Programme Book

Total Page:16

File Type:pdf, Size:1020Kb

Programme Book SPONSORS AND EXHIBITORS MAIN MAJOR Programme book CIS - INDUSTRY SPONSORED SYMPOSIA OCTOBER 5-8 www.ever.be EVER K SIS - SPECIAL INTEREST SYMPOSIA boo MME A R G 2016 in conjunction ro EUPO EXHIBITORS Science for Sight course with EVER CAMBRIDGE RESEARCH SYSTEMS NICE EVER 2016 P EVER 2016 THANK YOU EVER would like to thank all of its past and present sponsors We would especially like to thank the following companies, many of which are our long-term supporters, for their generous sponsorship in 2016 Thanks to their kind support EVER can continue to encourage research and dissemination of knowledge concerning the eye and vision by means of meetings, publications and exchange of information EVER 2016 - programme book 22 CME XEN_Advertisement_A4 portrait_Ever2016 programme.indd 1 Find alist of countries where XEN is available at the Allergan stand. Adverse events should be reported to your local regulatory authority and Allergan office. XENDate is ofnot preparation:commercially July available 2016 INT/0457/2016a XEN in France. is amedical device class III CE 0086. Please consult your local directions for use. The power of simplicity Rethink glaucoma management glaucoma Rethink 09/08/2016 10:59 HERMES RHODES 1 RHODES 2 RHODES 3 RHODES 4 GALLIENI 1&2 GALLIENI 4 GALLIENI 5 Friday, October 7, 2016 08:30 - 10:00 RV - Confrontation of G - New technologies in COS - Nanotechnology in PO - Conjunctival tumors EUPO 1 LC - Ocular damage from ACB - Stem cells and MBGE - Grand rounds in OCT-angiography and glaucoma surgery ophthalmology Neuro-ophthalmology ambient optical radiation cell therapy advances in ophthalmic genetics fluoresceine angiography ophthalmology POURNARAS C - VANDEWALLE E - COUPLAND S - ZOGRAFOS L STALMANS I KOMPELLA UB - GRIFFITH M CAUJOLLE JP SÖDERBERG P - WEGENER A PETROVSKI G - MOE M LEROY B - HAMEL C 10:10 - 10:40 Keynote Lecture: OPA1 gene and mitochondrial optic neuropathy: disease mechanisms and potential therapies - VOTRUBA M Hermes 10:40 - 11:00 Coffee break Exhibition area 11:00 - 12:30 ARVO@EVER - Animals in RV - FP session - COS - FP session - Corneal PO - Controversies in EUPO 2 PO/IM - Cytology of IM - FP session - Nov- MBGE/LC - Radiation ocular oncology AMD & miscellaneous transplantation from the posterior uveal Neuro-ophthalmology atypical inflammation or elties in diagnosis and induced cataracts tumors treatment in ocular lab to the OR melanoma immunology VAN GINDERDEUREN R - COUPLAND S SOUBRANE G - LEYS A GICQUEL J - FUCHSLUGER T MOURIAUX F - CASSOUX N VAN CALSTER J BODAGHI B - WILLERMAIN F AINSBURY L - WEGENER A 13:30 - 15:00 RV - Retinal detachment G - EVER Obergurgl optic COS/RV - Emerging PO - Topical and EUPO 3 EOVS - FP session - IM - How to publish your MBGE - FP session nerve meeting intravitreal pharma- solutions in Neuro-ophthalmology Electrophysiology - scientific work? symposium: the ageing ophthalmology cotherapy in ocular optic nerve oncology protocols & applications GRUS F - CROWSTON J - FUCHSLUGER T - ZOGRAFOS L - CASTELO-BRANCO M - BUJAKOWSKA K - POURNARAS JA - E MER Y MARTIN K STEFANSSON E DESJARDINS L KRASTEL H PLEYER U SCHWARZ N 15:00 - 16:00 Poster session2: Neuro-ophthalmology / Strabismology / Paediatric/History • Retina / Vitreous Poster area 16:00 - 16:30 Business meeting RV Business meeting EOVS / G Business meeting COS / NSPH Business meeting PO / PBP EUPO 4 Business meeting IM / MBGE Business meeting ACB Business meeting LC 16:30 - 18:00 FAN Club G - Implications of COS - Corneal OOG Session 1 Neuro-ophthalmology PBP - Ocular pulse IM - FP session - New in- GOA - Update on severe Case presentations neuro-glial interactions neovascularization and amplitude - from pole to sights in imaging in ocular allergic conjunctivitis in neurodegenerative immune privilege pole immunology diseases KOLKO M - KIVELÄ T - ABEGAO PINTO L - BREMOND-GIGNAC D - WAAGEPETERSEN H HORI J - CHEN L - ZHANG H HADJISTILIANOU T MARQUES-NEVES C HERBORT CP - NERI P FAUQUERT J 18:00 - 18:30 EVER General Assembly Hermes Saturday, October 8, 2016 08:30 - 10:00 NSPH/RV - The first ones COS - Keratoconus COS - Corneal infectious OOG Session 2 & EUPO 5 FRO: Belgian Fund for in ophthalmology diagnosis and treatment diseases Business Meeting Strabismus Research in in the clinical practice Ophthalmology - part 1 SZENTMARY N - GICQUEL J - TASSIGNON MJ - GRZYBOWSKI