Friedreich Ataxia Friedreich Ataxia Research Association Australasia.

Slides:



Advertisements
Similar presentations
NIHR Delivering Better Health 20 November 2012, Leeds Dr David Cox Deputy Director – Research Finance & Programmes.
Advertisements

Discovery: Stem Cell Biology NIH Actions Continue infrastructure award program Characterize cell lines Stimulate more research on basic biology Train.
SPANISH ASSOCIATION OF ATAXIA PATIENTS FEDAES  In 1998, we generated the ing list of Hispataxia and the webpage.  In 2000, we contacted researchers.
Ataxia research update Ataxia Ireland conference 28 Sep 2013 Dr Alison Stevenson.
Pathway to Clinical Trials Jennifer Farmer, MS, CGC Coordinator, Collaborative Clinical Research Network in FA Executive Director, FARA (484)
Glaucoma Research Boosting optic nerve energy to slow glaucoma Ian Trounce Principal Investigator CERA Wagstaff Fellow RVEEH.
PRoBaND Parkinson’s Repository of Biosamples and Networked Datasets History Hypotheses Overview Linkage to other studies Funded by Parkinson’s UK Dr Donald.
Influencing Change in Research, Treatment Protocols, and New Drug Development.
Biochemical Mechanisms in Friedreich Ataxia Robert B. Wilson, M.D., Ph.D. Friedreich’s Ataxia Symposium 14 November 2009.
Michael Birrer, PI, Director, Gynecologic Medical Oncology, MGH Lari Wenzel, Co-PI, Prof. of Medicine, University of California, Irvine
Tay-sachs Disease Yi Cheng Lisa Nguyen.
Embryonic Stem Cell Research: Debate and Controversy Leigh Kemp.
Therapeutics for the Muscular Dystrophies.  Mission  Increase the longevity and quality of life of patients with muscular dystrophy  Lead Drug Candidate.
By Robert Johnson SPINAL MUSCULAR ATROPHY. SYMPTOMS INFANT Can have a breathing difficulty Difficulty feeding, food may go down windpipe instead of stomach.
HIV Clinical Trials Janice Price, M.Ed, RN HIV Clinical Research Program Coordinator Swedish Medical Center Seattle, WA USA.
Helena Chui, M.D. McCarron Professor and Chair of Neurology Director, Alzheimer Disease Research Center.
New Employee Orientation
New Employee Orientation (Insert name) County Health Department.
Development of the International Stem Cell Registry: Progress and Challenges.
Accessing the Accelerated Approval Pathway with a Rare Neurologic Disease Batten Disease June 29-30, 2010 FDA Public Meeting “Considerations regarding.
Cardiac Issues in Friedreich’s Ataxia 2 nd Annual Friedreich’s Ataxia Symposium Robert E. Shaddy, MD Jennifer Terker Professor of Pediatrics Division Chief,
Introduction to stem cells Stem cell Community Forum Raymond Wong, PhD Neuroregeneration Research Unit, CERA.
Centers of Excellence Monterey Bay Public Employees Trust Centers of Excellence 2014 Centers of Excellence are selected after careful review by.
Welcome to the Fall 2010 TBPT Meeting Dr. Paul Klotman President and CEO Baylor College of Medicine November 3, 2010.
A one year audit of achieving patient driven performance targets in a locally provided memory clinic Dr C Crowe, St Patrick’s Hospital, Cashel & St Michael’s.
Help build a research resource for scientists studying Congenital Muscular Dystrophy.
Supporting research and patient outreach for FacioScapuloHumeral Muscular Dystrophy (FSHD), one of the most common forms of muscular dystrophy. Progress.
FTD Family Members Study & Post Mortem Study Alyson Negreira MGH Frontotemporal Disorders Unit.
ASH SPECIALIST PROGRAM REPORT Thomas D. Giles, MD, President of the ASH Specialist Program Inc.,
The National Children’s Study A Very Brief History Spring 2000 – Interagency Coordinating Committee established October 2000 – Children’s Health Act authorizes.
Cancer in Our Genes International Patient Database A patient-driven database dedicated to finding a cure for VHL and other cancers.
