BIOMARKERS & MOLECULAR TUMOUR CLASSIFICATION FOR NON-GENOTOXIC CARCINOGENESIS



Similar documents
TECHNOLOGIES, PRODUCTS & SERVICES for MOLECULAR DIAGNOSTICS, MDx ABA 298

EBiSC the first European bank for induced pluripotent stem cells

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE S1A. Current Step 4 version

Quality by Design Concept

Pivot Park Screening Centre participates in novel 196 million pan-european drug discovery platform

dixa a data infrastructure for chemical safety Jos Kleinjans Dept of Toxicogenomics Maastricht University

ICH Topic S 1 A The Need for Carcinogenicity Studies of Pharmaceuticals. Step 5

Just the Facts: A Basic Introduction to the Science Underlying NCBI Resources

Ph.D. in Molecular Medicine

Summary of Discussion on Non-clinical Pharmacology Studies on Anticancer Drugs

Harald Isemann. Vienna Brno Olomouc. Research Institute for Molecular Pathology

Clinical Cancer Research: Alternative IRB Models and Enhancing Progress

SMALL BUSINESS INNOVATION RESEARCH (SBIR) SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) GRANT APPLICATIONS

CURRICULUM VITAE GARY MURRAY WILLIAMS, M.D. Washington and Jefferson College, Washington, Pennsylvania. B.A. 1963; Magna Cum Laude

A leader in the development and application of information technology to prevent and treat disease.

Nuevas tecnologías basadas en biomarcadores para oncología

Achieving Regulatory Success: Areas of focus for biotechnology companies. Michael J. Schlosser, PhD, DABT April 21, 2013

Leukemia Drug Pathway Analyzer

M The Nucleus M The Cytoskeleton M Cell Structure and Dynamics

CLINICAL TRIALS SHOULD YOU PARTICIPATE? by Gwen L. Nichols, MD

School of Nursing. Presented by Yvette Conley, PhD

Cancer Genomics: What Does It Mean for You?

Voluntary Genomic Data Submissions at the U.S. FDA

INSERM/ A. Bernheim. Overcoming clinical relapse in multiple myeloma by understanding and targeting the molecular causes of drug resistance

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE E15

Division of Bioinformatics and Biostatistics

ITT Advanced Medical Technologies - A Programmer's Overview

BBSRC TECHNOLOGY STRATEGY: TECHNOLOGIES NEEDED BY RESEARCH KNOWLEDGE PROVIDERS

IMPLEMENTING BIG DATA IN TODAY S HEALTH CARE PRAXIS: A CONUNDRUM TO PATIENTS, CAREGIVERS AND OTHER STAKEHOLDERS - WHAT IS THE VALUE AND WHO PAYS

The Commercialization of Technology Concepts into Medical Products

NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES Division of Extramural Research and Training

Name Class Date. Figure Which nucleotide in Figure 13 1 indicates the nucleic acid above is RNA? a. uracil c. cytosine b. guanine d.

2 nd PROCART Forum. October 9th, 2012

Worldwide Collaborations in Molecular Profiling

Fit for Health International Strategy Development Training Innovative Business Solutions and Smart Financing

Drug Safety of Stem Cells and other Novel Therapeutics

Human Genome Organization: An Update. Genome Organization: An Update

CANCER RESEARCH UK STRATIFIED MEDICINE PROGRAMME IAN WALKER PHD, MBA HEAD OF STRATIFIED MEDICINE

Pharmacology skills for drug discovery. Why is pharmacology important?

Innovative. Medicines Initiative Call Topics Table of Contents

Session 6 Clinical Trial Assessment Phase I Clinical Trial

ICH M3 (R2) Guideline on Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals

StemCellMathLab Systems Medicine of Leukemia

Guidance for Industry Safety Testing of Drug Metabolites

How Public-Private Partnerships Benefit All Stakeholders Douglas C. Throckmorton, MD Deputy Director for Regulatory Programs, CDER, FDA

Revision of the Directive 98/79/EC on In Vitro Diagnostic Medical Devices. Response from Cancer Research UK to the Commission August 2010

Cancer SBL101. James Gomes School of Biological Sciences Indian Institute of Technology Delhi

Version Module guide. Preliminary document. International Master Program Cardiovascular Science University of Göttingen

Anforderungen der Life-Science Industrie an die Hochschulen. Hans Widmer Novartis Institutes for BioMedical Research