A - ASCASO F ZSOLT NAGY Z BREMOND-GIGNAC D HEEGAARD S - CASSOUX N CASPERS L 10:00 - 10:20 Coffee break Exhibition area EUPO 6 10:20 - 10:50 Ophthalmic Research Lecture: The cataract surgeon and the anterior interface - TASSIGNON M-J Strabismus Hermes 10:50 - 12:00 Poster session 3: Anatomy / Cell Biology • Cornea / Ocular Surface • Immunology / Microbiology Lens and Cataract • Pathology / Oncology Poster area 12:00 - 13:00 Lunchtime Women 4 EVER COS - Pseudophakic and COS - Maximising success OOG Session 3 FRO: Belgian Fund for 13:00 - 14:30 EUPO 7 phakic toric implants – in deep anterior lamellar Research in from preoperative keratoplasty Strabismus Ophthalmology - part 2 examination LANGENBUCHER A - ZOGRAFOS L - TASSIGNON MJ - Creuzot C SZENTMARY N - EPPIG T DUA H S - GICQUEL J DESJARDINS L CASPERS L 14:30 - 15:00 Prize Award Ceremony & Closing Remarks Hermes EVER 2016 Word from the President Dear EVER members, colleagues and friends, 2016 heralds an exciting and animated month of October as EVER and EUPO (the European Professors of Ophthalmology group) come together for a grand event. This meeting is not to be missed! As in previous years, EVER offers a varied menu of fundamental fare and house specialties. These in- clude board preparation sessions, clinical courses, topic-specific symposia, state-or-the-art research platforms, keynote lectures and a broad palette of scientific posters The “extra” in 2016 will be the EUPO courses dedicated to neuro-ophthalmology and strabismus. These are CME accredited courses which will run in parallel with the EVER scientific program during Friday and Saturday (October 7-8). EUPO courses are intended to assist the preparation of young ophthalmologists for the European Board of Ophthalmology examination and also serve as excellent refresher courses for any practicing ophthalmologist. I am delighted to announce that EVER offers open general admission to EUPO courses for all EVER meeting registrants (without an increase in registration fee from the previous year!). Likewise, EUPO attendees will have open access to the EVER program on those 2 shared days. And as EVER and EUPO boast a strong international faculty, this is a win-win situation for all! At EVER, we strive for growth, advancement and improvement in ophthalmology and visual science. This may sound like the oft-heard rally cry of “more, bigger and better” which, in practice, often trans- lates to harried, stressed and rushed. Rest assured that EVER is none of that. The beautiful relaxed atmosphere of the French Riviera is once again home to the EVER meeting. Over 4 sunny days in Nice, after the scientific day, enjoy a stroll through the fresh market , take a dip in the Mediterranean waters and savor tasty gourmet dishes on an open terrace. So join me at EVER-EUPO 2016. It will be a stimulating experience! Aki KAWASAKI President EVER 2016 EVER 2016 - programme book 1 L’innovation en Ophtalmologie va bien au-delà des médicaments Téléchargez l’Application Retina Base pour tablettes tactiles sur l’App Store® ou le Google Play® et découvrez plus de 120 cas cliniques de pathologies rétiniennes rédigés par des experts, disponibles en Français et en Anglais. • NNaviguez à travers l’organisation planétaire des pathologies et ccas cliniques. • RRecherchez facilement les clichés grâce au moteur de rrecherche intuitif et ltrez les résultats par mot-clé, technique dd’imagerie et auteur. • RRecevez les noti cations dès que de nouveaux cas sont ddisponibles. Rendez-vous sur www.viaopta.fr pour découvrir ou redécouvrir tous les services ViaOpta™ dédiés à l’ophtalmologie C65306 - Août 2014 Votre partenaire en Ophtalmologie C65306 ViaOpta_210x297.indd 1 06/04/2016 11:44 EVER 2016 Table of contents Word from the president ....................................................................................................................................1 About EVER ..........................................................................................................................................................4 Composition of the board 2016 .........................................................................................................................8 Congress information ....................................................................................................................................... 