Testing People Scientifically.  Clinical trials are research studies in which people help doctors and researchers find ways to improve health care. Each.
European Regenerative Medicine Firms & Their Strategic Approaches Michael Morrison University of York.
DEEP Project presentation 03/03/2014 – Caltanissetta Donato Bonifazi – DEEP2 Trial Leader Aurelio Maggio – Trial Coordinating Investigator Lorella Pitrolo.
Investigation of Possible Periodic Paralysis (P3)
NCI Review of the Clinical Trials Process 6 th Annual National Forum on Biomedical Imaging in Oncology James H. Doroshow M.D. April 7, 2005 Bethesda, Maryland.
1 (IPC) Alan Menter Florence, Italy November 19, 2004 The International Psoriasis Council.
HEREDITARY ATAXIA ZEESHAN GAUHAR PhD SCHOLOR-BIOTECHNOLOGY
Long Term Follow Up of Subjects in Gene Transfer Clinical Trials Philippe Bishop, MD FDA/CBER Division of Clinical Trial Design and Analysis Oncology Branch.
Opportunities and Obstacles in Genetic Counseling Training: The Philippines’ Experience Mercy Laurino, MS CGC Licensed Genetic Counselor November 2, 2011.
Experimental Gene Therapy Use On Humans. What is gene therapy? Gene therapy is a method of curing genetic disorders by introducing functioning genes into.
+ National and Institutional Guidelines on Conflict of Interest in Physician-Industry Relationships.
Mental Health Services and Autism Spectrum Disorders Ann M. Neumeyer, MD Medical Director, Lurie Center / LADDERS Associate Pediatrician and Neurologist.
1 Safety of Cell Therapies Derived from Human Embryonic Stem Cells CTGTAC #45 April 10, 2008.
Advances in Stem Cell Therapy Karim Nayernia Professor of Human Genetics & Stem Cell Biology.
Site Management Organization (SMO) Making Clinical Trials More Efficient.
The Wisconsin Network for Health Research (WiNHR): Overview. An Infrastructure for Conducting Multi-Site Clinical Research across the State of Wisconsin.
Plenary III: There is No Health Without Mental Health.
Understanding Genetic Testing
Access to drugs, Reducing bottlenecks Matt Cooper Business Development & Marketing Director NIHR Clinical Research Network
Huntington's Disease By: Walter Gerring and Seth Little.
Kathleen Giacomini, Mark J. Ratain, Michiaki Kubo, Naoyuki Kamatani, and Yusuke Nakamura NIH Pharmacogenomics Research Network III & RIKEN Center for Genomic.
Research in the Office of Cellular, Tissue and Gene Therapies: Vision and Overview Jesse Goodman, M.D., M.P.H. Director, Center for Biologics Evaluation.
AUSTRALIAN SCIENTISTS Natalie Sarkez Year 12 Biology.
Usher Syndrome By Andy Beer. What is Usher Syndrome Usher Syndrome is a genetic disease on witch you lose the ability to hear and see. The major symptoms.
Using Australian Clinical Sites – Challenges for International Sponsors Prof A J (Tony) Webber Clinical Network Services Pty Ltd Brisbane, Australia.
Making Clinical Trials More Efficient Site Management Organization (SMO)
M ax D elbrück L ecture Date:June 17th, 2008 Speaker: Kenneth R. Chien MGH Cardiovascular Research Center Boston, USA Title:Toward human models of human.
AHUS Alliance aHUS Global Poll Featuring Analysis & Commentary by Dr. Christoph Licht 21 June 2016 WEBINAR Hosted by RareConnect.
FDA Orphan Products Natural History Grants Program An Opportunity for APBD? Harrison N. Jones, PhD Associate Professor Department of Surgery Duke University.
Stem Cells: Scientific Potential and Alternatives
Ann Intern Med. 2011;155(2): doi: / Figure Legend:
Usher syndrome By Andy Beer.
The Essentia Institute of Rural Health (EIRH) is
Dr Charlotte Lemech Medical Director, Scientia Clinical Research
Clinical Trials in IBD.
Physician / Patient Future Collaboration Opportunities
Gene Therapy: Past, Present, and Future
Nat. Rev. Nephrol. doi: /nrneph
Friedreich’s Ataxia.
Presentation transcript:

