WHILE A SMALL NUMBER OF PEOPLE ARE SUFFERING FROM A SINGLE RARE DISEASE, 350 MILLION PEOPLE WORLDWIDE ARE SUFFERING FROM RARE DISEASES.

Similar documents
TRANSFORMING GLOBAL GENETIC DATA INTO MEDICAL DECISIONS

Konica Minolta to Acquire Invicro (US)

COPE. FAQs CORPORATE ONCOLOGY PROGRAM FOR EMPLOYEES

CRO partner in Rx/CDx Co-Development

Maximizing Market Access: THE 5 MOST CRITICAL QUESTIONS TO ASK WHEN LAUNCHING A SPECIALTY DRUGS

Presentation to the Committee on Accelerating Rare Disease Research and Orphan Product Development

Shivom, the global Genomics-Blockchain Ecosystem The Next Era of Genomics and Healthcare

GENE EXPRESSION REAGENTS MARKETS (SAMPLE COPY, NOT FOR RESALE)

Research and development case study. Human health research

New Frontiers in Personalized Medicine

MOSAIQUES DIAGNOSTICS

QIAGEN Sample & Assay Technologies From Discovery to Patient

Future Pharma - Challenges & Trends MES Process & Minds Conference Berlin, Germany, September 2015

The Innovative Medicines Initiative: Building new models of collaborative research across Europe

Rare Diseases: Challenges and Opportunities NIH Perspective

Personalised Healthcare Solutions (PHCS) Excellence for your Biomarker-driven Strategies

UBS Global Life Sciences Conference

PAREXEL GENOMIC MEDICINE SERVICES. Applying genomics to enhance your drug development journey

E2ES to Accelerate Next-Generation Genome Analysis in Clinical Research

BIOCRATES Life Sciences AG Short Company Presentation

TECHNOLOGIES & SERVICES FOR THERAPEUTIC ANTIBODY DEVELOPMENT

Innovative Pharmaceutical Solutions for Discovery Chemistry, Biology and cgmp Manufacturing

Venture Philanthropy Models: The Leukemia & Lymphoma Society's Therapy Acceleration Program. A FasterCures Webinar June 19, 2013

NHS ENGLAND BOARD PAPER

UBS Global Life Sciences Conference

SMEs in IMI2 Calls for Proposals

Genomic Medicine in France

The In Vitro Diagnostic CRO

The importance of regulatory science in a societal and industrial perspective Annual Conference CORS 24 November 2016

ORPHANET s Services for Researchers. Valérie THIBAUDEAU Database Manager Orphanet

SAMPLE. Mexico Orthopedic Prosthetics Market Outlook to Reference Code: GDMECC0156DB. Publication Date: February 2014

Voyager Therapeutics - A Spinout from UMass Gene Therapy and RNAi Technologies

Rare diseases in the 7th EU Framework Programme for Research and Technological Development

Delivering on the promise: the clinical application of new diagnoses and treatments for RD K A T E B U S H B Y N E W C A S T L E U N I V E R S I T Y

The Belgian pharmaceutical industry strengthens its leading European position. Belgian pharma figures 2015, in a European perspective

Comments on Use of Databases for Establishing the Clinical Relevance of Human Genetic Variants

LYSARC, ACADEMIC PARTNER OF LYMPHOMA CLINICAL RESEARCH. EN

The 100,000 Genomes Project Genomics Collaboration Event Finnish Residence

Sirtex Medical Limited

FDA Drug Approval Process Vicki Seyfert-Margolis, Ph.D.

An Automated Pipeline for NGS Testing and Reporting in a Commercial Molecular Pathology Lab: The Genoptix Case

Pharmaceutical Product Development NASDAQ: PPDI. Dan Darazsdi Chief Financial Officer. Credit Suisse Healthcare Conference November 2009

Process Mining HANA Platform and Startup at Celonis

National Foundation for Women Legislators Annual Meeting September 12, 2015 Tara Ryan Vice President, State Government Advocacy

Brazil Gastric Balloon Procedures Outlook to 2020

Industry Academic Collaboration: A Key to Successful Involvement of Patients Early in Clinical Development

Early Phase Education WHITEPAPER. Three major items to consider when moving from preclinical to clinical development

Type of Activity. Universal Activity Number L04-P

Testimony of Christopher Newton-Cheh, MD, MPH Volunteer for the American Heart Association

The Clinical Research Regulatory Process

Germany Tissue Engineered - Skin Substitutes Market Outlook to 2020

Adaptive Design for Medical Device Development

The Yale Open Data Access (YODA) Project: Lessons Learned in Data Sharing

Parallel Scientific Advice- TLV s perspective. Wing Cheng DIA Euromeeting Vienna 26th March 2014

LA RICERCA TELETHON PER LE MALATTIE RARE TELETHON RESEARCH ON RARE DISEASES

How can pharma outsourcing partners overcome the challenges of a rapidly changing industry?

