therapeutics: Opportunities, obstacles and solutions

Michael Khan

Michael Khan, Chief Medical Officer, Silence Therapeutics

• Challenges for developing effective RNAi - based drugs
• Research on better delivery systems
• Validation in NHPs
• Identifying the right targets and indications
• Update on clinical status of Atu027
 

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9:40

RNAi therapeutics for eye conditions

Covadonga Paneda

Covadonga Paneda, R&D Manager, Sylentis

• Update on the clinical programme of Bamosiran, an siRNA for the treatment of glaucoma
• New designs and candidates: impact on biodistribution within the eye
• Advantages of RNAi therapeutics in ophthalmology
 

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10:10

Morning Coffee

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10:40

From Bench to Bedside – The evolution of mirror-image oligonucleotides as new therapeutic modalities

Axel Vater

Axel Vater, VP Drug Discovery and Preclinical Research, Noxxon Pharma AG

• The benefits of Spiegelmers
• Preclinical & clinical data
• Overview NOX-E36 (drug for diabetic nephropathy)
 

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11:10

RNA activation in therapy

Nagy Habib

Nagy Habib, Chairman and Co-Founder, MiNA Therapeutics

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11:40

CRISPR-Cas as a “can opener” for genome editing?! First insights into early translational work for human therapeutics

Rodger Novak

Rodger Novak, CEO, CRISPR Therapeutics

• Introduction to CRISPR-Cas – a scientific thriller
• What makes CRISPR-Cas special? – Differentiation regarding other gene editing technologies
• Perspective provided on potential for translation into human medicines – challenges and opportunities
• CRISPR-Cas as a role model for personalized medicine
 

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12:10

Hepatic targeting and avoidance of oligonucleotide drugs: What is the real story?

Bård Smedsrod

Bård Smedsrod, Chief Scientific Officer, D'Liver

• Understanding hepatic uptake of large molecule drugs, including oligonucleotides
• Compare uptake activity in different types of liver cells
• Insights into uptake receptors and metabolism
• A need for new ways of explaining hepatotoxicity caused by uptake of large molecule drugs
 

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12:40

Networking Lunch

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13:40

The use of LNA/UNA-aptamers for anticancer and delivery purposes

Jesper Wengel

Jesper Wengel, Professor, BioNEC Center Director, University of Southern Denmark

• Locked nucleic acid (LNA) is a structurally rigid modification that increases the binding affinity of a modified-oligonucleotide
• Compare the synthetic routes to both of these modifications, contrast the structural features, examine the hybridization properties of LNA and UNA modified duplexes
• LNA and UNA are also emerging as versatile modifications for aptamers

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14:10

Transfection: Viral and synthetic techniques converge

Steffen Panzner

Steffen Panzner, Managing Director, Lipocalyx

  • What can be learned from viral delivery?
  • Convergence between a viral and synthetic system
  • Development of the Viromer technology
  • Cell uptake and delivery data
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    14:40

    Delivering macromolecules to the right address - many hands make light work

    Steven Hood

    Steven Hood, Director, Scinovo, GSK

    • Synthesis of drug/polyterpene bioconjugates
    • Design of the nanoassemblies and their functionalization with recognition ligands
    • Cell and tissue imaging
    • Pharmacological evaluation in vitro (cell culture) and in vivo
     

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    15:10

    Afternoon Tea

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    15:40

    Protecting biotech inventions, how much for how little?

    James Legg

    James Legg, Patent Attorney , Boult Wade Tennant

    • Why use a patent to protect a biotech invention?
    • An underlying principle - The extent of patent protection should be justified by the technical contribution to the art.
    • Application of this principle during prosecution of patent applications and post-grant
    • Implications for when to file and what to include in your patent application
     

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    16:10

    Quick Tips

    John Johnston

    John Johnston, Clinical Assessor, Biologicals & Biotechnology Unit, MHRA

    • The hypothesis and the objective of a clinical study
    • Clinical end points / surrogate markers
    • The Innovation Office at the MHRA
    • Points will be illustrated by examples in the public domain
     

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    16:40

    Biochemically modified messenger RNA encoding nucleases for in vivo gene correction of severe inherited lung diseases

    Michael Kormann

    Michael Kormann, Group Leader, Pediatric Infectiology and Immunology, Eberhard-Karls-University Tuebingen

    • Modified messenger RNA
    • In vivo treatment
    • Life-saving efficacy
    • Limiting off-target effects

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    17:10

    Round Table Discussion –Developing RNA therapeutics for rare diseases

    Michael Kormann

    Michael Kormann, Group Leader, Pediatric Infectiology and Immunology, Eberhard-Karls-University Tuebingen

    • Identifying and facing early stage and clinical challenges
    • How to best understand and seizing opportunities in the market place

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    17:50

    Chairman’s Closing Remarks and Close of Day One

    Claude Paul Malvy

    Claude Paul Malvy, Professor, Universite Paris Sud

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Michael Khan

    Michael Khan, Chief Medical Officer, Silence Therapeutics

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    9:10

    RNA Therapeutics: The 3rd major engine of pharmaceutical value creation?