10 Grants and prizes ..............................................................................................................................................14 Floorplan ............................................................................................................................................................16 Partners of EVER ...............................................................................................................................................18 About the programme book ............................................................................................................................20 Scientific sections 2016 .....................................................................................................................................21 Industry Sponsored Symposia ........................................................................................................................22
Recommended publications
  • Robert Maclaren
    INTERVIEW IN CONVERSATION WITH Robert MacLaren, Professor of Ophthalmology, University of Oxford Professor Robert MacLaren gave the Keeler Lecture at the Royal College of Ophthalmologists Annual Meeting in May 2019 on gene therapy for retinitis pigmentosa. We caught up with him afterwards to find out more. people in the developed world, since we now well and we will have treatments available have treatments for diabetic retinopathy. for our patients in the UK, but we’re not quite There is a huge unmet need. We have also got there yet. one gene that has been approved so it is up to us to try and find other genes and get them What do you hope will be made through to clinical trials. possible through gene therapy in the future? There was a lot of media attention The ideal, of course, would be to prevent earlier this year about gene therapy someone from going blind who would trials in age-related macular otherwise loose their sight from a genetic degeneration (AMD). How would disease. Genetic mutations are occurring What are the key messages of your this work? all the time, so when you have a baby, for Keeler Lecture? The concept of gene therapy is to use a virus instance, that child will have 70 mutations Gene therapy is now actually an approved to deliver a gene under the retina to the that are not in the DNA of either the mother treatment, so it is not just about research, retinal epithelium. We’ve demonstrated or the father. Most of them are silent and do but it’s actually something patients can have.
    [Show full text]
  • Retinal Gene Therapy
    Robert MacLaren – [email protected] 26 Update RETINA contact ChoroideraemiaRETINAL trial shows GENE promise and THERAPY challenges of viral gene replacement approach by Howard Larkin in Milan clinical trial of gene therapy for choroideraemia While choroideraemia is relatively rare, afflicting about one now under way in the UK provides an opportunity in 50,000 in northern Europe with the highest incidence in for ophthalmologists to contribute to what Finland, it is a promising disease entity for gene therapy for could be a revolution in treating genetic retinal several reasons, Prof MacLaren noted. conditions,A Robert E MacLaren, DPhil, FRCS, FRCOphth, of For one, the choroideraemia phenotype is specific and Oxford University, Oxford Eye Hospital and Moorfields Eye instantly recognisable, whereas the appearance of the retina Hospital, London, UK, told the 12th EURETINA Congress. in other types of retinitis pigmentosis is similar regardless of Viral-vector gene therapy holds the promise of curing the gene involved. This makes possible early identification of life-long genetic retinal disorders with a single injection choroideraemia patients. Also, the gene involved, CHM, is 1.9 of replacement genetic material, Prof MacLaren said. The kilobases long, making it an ideal size for delivery by adeno- treatment he developed with Prof Miguel Seabra, Imperial associated viral vectors, which have been shown safe and Courtesy of Robert E MacLaren, DPhil, FRCS, FRCOphth College, London, is the first for choroideraemia, an x effective for retinal applications, Prof MacLaren said. Figure 1: European collaboration. Prof Robert MacLaren (UK) performs the first chromosome-linked degenerative retinal disease leading to In addition, the condition typically progresses slowly, from choroideraemia gene therapy surgery in Oxford with Dr Martin Zinkernagel (Switzerland).
