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RNA Therapeutics
10 February - 11 February 2025
RNA Therapeutics

SAE Media Group’s is proud to announce the 15th Annual RNA Therapeutics Conference, taking place on the 10-11 February 2025 in London, UK.


The RNA therapeutics industry has grown exponentially in recent years, largely attributed to the advancements in CRISPR RNA-editing technologies, and increased exposure of RNA vaccines following the COVID-19 pandemic. This upward trajectory is expected to continue, with 131 candidate therapies in clinical trials as of January 2024.


Don’t get left behind! Join us to discuss the latest advancements in RNA therapeutics with leaders from across the life science sector.
 

 Expect presentations and discussions addressing novel delivery methods and extra-hepatic delivery solutions, applications of AI for RNA sequence optimization and case studies of novel modalities progressing through the pipeline including circRNA, siRNA, miRNA, lncRNA and more. Further challenges that will be addressed include the lack of effective assays for in vivo analytical testing, including toxicity and immune-modulation considerations. We will also examine the rapidly changing regulatory landscape, identifying how the industry can adapt to meet changing guidelines and regulations.


Don't miss this opportunity to network with the pharma and biotech community of global experts in the UK and Europe; and help shape RNA therapeutic advancements! Our two-day agenda offers you peer-to-peer networking with Directors of key big pharma and biotech’s in the field, CEOs, Senior Scientists, Chief Medical Officers, Senior Vice Presidents and many more.
 

FEATURED SPEAKERS

Christalyn Rhodes

Christalyn Rhodes

Associate Vice President - Genetic Medicine - External Partnerships and Academic Collaborations , Eli Lilly

Christalyn Rhodes

Associate Vice President - Genetic Medicine - External Partnerships and Academic Collaborations , Eli Lilly
Christalyn Rhodes

Christalyn Rhodes, PhD is currently the Associate Vice President Genetic Medicine, External Partnering and Collaborations for Eli Lilly and Company  here she identifies opportunities, manages deals, and innovates nuanced strategies and collaboration agreements to develop genetic medicine strategically aligned with Eli Lilly core therapeutic areas. Additionally, Christalyn serves as the Expert-In-Residence for Harvard Innovation Labs, on the board of University of Massachusetts Medical School’s Bridge Fund, as well as an advisor to the Nucleate organization where she has supported the launch and advancement of several startups ranging from idea stage and brainstorming to securing funding. Previously, Christalyn worked as a Venture Capital Associate for Flagship Pioneering where she co-founded a biotechnological platform company to create novel therapeutics in the space of personalized genomic medicine. Dr. Rhodes received a Ph.D. in Biological Sciences from Harvard University and a BA from the University of North Texas.

Daniel Tondera

Head of Biology, Pantherna Therapeutics GmbH
Daniel Tondera

Daniel Tondera is an experienced expert in the field of RNA based therapeutics.
Before joining Pantherna Therapeutics, he was Group Leader at Silence Therapeutics where he was investigating the potential of using miRNAs and mRNA-based gene editing technologies for systemic LNP-mediated therapies. Prior to this he held positions as Group Leader at Cenix Bioscience in Dresden/Germany and as Senior Scientist at CRT in London/UK.
Daniel studied biochemistry at the University of Potsdam/Germany and received his PhD from the University of Potsdam in collaboration with Silence Therapeutics followed by postdoctoral training at the University of Geneva/Switzerland and at the Dana-Farber-Cancer Institute in Boston/MA.
 

Ekkehard Leberer

Scientific Advisor, NEUWAY Pharma
Ekkehard Leberer

Ekkehard serves as CEO at ELBIOCON (www.elbiocon.com) with more than 30 years of experience in biotechnology and pharmaceutical industry. He headed research teams and held managerial positions at the Biotechnology Research Institute of the National Research Council (NRC) of Canada in Montreal and in Big Pharma at Hoechst Marion Roussel, Aventis and Sanofi in Martinsried/Munich and Hoechst/Frankfurt. He was educated in chemistry and molecular biology at the University of Konstanz (Ph.D. and Habilitation in biochemistry) and University of Toronto (PostDoc at the Banting and Best Department of Medical Research). He is co-author of more than 60 publications in prestigious peer-reviewed journals including Nature and Science.
His scientific and managerial activities included responsibilities in functional genomics, genetic engineering, biological sciences, pre-clinical and clinical development of various therapeutic modalities encompassing small molecule drugs and biopharmaceuticals (peptides, antibodies, oligonucleotides, and mRNAs), drug delivery, portfolio management, external innovation, alliance management and business strategies.
Ekkehard served as a member in Scientific Advisory Boards of several biotechnology companies, and he was the Head of the Supervisory Board of BioM, Munich (www.bio-m.org). He is a member in the life sciences consulting network NewGuide (www.newguide.net).
 