    Dirk Haussecker

    Dirk Haussecker, Consultant, RNA Therapeutics

    • Review of RNA Therapeutics technology
    • Current state of RNA Therapeutics clinical pipeline
    • Assessment of RNA Therapeutics pre-clinical pipeline
    • RNA Therapeutics business and financial market considerations
     

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    9:40

    RNA Therapeutics: Unlocking the potential with locked nucleic acids

    Bo Rode Hansen

    Bo Rode Hansen, VP, Drug Discovery & Alliance, Roche

    • What is new after several decades of learnings from developing RNA therapeutics?
    • Why has the success rate of RNA therapeutics drug development been low with very few marketed drugs as result?
    • What is the most recent thinking on how to increase the productivity of RNA therapeutics development?
    • Why has Roche recognized Locked Nucleic Acids as the preferred chemistry and modality for RNA therapeutics development?
     

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    10:10

    Networking towards clinical application of antisense mediated exon skipping

    Annemieke Aartsma-Rus

    Annemieke Aartsma-Rus, Associate Professor , Leiden University Medical Center

    • Overview of how exon skipping can be exploited to treat different diseases with unmet medical need
    • Discussion of path from proof of concept to clinical trials using Duchenne muscular dystrophy as a showcase
    • Discussion of joint efforts to overcome translational challenges for clinical implementation

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    10:40

    Morning Coffee

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    11:10

    Tackling Intractable targets in oncology – progress towards viable therapeutic oligonucleotides platforms

    David Blakey

    David Blakey, Chief Scientist, AstraZeneca

    • Robust activity in tumours has been limited with initial  ASO chemistries
    • Next generation ASOs demonstrate  robust target knock down in multiple preclinical cancer models including primary tumour explants  and human tumour xenografts
    • AZD9150, a constrained ethyl ASO vs STAT3 has completed initial trials in cancer patients and shown encouraging signs of clinical activity
    • Preclinical and clinical data will be shared that suggest next generation ASO technology is poised to become a key therapeutic modality to modulate intractable oncology targets

     

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    11:40

    Panel Debate - Collaborative working from academia to big pharma

    Michael Khan

    Michael Khan, Chief Medical Officer, Silence Therapeutics

  • Preparing to colaborate with big pharma - do's and dont's
  • Exploring collaborative models
  • The role of platform providers

     

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    12:20

    Networking Lunch

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    13:30

    In vivo RNAi and functional genomics

    Victor Kotelianski

    Victor Kotelianski, Director of the Centre for Research, Education and Innovation, Skolkovo Institute of Science and Technology

    • The use of siRNAs in vivo to study gene function in the liver of mouse models
    • Demonstration of progress in siRNA delivery to mouse hepatocyte
    • RNA interference to examine the activities of specific genes in animal models
    • Analysis of three different cases of multiple mRNAs knockdown in studies of endocytosis, hypoxia and HYPPO pathway
     

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    14:00

    From RNA splicing to Eteplirsen trials: a drug for Duchenne muscular dystrophy (DMD)

    Ryszard Kole

    Ryszard Kole, Distinguished Scientist, Sarepta Therapeutics

    • Invention of RNA splicing modulation
    • From thalassemia to DMD
    • Insight in to Eteplirsen induced exon skipping of 51 in dystrophin pre-mRNA in DMD patients
    • The results of the continuing trial after 120 weeks of treatment will be presented

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    14:30

    Afternoon Tea

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    15:00

    Fusion-oncogene junctions in cancer and interfering RNA: A review

    Claude Paul Malvy

    Claude Paul Malvy, Professor, Universite Paris Sud

    • Double targeting for Ewing sarcoma
    • A  new siRNA delivery agent for Ewing cells
    • Literature review of siRNA and other cancers with fusion oncogene

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    15:30

    Taking siRNA beyond the liver: Multifunctional nano-complexes for targeted siRNA delivery to brain, lung and tumours

    Stephen Hart

    Stephen Hart, Professor in Molecular Genetics , UCL

    • Targeted lipid-peptide nanocomplex formulations: modulation of surface properties for improved targeting specificity and toxicity profiles
    • Self-assembly protocols by microfluidics for improved siRNA nanoparticle homogeneity, stability and storage
    • Silencing of therapeutic targets in tumour, lung and brain
    • Therapeutic efficacy of siRNA nano-complexes by systemic delivery to tumours
     