    [Show full text]
  • Congress 2015 Final Programme
    The Royal College of Ophthalmologists Annual Congress of Ophthalmologists College The Royal Innovation Annual Congress 2015 19 - 21 May 2015 19 - 21 May Ophthalmology is changing. We believe the future of ophthalmology is single-use. Advances in understanding. That’s the reason we Final Programme Innovations in patient safety, develop over one hundred technology and technique. single-use products each year and Abstracts Malosa work alongside for pioneering procedures surgeons from throughout the such as ReLEx, DSAEK & ophthalmic profession. Femto-Phaco. 19-21 May 2015 - The ACC Liverpool Developing instruments to So, whatever advances lie ahead, we remain at the enable the procedures of the and Abstracts Final Programme future. cutting edge. +44 (0) 870 3000 555 www.malosa.com RCO Advert 2015.indd 1 19/03/2015 12:39 New AlaHeavy new possibilities see us at Stand J New AlaHeavy, from Alamedics Germany is a new ‘heavy oil’ which addresses some of the shortcomings of similar products that have been available in the past. AlaHeavy is a silicone oil which has been manufactured to be of a higher density than water. AlaHeavy is not a mixture. AlaHeavy is not oil with added density-enhancing surfactants, such as alkanes or alkenes. That means no separation during storage, or in the eye, as well as less chance of an inflammatory reaction within the eye. AlaHeavy also gives you 2 further ‘bonus’ advantages. It exhibits a higher density but lower viscosity than similar products currently on the market. Therefore, not only is it more effective as a heavy tamponade, but it is also easier to handle.
    [Show full text]
  • New Trial for Blindness Rewrites the Genetic Code 20 March 2017
    New trial for blindness rewrites the genetic code 20 March 2017 However, a research team led by Professor Robert MacLaren from the University of Oxford has reprogrammed the genetic code of RPGR to make it more stable, but in a way that does not affect its function. This has allowed the gene to be delivered reliably by a viral vector into retinal cells. The current trial is the first in the world to test a treatment for retinitis pigmentosa caused by RPGR. Robert MacLaren, Professor of Ophthalmology at the University of Oxford, who is leading the trial New trial for blindness rewrites the genetic code. Credit: said: "The effect of RPGR-related disease on Shutterstock families with retinitis pigmentosa is devastating and we have spent many years working out how to develop this gene therapy. Changing the genetic code is always undertaken with great caution, but Researchers have started a new gene therapy the new sequence we are using has proven to be clinical trial to treat X-linked retinitis pigmentosa highly effective in our laboratory studies. (XLRP), the most common cause of blindness in young people. "The genetic code for all life on Earth is made up of four letters – G, T, A and C. In RPGR, however, Retinitis pigmentosa is currently untreatable and half of the gene comprises only two letters – A and leads to a slow and irreversible loss of vision. G. This makes the gene very unstable and prone to mutations, making it a lead cause of blindness in The trial is being run by Nightstarx Ltd (Nightstar), patients with retinitis pigmentosa.
    [Show full text]
  • Oxford Univ Spin Off Gets $20 Mn for Retinal Gene Therapy
    Oxford Univ spin off gets $20 mn for retinal gene therapy 04 February 2014 | News | By BioSpectrum Bureau Singapore: Syncona, an independent subsidiary of the Wellcome Trust, has made a $19.60 million (£12 million) investment in NightstaRx, which is a spin-out from the University of Oxford and its research commercialization company Isis Innovation. Nightstar will focus on the development and commercialization of therapies for retinal dystrophies, which are degenerative conditions affecting vision. The company's first programme is a gene therapy for an inherited form of progressive blindness called choroideremia developed by Professor Robert MacLaren at Oxford's Nuffield Laboratory of Ophthalmology. The gene therapy uses a small modified virus, AAV.REP1 to deliver the correct version of the choroideremia (CHM) gene to cells in the retina of the eye. The vector used to treat choroideremia, AAV.REP1, was developed by a team of researchers, led by Professor Robert MacLaren of the University of Oxford, and is currently being studied in a 12 patient phase I clinical trial supported by the Wellcome Trust and Department of Health. Mr Chris Hollowood, partner, Syncona, and Nightstar's chairman, commented that, "We are delighted to be working with Professor MacLaren to provide the support required to bring this important therapy to choroideremia patients. We have appointed Dr Melanie Lee as CEO of Nightstar, an experienced industry professional with both scientific and business acumen and we will augment the team over the coming weeks." Mr Tom Hockaday, MD, Isis Innovation, said that, "The £12 million investment in Nightstar represents one of the largest investments in a new academic spin-out in Europe.