Overview of Phase 1 Oncology Trials of Biologic Therapeutics

Individualizing Your Lung Cancer Care: Informing Decisions Through Biomarker Testing

Non-clinical development of biologics

Building a Collaborative Informatics Platform for Translational Research: Prof. Yike Guo Department of Computing Imperial College London

Why Are Drugs So Expensive? Learning About the Drug Development Process

Epigenetic mechanisms regulate the interpretation of genetic information. Frank Lyko Epigenetics

The National Institute of Genomic Medicine (INMEGEN) was

Nanomedicine in Horizon 2020

Clinical Research Infrastructure at the European level: the ECRIN model. Christine Kubiak ECRIN Coordination Inserm- DRCT

Consortium led by Asbestos Diseases Research Institute (ADRI)

Micromyx. Micromyx. A Microbiology Services Company. Lab Services Research - Consulting -

Systematic Drug Repurposing: Some Successes, Caveats, and Directions

The PROTECT project. Introduction. Xavier Kurz Pharmacovigilance and Risk management Patient Health Protection Unit European Medicines Agency

CAREERS IN BIOMEDICAL SCIENCE

COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) NOTE FOR GUIDANCE ON THE PRE-CLINICAL EVALUATION OF ANTICANCER MEDICINAL PRODUCTS

FSH Society s 2014 Biennial FSHD Connect Meeting: Natural History Studies

PART 3.3: MicroRNA and Cancer

Centre for Biomarker Research in Medicine. COMET Competence Centre for Excellent Technologies

Innovation Platform: Sudden Cardiac Death

Regulatory Issues in Genetic Testing and Targeted Drug Development

Testing Services for Large Molecule Drug Development

Clonetics Conditionally Immortalized Human Cells. Relevant Cells for High Throughput Screening

Department of BioScience Technology Chung Yuan Christian University 2015/08/13

The IMI. to overcome key bottlenecks on the way to novel therapies

MOLOGEN AG German Equity Forum 2015

Exelixis Showcases R&D Pipeline at JPMorgan Healthcare Conference

Euro-BioImaging European Research Infrastructure for Imaging Technologies in Biological and Biomedical Sciences

Roche Position on Human Stem Cells

Attacking the Biobank Bottleneck

Applications of comprehensive clinical genomic analysis in solid tumors: obstacles and opportunities

The Myelin Repair Foundation: Accelerating New Treatments for Multiple Sclerosis and All Diseases. Scott Johnson CEO, President and Founder

The Clinical Trials Process an educated patient s guide

Dr Alexander Henzing

Appendix 2 Molecular Biology Core Curriculum. Websites and Other Resources

Enabling Discovery, Development, and translation of treatments for Cognitive Dysfunctions in Depression: A Workshop Session IV

Basic Overview of Preclinical Toxicology Animal Models

Sommaire projets sélectionnés mesure 29: Soutien à la recherche translationnelle

Navigating England s clinical research infrastructure. How NOCRI helps simplify access to accelerate discoveries

CONTRACTING ORGANIZATION: University of Alabama at Birmingham Birmingham, AL 35294

History and Principles of Good Clinical Practice

DWI Case Study - QIBA PDF- MRI Technical Committee. What is IMI?

An integrated global healthcare company

Genetic testing. The difference diagnostics can make. The British In Vitro Diagnostics Association

BioTalentum Ltd. Hungary Prof. András Dinnyés Director

New Tools. Diseases. for Research on. R&D for Neglected Patients. Scientific Symposium. conference programme. In collaboration with.

2019 Healthcare That Works for All

micrornas Non protein coding, endogenous RNAs of 21-22nt length Evolutionarily conserved

Genetic information (DNA) determines structure of proteins DNA RNA proteins cell structure enzymes control cell chemistry ( metabolism )

WG5: Informatics. Martin Dugas, Jaakko Hollmen. European Genomics and Epigenomics Study on MDS and AML

BIOSKETCH. Degrees: Cand. real. 1971, Dr. philos University of Bergen, Norway

Transcription:

MARCAR BIOMARKERS & MOLECULAR TUMOUR CLASSIFICATION FOR NON-GENOTOXIC CARCINOGENESIS

What patients need What Europe needs Improved drug safety Increased efficiency of drug development Earlier detection of undesired effects of candidate drugs during development MARCAR focus on NON-GENOTOXIC CARCINOGENESIS Identify BIOMARKERS: - help predict cancer risk more accurately at a very early stage - speed up development & increase drug safety for patients