Heinrich Haas

Chief Technology Officer, NeoVac
Heinrich Haas

Ph.D. in the group of Prof. Dr. Helmuth Möhwald at Johannes-Gutenberg Universität Mainz. Researched lipid membranes and organized bio-molecular systems. In pharmaceutical industry (Munich Biotech, Medigene, BioNTech) developed different types of nanoparticle products to clinical stage. Focus on advanced approaches for nanoparticle development and control.

Jay Sarkar

Researcher and Entrepreneur, Stanford University
Jay Sarkar

Dr. Sarkar has been in mRNA space for a little over a decade now. His work at Stanford University pioneered the use transiently expressed mRNAs to create an abridged epigenetic reprogramming regimen. This “transient or partial reprogramming” was shown to reset the age of a cell without erasing its identity. From this work, he spun out Turn Bio - the first company around this technology - and this approach has become a lead contender in longevity biotech space. He went on to found his current, new startup - reThink64 - that develops new paradigms for improving delivery of mRNAs and other large molecules.

Juha Monkare

Senior Scientist, Drug Product Development, Johnson & Johnson Innovative Medicine
Juha Monkare

Juha Monkare

Faculty of Health Sciences / School of Pharmacy, University of Eastern Finland
Juha Monkare

Ka-Wai Wan

Pharmaceutical Assessor, MHRA
Ka-Wai  Wan

Dr Ka-Wai Wan is a pharmacist by training and graduated from The School of Pharmacy (University of London). She completed her PhD in protein and gene delivery using nanomedicine at the Welsh School of Pharmacy (Cardiff, UK) and worked as a research academic for over a decade prior to her transition to the MHRA as a pharmaceutical assessor. She now leads on the assessment of nano-based medicinal products, providing scientific and regulatory advice on medicines, particularly on nanomaterials used for both small and macromolecules delivery. This includes nucleic acids delivery using lipid nanoparticles for a wide variety of medical applications.

Loic Roux

Co-Founder, Deep Science Ventures
Loic Roux

Lucas Bethge

Senior Scientist bei, Silence Therapeutics AG
Lucas Bethge

Lucas Bethge studied chemistry at the Humboldt-University zu Berlin (Germany). After he obtained his Ph.D. in 2011 in Bioorganic Chemistry, he first joined NOXXON Pharma. In 2016 he moved to Silence Therapeutics GmbH, a biotech company in Berlin that develops GalNAc-conjugated siRNA for therapeutic use. Currently, he is Vice-President and leading the Oligonucleotide Chemistry group at Silence Therapeutics. Lucas is an expert for the synthesis, conjugation, and analysis of oligonucleotides with over ten years of experience in industrial research and development at the interface between early research and clinical development.

Soren Ottosen

VP of Research, Sixfold Bioscience
Soren Ottosen

Steve Pascolo

Principal Investigator, University Hospital of Zurich and University of Zurich
Steve Pascolo

Trained as an immunologist at the Pasteur Institute (Paris, France), Dr. Steve Pascolo used mouse models to test and develop mRNA-based vaccines (direct injection of mRNA) during his post-doc in Tuebingen, Germany from 1998 till 2000. In 2000, he co-founded CureVac with Dr. Hoerr and Dr. von der Mulbe. Dr. Pascolo was Chief Scientific Officer (CSO) of the company from 2000 till 2006, developing the technology, implementing the worldwide first pharmaceutical (GMP) production of synthetic mRNA and starting in 2003 the worldwide first clinical studies where humans (including himself) got injections of in vitro transcribed mRNA. In 2006, he joined the oncology department of the University Hospital of Zurich, Switzerland and continued the development of immunotherapies based on RNA. In 2008, he founded Miescher Pharma to support this work. In 2013, he joined the dermatology department of the University Hospital of Zurich, Switzerland. In 2017, Dr. Pascolo implemented in the University of Zurich an academic mRNA platform https://www.cancer.uzh.ch/en/Research/mRNA-Platform.html. In collaboration with several research and clinical departments in Zurich he optimizes, tests and implements mRNA based vaccines and therapies.

Steven Hood

Director, Oligonucleotide ADME Strategy, DMPK, GSK
Steven Hood

Steven Hood

Director, Oligonucleotide ADME Strategy, DMPK, GSK
Steven Hood

Steve Hood received a PhD in Molecular Toxicology from the University of Surrey in 1993 and joined Glaxo Group Research as an Industrial Post doc in the Molecular Biology department in Greenford where he cloned and expressed CYPs in recombinant cell lines. Steve transferred to GlaxoWellcome at Ware in 1995 and became a manager in the new GSK DMPK Molecular Mechanism and Extrapolation Technology team in 2001. In 2010 Steve seconded to Scinovo and co-ordinated the GSK Oligo delivery (GOLD) project and was also Industrial co-lead of the IMI COMPACT consortium that ran from 2012-17 and evaluated delivery mechanisms for oligos and peptides. After a brief return to DMPK in 2015, Steve joined Bioimaging as a senior Scientific Director, responsible for the external imaging collaborations that are members of the Bioimaging Expertise Network (BEN). As part of this network, Steve was also Co-Director of the GSK Centre for Molecular Imaging (COMI) at the University of Illinois at Urbana Champaign, where he worked closely with Professor Stephen Boppart and his team.