    [Show full text]
  • Annual Report 2015 Our Vision to Restore Hope and Sight
    ANNUAL REPORT 2015 OUR VISION TO RESTORE HOPE AND SIGHT OUR MISSION TO LEAD THE FIGHT AGAINST BLINDNESS BY ADVANCING RETINAL DISEASE RESEARCH, EDUCATION AND PUBLIC AWARENESS TABLE OF CONTENTS MESSAGE FROM THE PRESIDENT & CEO and BOARD CHAIR MESSAGE FROM THE PRESIDENT & CEO 1 and BOARD CHAIR 2 RESEARCH MOVING VISION Sharon Colle, Andrew Burke, 4 SCIENCE FORWARD President & CEO Board Chair Dear Friends, A CANADIAN FIRST 7 For the Foundation Fighting Blindness, 2015 was a break-through year. Committed supporters like you funded the very first gene-therapy clinical trial for an eye disease in 2015 Canada. Over four decades of dedication and research led to this critical FUNDRAISING EVENTS 8 turning point. VISION QUEST 2015 This clinical trial is just one of the many shining examples of incredible milestones that 9 demonstrate the accelerating pace of vision research. We will be able to go further, faster, thanks to you. 2015 10 LEADERSHIP DONORS In 2015 alone, your generosity supported a total of 28 ongoing research projects across Canada for a total investment of $1.64 million. Thank you! 2015 CORPORATE 11 EVENT SPONSORS Finding treatments and cures for blinding eye diseases is now possible, and the impact of & MONTHLY DONORS these discoveries for Canadians living with vision loss will be life changing. As we move forward, we must intensify our efforts, and lean in to the fight against blindness. 12 2015 FINANCIALS It’s up to us, together, to turn our tremendous hope into reality. Sincerely, BOARD OF DIRECTORS & 14 SCIENTIFIC ADVISORY BOARD Sharon Colle Andrew Burke President & CEO Board Chair 1 Research Sites Our Patient Registry Sites 2014 Vision Quest Events RESEARCH DR.
    [Show full text]
  • Genetic Manipulation for Inherited Neurodegenerative Diseases: Myth Or Reality? Patrick Yu-Wai-Man1,2,3
    BJO Online First, published on August 1, 2016 as 10.1136/bjophthalmol-2015-308329 Review Br J Ophthalmol: first published as 10.1136/bjophthalmol-2015-308329 on 21 March 2016. Downloaded from Genetic manipulation for inherited neurodegenerative diseases: myth or reality? Patrick Yu-Wai-Man1,2,3 1Wellcome Trust Centre for ABSTRACT genetic manipulation seems an obvious solution as Mitochondrial Research, Rare genetic diseases affect about 7% of the general a radical means of correcting the primary patho- Institute of Genetic Medicine, Newcastle University, population and over 7000 distinct clinical syndromes logical process that contributes to neuronal dys- Newcastle upon Tyne, UK have been described with the majority being due to function and disease progression. 2Newcastle Eye Centre, Royal single gene defects. This review will provide a critical Victoria Infirmary, Newcastle overview of genetic strategies that are being pioneered upon Tyne, UK GENE THERAPY PARADIGMS 3 to halt or reverse disease progression in inherited ‘ NIHR Biomedical Research fi Gene therapy is a priori perfectly suited for single Centre at Moorfields Eye neurodegenerative diseases. This eld of research covers gene’ neurological disorders, but some additional Hospital and UCL Institute of a vast area and only the most promising treatment criteria need to be fulfilled, namely: (1) there must Ophthalmology, London, UK paradigms will be discussed with a particular focus on be a relatively clear understanding of the pathways inherited eye diseases, which have paved the way for Correspondence to contributing to neuronal loss to ensure selection of Dr Patrick Yu-Wai-Man, innovative gene therapy paradigms, and mitochondrial the most appropriate therapeutic strategy; (2) the Wellcome Trust Centre for diseases, which are currently generating a lot of debate natural history of the disease must be clearly Mitochondrial Research, centred on the bioethics of germline manipulation.