Why focus on Non-Genotoxic Carcinogenesis (NGC)? DNA damage Base alteration Crosslink Abasic site Double strand break Chromosome damage Point mutations Carcinogenesis Multistage process Cancer Pyrimidine dimer Single strand break Genotoxicity testing Required for IND Genetox battery Cost: $60K/cmpd Time: 1-3 month Non-genotoxic mechanisms Nuclear receptor activation Proliferation Epigenetics mirna Methylation Carcinogenicity testing Required for NDA 2-year bioassay Cost:$3M/cmpd Time: 3 years Schematic Figure adapted from Ellinger-Ziegelbauer et al., (2009) Toxicol Lett. (Elsevier) 186:36-44 with authors permission No sufficiently accurate or well-validated short-term assays to identify NGC Need early mechanism-based biomarkers for the design of more predictive tests & improved cancer risk assessment

What we will do MARCAR will search for biological clues (BIOMARKERS) to enable EARLY preclinical DETECTION of drug-induced tumor formation 2 year rodent cancer bioassay supporting clinical development and drug registration IDENTIFY BIOMARKERS USING INNOVATIVE TECHNOLOGIES AND MECHANISTIC MODELS: EPIGENETICS; microrna; BIOINFORMATICS MOUSE MODELS CONTAINING HUMAN GENES IMPORTANT FOR NGC TRANSLATIONAL IN VITRO CELL-BASED MODELS NON-INVASIVE IMAGING & REPORTER MODELS ASSESS PREDICTIVE VALUE OF NOVEL BIOMARKERS & RELEVANCE FOR HUMANS

Emerging importance of epigenetics for cancer biology INITIATION PROMOTION PROGRESSION Clonal expansion Acquired characteristics metastasis, angiogenesis CLASSICAL mutation mutation mutation EMERGING VIEW mutation/ epimutation mutation/ epimutation mutation/ epimutation EPIMUTATIONS: = Paradigm shift in established models for tumour progression 5

EPIGENETIC CODES opportunity to identify novel biomarkers for early cancer detection GENETIC CODE (A,C,T,G) EPIGENETIC CODES 5-methycytosine www.epigenome.eu Epigenome Network of Excellence (NoE) EU Framework 6 Programme (FP6) Luger et al., (1997) Nature 389:251-260

Expected outcomes & benefits to patients Improved scientific basis for risk assessment of carcinogenic potential of novel medicines Novel early biomarkers for more reliably predicting later cancer development Increased efficiency of drug development - fewer delays/attrition during late-phase Improved preclinical safety assessment prior to clinical trials & potential translation of early cancer biomarkers to humans

Added value of consortium New knowledge + biomarkers can be more rapidly derived by sharing consortium expertise, technologies, models, and archives Extensive collection of archived samples and data from preclinical studies (3Rs) Opportunity for continuous regulatory input (via advisory board) on cancer risk assessment & biomarker qualification Access to unique molecular profiling technologies and mechanistic models

Results/achievements New technologies established for monitoring drug-induced perturbation of epigenome and micrornas in rodent tissues (e.g. INTEGRATED GENOME-WIDE MOLECULAR PROFILING) Identification of novel early candidate biomarkers for non-genotoxic carcinogenesis (e.g. NON-CODING RNAs & CANCER SIGNALLING PATHWAYS) Novel insight into human relevance of candidate biomarkers using mouse models (e.g. CAR & PXR NUCLEAR RECEPTORS)

Time and money Financing IMI funding: 6.049.578 EFPIA in kind contribution: 5.155.604 Other contributions: 2.114.051 Total project cost: 13.319.233 Timing: Starting date: 01.01.2010 Duration: 60 months

Participants EFPIA Novartis (Coordinator) UCB Pharma SA Bayer Schering Pharma AG Lundbeck Boehringer Ingelheim SME CXR Biosciences Ltd., UK EMEA & FDA scientists Academic University of Dundee, UK (Managing Entity of fimi beneficiaries) Medizinische Universitat, Vienna, Austria Medical Research Council, Edinburgh, UK Eberhard Karls Universitat, Tubingen, Germany Natural & Medical Sciences Institute, Reutlingen, Germany via ad-hoc advisory board Institut National de la Sante et de la Recherche, Montpellier, France

Further information www.imi-marcar.eu www.imi.europa.eu