In addition to his “day job”, Steve has spent most of the last 2 decades working on GSK’s diverse oligo portfolio and has supported projects ranging from inhaled SiRNAs, TLR antagonists, DMD exon skippers (Drisapersen) and ASOs for TTR (Innotersen) and HBV with Ionis (Bepirovirsen). More recently Steve has been involved with the Wave collaboration (Wve-006), the Jade HBV siRNA in licence project and the formation of the Boston Oligo hub.

In Jan 2024 Steve rejoined DMPK in and assume the role of Director of Oligo ADME Strategy. Steve will continue to develop the DMPK road map and train and mentor the next generation of DMPK Oligo Project Team Members and SMEs.
 

Urs Langen

Lab Head, Roche
Urs Langen

Urs Langen studied biochemistry at the University of Tübingen, Germany, before pursuing his PhD in vascular biology in the group of Prof. Ralf Adams at the Max Planck Institute in Münster, Germany. For his postdoctoral studies Urs joined the group of Prof. Chenghua Gu at Harvard Medical School in Boston, USA, where he investigated heterogeneity of the blood brain barrier in various brain areas. After completion of the postdoctoral project Urs joined Roche in Basel, Switzerland, where he has worked for 3 years as a senior scientist on drug delivery to the brain using the Roche Brainshuttle™ technology. Since 2024 Urs heads the Neurovascular Distribution Lab at Roche expanding his work on brain delivery of various drug modalities and leads multiple research projects in the dementia space. During his career Urs published numerous papers in high-impact peer-reviewed scientific journals including Nature and Nature Cell Biology.

Why you should attend:

  • Engage in the latest challenges in drug delivery and review the new and emerging alternatives to LNPs, that are broadening opportunities within tissue targeting.
  • Network with peers and industry experts to share ideas, discover novel solutions to some of the industry’s biggest challenges including biodistribution, controlling immunogenicity and increasing longevity of RNA therapeutic action.
  • Learn about novel modalities emerging in the space and the manufacturing and analytical strategies advancing development and synthesis of these RNA modalities.
  • Build your ecosystem within RNA therapeutics to uncover potential collaborators and keep pace with this rapidly-advancing field.

 Who should attend:

Any company striving to deliver optimal RNA therapies to patients in need.
If you or your company are working on or looking to break into any of the following areas, this conference is a must!

  • RNA therapeutic research and development
  • mRNA vaccines R&D
  • RNA therapeutic delivery methods
  • Analytical method development for oligonucleotide candidate testing
  • RNA manufacturing
  • RNA synthesis
  • Applications of AI within RNA vaccines and therapeutic development
     

Associate Vice President - Genetic Medicine - External Partnerships and Academic Collaborations
Eli Lilly
Head of Biology
Pantherna Therapeutics GmbH
Scientific Advisor
NEUWAY Pharma
Chief Technology Officer
NeoVac
Researcher and Entrepreneur
Stanford University
Senior Scientist, Drug Product Development
Johnson & Johnson Innovative Medicine
Faculty of Health Sciences / School of Pharmacy
University of Eastern Finland
Pharmaceutical Assessor
MHRA
Co-Founder
Deep Science Ventures
Senior Scientist bei
Silence Therapeutics AG
VP of Research
Sixfold Bioscience
Principal Investigator
University Hospital of Zurich and University of Zurich
Director, Oligonucleotide ADME Strategy, DMPK
GSK
Director, Oligonucleotide ADME Strategy, DMPK
GSK
Lab Head
Roche

VENUE

Hilton London Kensington

179-199 Holland Park Avenue, London, United Kingdom

At the heart of the Holland Park district, our hotel is 10 minutes from Westfield London shopping center. We're blocks from Shepherd's Bush Underground station, linking to central London, and Kensington Palace and Gardens are two miles from us. Enjoy 24-hour access to our fitness center.

 
Join us in WestEleven for hearty buffet breakfast, a great way to start the day! Our Avenue Bar and Lounge serves light bites throughout the day as well as a delicious, seasonal dining menu.”

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.
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Hilton London Kensington

179-199 Holland Park Avenue
London W11 4UL
United Kingdom

Hilton London Kensington

At the heart of the Holland Park district, our hotel is 10 minutes from Westfield London shopping center. We're blocks from Shepherd's Bush Underground station, linking to central London, and Kensington Palace and Gardens are two miles from us. Enjoy 24-hour access to our fitness center.

 
Join us in WestEleven for hearty buffet breakfast, a great way to start the day! Our Avenue Bar and Lounge serves light bites throughout the day as well as a delicious, seasonal dining menu.”
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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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