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    16:00

    Chairman’s Closing Remarks and Close of Day Two

    Michael Khan

    Michael Khan, Chief Medical Officer, Silence Therapeutics


    Associate Professor
    Leiden University Medical Center
    VP Drug Discovery and Preclinical Research
    Noxxon Pharma AG
    Chief Scientific Officer
    D'Liver
    VP, Drug Discovery & Alliance
    Roche
    Professor
    Universite Paris Sud
    R&D Manager
    Sylentis
    Chief Scientist
    AstraZeneca
    Consultant
    RNA Therapeutics
    Patent Attorney
    Boult Wade Tennant
    Professor, BioNEC Center Director
    University of Southern Denmark
    Chief Scientific Officer
    Silence Therapeutics
    Clinical Assessor, Biologicals & Biotechnology Unit
    MHRA
    Chief Medical Officer
    Silence Therapeutics
    Group Leader, Pediatric Infectiology and Immunology
    Eberhard-Karls-University Tuebingen
    Chairman and Co-Founder
    MiNA Therapeutics
    CEO
    CRISPR Therapeutics
    Distinguished Scientist
    Sarepta Therapeutics
    Managing Director
    Lipocalyx
    Professor in Molecular Genetics
    UCL
    Director, Scinovo
    GSK
    Co-Founder & Chief Technology Officer
    Noxxon Pharma
    Director of the Centre for Research, Education and Innovation
    Skolkovo Institute of Science and Technology

    Sponsors and Exhibitors

    Official Media Partner

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    Interview Dirk Haussecker

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    Interview with Michael Kormann

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    Sponsors and Exhibitors


    Lipocalyx

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    http://www.lipocalyx.de/

    Lipocalyx is active in nucleic acid delivery. Our Viromers are novel synthetic vectors emulating viral uptake and endosome escape and provide a safe and efficient way to deliver siRNA, mRNA or DNA. The company was founded in 2011 in Halle(Saale), a German biotech hub. Lipocalyx is offering off-the shelf research reagents and development services for the industry.


    Silence Therapeutics Plc

    Sponsors and Exhibitors
    www.silence-therapeutics.com

    Silence Therapeutics is a leading RNA therapeutics company. It has developed proprietary modifications to improve the robustness of RNA sequences together with advanced liposomal chemistries to enhance the delivery of its therapeutics. Its technology can selectively silence or replace the expression of any gene in the genome, modulating expression up as well as down in a variety of organs and cell types, in vivo. This allows the development of therapeutics for diseases with high unmet clinical need.

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    http://www.pharmavoice.com

    PharmaVOICE magazine, and its supporting VIEW publications, provide commentary about the challenges and trends impacting the life-sciences industry, covering a range of issues from molecule through market. PharmaVOICE's more than 41,000 U.S.-based subscribers are also kept abreast of the latest trends through additional media resources, including WebSeminars, Podcasts, Videocasts, and White Papers.


    PMR

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    http://www.pmrcorporate.com

    PMR (www.pmrcorporate.com) is a British-American company providing market information, advice and services to international businesses interested in Central and Eastern European countries as well as other emerging markets. PMR's key areas of operation include business publications (through PMR Publications), consultancy (through PMR Consulting) and market research (through PMR Research ). Being present on the market since 1995, offering high international standards in projects and publications, as well as providing one of the most frequently visited and top-ranked websites, PMR is one of the largest companies of its type in the region.


    Swiss Biotech Association

    Supporters
    http://www.swissbiotech.org/

    The Swiss Biotech Association (SBA) is the national industry association for biotechnology, including pharmaceuticals, diagnostics, agriculture, food, cosmetics, environmental biotechnology, and specialty chemicals. Members are companies active in modern biotechnology, such as R&D, Production, Marketing and Sales, Finance, Services and Consulting. SBA provides a networking platform for Life Science clusters, academic and federal institutions the like. Founded in March 1998, the Association grows steadily.

    Marriott Regents Park

    128 King Henry's Road
    London NW3 3ST
    United Kingdom

    Marriott Regents Park

    This 4 star north London hotel in zone 2 is the perfect destination for the astute business traveler as well as the leisure guest that knows how convenient north London hotels are, as a base from which to explore the city .Bond Street is just 3 stops from Swiss Cottage underground station on the Jubilee Line, so you can be shopping, exploring the sights and taking in one of London’s world-renowned West End shows in less than 15 minutes when you stay at this hotel near central London. At the same time, the hive of activity that is Camden Town, the chic shops, cafes and restaurants of Primrose Hill and ZSL’s London Zoo in Regents Park are all just a short walk from this hotel in north London.

    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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