    [Show full text]
  • Job Description and Person Specificationselection Criteria
    West Wing, Level 6, John Radcliffe Hospital, Oxford, OX3 9DU Web: www.ndcn.ox.ac.uk | Tel: +44(0)1865 234702 | Email: [email protected] Job description and selection criteria Research Technician in Retinal Gene Therapy and Innate Job title Immunity Division Medical Sciences Department Nuffield Department of Clinical Neurosciences Location John Radcliffe Hospital, Headington, Oxford, OX3 9DU Grade and salary Grade 5: £24,298 - £28,982 p.a. Hours Full time – 36.5 hours per week Fixed-term for 1 year in the first instance, with possibility for Contract type extension Reporting to Kanmin Xue (Academic Clinical Lecturer in Ophthalmology) Vacancy reference 121235 Introduction The University The University of Oxford is a complex and stimulating organisation, which enjoys an international reputation as a world-class centre of excellence in research and teaching. It employs over 11,000 staff and has a student population of over 22,000. Our annual income in 2013/14 was £1,174.4m. Oxford is one of Europe's most innovative and entrepreneurial universities: income from external research contracts exceeds £478.3m p.a., and more than 80 spin-off companies have been created. For more information please visit www.ox.ac.uk/about Medical Sciences Division The Medical Sciences Division is an internationally recognized centre of excellence for biomedical and clinical research and teaching, and the largest academic division in the University of Oxford. World-leading programmes, housed in state-of-the-art facilities, cover the full range of scientific endeavour from the molecule to the population. With our NHS partners we also foster the highest possible standards in patient care.
    [Show full text]
  • Research Funding Provided by Choroideremia Research Foundation Curechm.Org
    Research Funding provided by Choroideremia Research Foundation CureCHM.org Funded Researcher Name Institution Project Title USD $ Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2002 Nova Medical School, University of Lisbon, Portugal Choroideremia Research Lab Supplies 1,500 Diseases Research Center Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2003 Nova Medical School, University of Lisbon, Portugal Development of CHM Mouse Model 14,500 Diseases Research Center Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2004 Nova Medical School, University of Lisbon, Portugal Generation of CHM Viral Vector, pt. 1 20,550 Diseases Research Center 2005 Kirill Alexandrov, PhD Max Planck Institute, Germany Forced Expression of REP2 to the Retina 13,000 Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2005 Nova Medical School, University of Lisbon, Portugal Generation of CHM Viral Vector, pt. 2 50,000 Diseases Research Center Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2006 Nova Medical School, University of Lisbon, Portugal Preclinical Gene Therapy Study Year 1 80,460 Diseases Research Center Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2007 Nova Medical School, University of Lisbon, Portugal Preclinical Gene Therapy Study Year 2 69,880 Diseases Research Center Jean Bennett, MD, PhD, F.M. Kirby Professor of Scheie Eye Institute, Perelman School of Medicine, Mouse Study Testing for Three Viral Vector 2010 100,000 Ophthalmology University of Pennsylvania, Philadelphia, PA Candidates Jean Bennett, MD, PhD, F.M. Kirby Professor of Scheie Eye Institute, Perelman School of Medicine, Alternative In-Vitro Assay to Evaluate Three Viral 2011 75,000 Ophthalmology University of Pennsylvania, Philadelphia, PA Vector Candidates Miguel Seabra, MD, PhD, Professor, CEDOC, Chronic 2011 Nova Medical School, University of Lisbon, Portugal Pre-Clinical Gene Therapy Study Year 3 90,000 Diseases Research Center Jean Bennett, MD, PhD, F.M.
    [Show full text]
  • Syncona Corporate Presentation March 2021
    Syncona Corporate presentation March 2021 synconaltd.com Image Freeline labs, Stevenage Cautionary statement This presentation has been prepared and published solely for informational purposes. Nothing contained in this presentation is intended to constitute an offer, invitation or inducement to engage in an investment activity. In this statement, "presentation" means this document together with any oral presentation, any question or answer session and any written or oral material discussed or distributed during the meeting. In making this presentation available, Syncona Ltd makes no recommendation to purchase, sell or otherwise deal in shares in Syncona Ltd or any other securities or investments and you should neither rely nor act upon, directly or indirectly, any of the information contained in this presentation in respect of such investment activity. This presentation has not been approved by an authorised person or by any supervisory or regulatory authority. This presentation speaks as of its date and the information and opinions it contains are subject to change without notice. Neither Syncona Ltd nor its affiliates, agents, directors, managers and advisers (together “representatives”) are under any obligation to update or keep current the information contained in this presentation. The information and opinions contained in the presentation do not purport to be comprehensive. This presentation has not been independently verified. No representation, warranty or other assurance, express or implied, is or will be made in relation to, and no responsibility is or will be accepted by Syncona Ltd or its representatives as to the accuracy, correctness, fairness or completeness of, the information or opinions contained in this presentation. Syncona Ltd and its representatives accept no liability whatsoever for any loss or damage howsoever arising from any use of this presentation or its content or otherwise arising in connection with it.