Friedreich Ataxia Friedreich Ataxia Research Association Australasia

What is Friedreich Ataxia? Most common form of hereditary ataxia Autosomal recessive disease Caused by a defect in a gene labeled FXN. Both male and female children can inherit the disorder. Age of onset 5 – 15 years 1 in 30,000 in Australia 1 in 90 are carriers Currently no treatment

Brief History 1863 – Friedreich Ataxia first described by Nikolaus Friedreich, a German physician – no Australian research being conducted – gene discovered by Massimo Pandolfo – Professor Bob Williamson appointed Director of Murdoch Institute in Melbourne

FARA(A) – Friedreich Ataxia Research Association (Australasia) Formed in 2003 by Peter Rousch, Mike Dwyer and Steve Beetham Board comprises 6 parents of 10 FA kids. Scientific Advisory Committee: Professor Bronya Keats, Professor Bob Williamson, Professor Kathy North, Professor Ed Byrne, Dr Elizabeth Coulson.

Friedreich Ataxia Clinic First dedicated FA clinic in the world. Held one afternoon per month, free of charge for patients. They can visit with all the relevant FA specialists in the one location. Neurologist, geneticist, physiotherapist, occupational therapist, opthalmologist, cardiologist, etc.

Research we fund Clinical care: Friedreich Ataxia Clinic, Melbourne and Brisbane. Clinical studies: MFARP – Murdoch Friedreich Ataxia Research Program. Neurological, cardiac, speech, kinematic, vision and ocular motility, functional MRI, audiology, quality of life, sexual function and gait studies. Gene therapy: Developing lentiviral vectors for gene therapy of FA Stem Cells: Generation of induced pluripotent stem cells from FA patients; Investigating the cardiac differentiation of FA iPS cells; Generation of sensory nerves from FA iPS cell lines

International FA research AustralasiaUnited States United Kingdom and Europe

Our International Resources FA mouse models banked at JAX – standardized characterization following recommendations of FA international mouse models task force FA iPS neural and cardiac cell lines - banking High Throughput Screening assays FA Collaborative Clinical Research Network (CCRN in FA) FA Data & Clinical Trial Coordination Core FA national and international clinic network FA national and international patient database FA autopsy and tissue donation program for research FA international patient advocacy groups network – USA, Australia, UK, Europe FA international stem cell advisory committee

CCRN in FA Collaborative Clinical Research Network in FA 11 centers worldwide More than 550 patients participate in clinical research and receive medical care at these sites. Includes data coordination and management, a bio-repository, clinical research studies and direct costs for the centers.

Clinical trials Idebenone – completion of Phase III and 6 month extension both in US and Europe. Deferiprone – the Phase II trial of the iron chelator is complete. Pioglitazone – A Phase II/III trial is under way in France and is scheduled for completion in Carbamylated EPO (CEPO) – completion of the Phase II clinical trial in Europe is scheduled before May. A0001 – Phase II trial completed end of December. HDAC inhibitor – currently with the FDA seeking Phase I approval Resveratrol – recruitment has commenced in Melbourne

Stem Cells Annual international FA stem cell meeting International FA Stem Cell Advisory committee Areas of focus – cardiac, neuronal and diabetes Areas of research interest: Neural – peripheral nerve regeneration Cardiac – cardiac tissue engineering Pancreas – diabetes tissue engineering

CAMRA – Coalition for the Advancement of Medical Research Australia NAA – Neurological Alliance Australia ANN – Australian Neuromuscular Network