    [Show full text]
  • 2016 SMAB Minutes (PDF)
    Minutes of the 2016 Meeting of the Scientific and Medical Advisory Board of Retina International Date: Monday, 2nd May, 2016 Time: 1:00 - 2:30 p.m. Location: Washington State Convention Center, Room 3AB, Seattle WA A) Introduction 1. Greetings - Ms. C. Fasser, President, Retina International 2. Scientific Program Introduction – Drs. Eberhard Zrenner and Joe Hollyfield, co- chairmen, Scientific & Medical Advisory Board B) Scientific Program Clinical Trials: Updates and New Trials 1. Stem cell clinical trial in wet AMD: iPS cell-derived RPE - transplantation for age- related macular degeneration-Dr. Masayo Takahashi 2. Stem cell use in RP-Dr. Henry Klassen 3. Update on long-term consequences of subretinal gene therapy for RPE65-LCA-Dr. Artur V. Cideciyan 4. Valproic Acid (VPA) clinical trial-Dr. David Birch 5. New trial of gene therapy for RPE65 deficiency (LCA2) initiated at Moorfields Eye Hospital, London, UK-Dr.Robin Ali PhD 6. RLBP1 Retinitis Pigmentosa: preparation for clinical trial-Dr. Kali Stasi 7. Choroideremia NightstaRx clinical trial-Dr. Robert MacLaren 8. Ocular gene transfer for human X-linked retinoschisis (XLRS)-Drs. Lisa Wei and Paul A. Sieving 9. Current Status of the achromatopsia CNG3B gene therapy clinical trial-Dr. Dominik Fischer 10. Update on clinical trials for RPE65/LRAT-related inherited retinal degenerations – the QLT Inc retinoid program-Dr. Robert Koenekoop 11. Usher gene therapy clinical trial-Dr. Jose-Alain Sahel 12. Retinal electronic prostheses-Dr. Eberhard Zrenner 13. Pixium retinal implant trial-Dr. Serge Picaud 14. The DRUGSFORD project-Dr. François Paquet-Durand RI 2016 SMAB Minutes pg. 1 C) Retina International Announcements, New Business and Conclusions 1) New Business and Announcements – from the floor 2) Final Comments – Ms.
    [Show full text]
  • Eye Research – an Equal Partner’ 2020
    ‘EYE RESEARCH – AN EQUAL PARTNER’ 2020 Eye Research – an equal partner A Report entitled “Eye Research – an equal partner”, compiled and edited by Julian Jackson, featuring contributions from leading researchers in the UK Julian Jackson - Director, Vision Bridge 17/09/2020 1 ‘EYE RESEARCH – AN EQUAL PARTNER’ 2020 Table of Contents 1.0 Introduction 2.0 Understanding the patterns and processes of disease 2.1 Harnessing Human Diversity to Better Understand and Treat Immune Mediated Ocular Diseases 2.2 The case for ‘basic science’ 2.3 Building a Living Lens to Fight Diseases of the Eye 2.4 Eye Related Research 2.5 Harnessing genetic information to discover what causes myopia 2.6 Challenges and therapeutic opportunities for Age-related Macular Degeneration 2.7 The importance of earlier interventions and alternative treatments 2.8 Major advances in genomic research in ophthalmology 2.9 The pre-Descemet’s layer and its relationship with the trabecular meshwork 2.10 If there is no struggle, there is no progress 2.11 From basic cell biology to ocular disease and new therapies 2.12 Taking care of your eyes – the hidden risk of ionizing radiation 2.13 Partner Diagnostics and Therapeutics for genetic eye disease 2.14 Alternative models for studying complex diseases 2.15 Understanding the role of the immune system in eye disease 2.16 Understanding Biology to Develop Novel Therapies or Molecular Therapies for Ocular Scarring 2.17 Understanding disease mechanisms with post mortem eye disease models 2.18 Understanding response, repair and regeneration
    [Show full text]