Life Sciences Practice

ESTIMATE THE IMPACT OF TIME SAVINGS ON YOUR DRUG DEVELOPMENT PROGRAM, ASSET VALUE AND FINANCIAL COMPANY PERFORMANCE

First Annual Biomarker Symposium Quest Diagnostics Clinical Trials

Valuing and Licensing Intellectual Property. Richard Williams

Creating Shared Value: Redefining the Role of Business in Society

Handbook. Precautions/warnings: For professional use only. To support clinical diagnosis. Not yet offered in the US. Page 1

BIOTECH IN FRANCE. key info in. points

TOTAL CANCER CARE: CREATING PARTNERSHIPS TO ADDRESS PATIENT NEEDS

Translational Medicine From Discovery to Health

Pharmamarketing - strategic challenges

CHALLENGES OF GLOBAL CLINICAL TRIAL SUPPLY SOURCING SOME SPECIFICS FOR EMERGING MARKETS

A gateway to academic excellence for Biotech and Pharma

Department of Neurology. MRC Centre for Translational Research in Neuromuscular Diseases Second Scientific Advisory Board Review 21 st November 2011

KINGSMANN CARE GROUP

REIMAGINING DRUG DEVELOPMENT:

Apollo Research and Innovations(ARI) Spearheading Healthcare Research and Innovations for Apollo Hospitals

To Our Shareholders: Reaching Patients with PNH and ahus

ACCELERATING GENOMIC ANALYSIS ON THE CLOUD. Enabling the PanCancer Analysis of Whole Genomes (PCAWG) consortia to analyze thousands of genomes

Enabling Precision Medicine: The Role of Genetics in Clinical Drug Development A Workshop

Genomic Data Is Going Google. Ask Bigger Biological Questions

Grupo Fleury: history, market and strategic positioning, future. Mr. Carlos Marinelli Chief Executive Officer

Integrated Radiology & Pathology Diagnostic Services: The Time is Now at UCLA

4th ANTWERP BIOPHARM DAY SAFETY & EFFICACY CLINICAL TRIALS SOLUTIONS DATE: OCTOBER 29, 2015

Personalized. Health in Canada

Maximizing opportunities towards achieving clinical success D R U G D I S C O V E R Y. Report Price Publication date

Collaborative Development Financing

Greenwood Genetic Center

CFO meets M&A: Value creation in the digital age The Dbriefs Driving Enterprise Value series

Next Generation Sequencing (NGS) Market Size, Growth and Trends ( )

Circle 5: Innovations in Dermatology and Clinical Trials

On Helix. 02 July Harren Jhoti President & CEO

MARCH 15-16, 2018 PARIS PALAIS BRONGNIART. An event of PROGRAM

Helping unlock growth opportunities worldwide

Spark Therapeutics, Inc. (Exact Name of Registrant as Specified in its Charter)

The future of PMS in Healthcare IT: Announcing the cooperation with Epic. Stan Smits CEO Medical IT Philips Medical Systems

Quintiles Transnational Corporation Big is Beautiful

Akers Biosciences, Inc. Screening and testing technologies that deliver rapid health information to consumers and healthcare providers

France Pressure Relief Devices Market Outlook to 2020

Post-doctoral PharmD Fellowship Programs

QuantStudio Dx Real-Time PCR Instrument

Transcription:

June 2017

WHILE A SMALL NUMBER OF PEOPLE ARE SUFFERING FROM A SINGLE RARE DISEASE, 350 MILLION PEOPLE WORLDWIDE ARE SUFFERING FROM RARE DISEASES. 3rd most populous country 50% of affected are children 30% will not see their 5th birthday 7.6 years to diagnose in US 80% OF RARE DISEASES ARE CAUSED BY MUTATIONS IN OUR GENOME.

RARE DISEASE COMPANY As one of the largest and most diversified genetic testing companies we are dedicated to transforming the worldwide science of genetic data into solutions and hope for patients and their families by answering two very important questions. 1. How to identify patients with a specific rare disease as early as possible? 2. What is the best treatment for these patients?

CENTOGENE Management CEO and CFO Prof. Arndt Rolfs, MD CEO, Founder Professor for Neurology, University of Rostock Consultant for international biotech and industrial companies Principal investigator of multiple international multicenter studies in the area of rare diseases > 220 peer-reviewed papers Richard Stoffelen CFO Certified Public Accountant Nearly 20 years of experience in Big 4 Accounting firm Head of Internal Audit at Holcim Group Services Experienced in IPOs and Bond issuances

CENTOGENE HIGHLIGHTS Established Global Footprint with Strong Historical Growth Growth 2010-2016 by revenue (CAGR): > 40% Headquarters Germany Affiliations Delhi, Dubai, Vienna Cumulative Revenue > EUR 100 mill Outstanding historical growth In EUR million Receiving samples from over 110 countries

CENTOGENE HIGHLIGHTS Building the Definite Knowledge Base in Rare Disease ~ 300 employees Clients: > 16,000 Number of test in 2016 ~120,000 Academics employed: ~70% CentoMD Identified Individuals: ~120,000 Number of Genes in the Test Portfolio: >3,100

CENTOGENE s Business Model A self-amplifying value cycle building the Definite Knowledge Base in Rare Disease Knowledge Products Diagnostic s Pharma Collaborations Data, Information, Knowledge

Diagnostics The Foundation of Genetic Information and Entrance to Higher Value Added Solutions Knowledge Products Diagnostics Pharma Collaborations Samples Collection Sequencing Bioinformatics & Interpretation Medical Report Creation

CentoCard and CentoPortal Simple-to-use Logistics solution to Physicians and Patients SENDING SAMPLES AS POSTCARDS ORDER AND ACCESS TEST REPORTS AT ANY TIME FROM ANYWHERE

Pharmaceutical Collaborations High margin solutions monetized gained from Diagnostics services Knowledge Products Diagnostics Pharma Collaborations Data Knowledge CENTOGENE s is able to translate its Strengths into the needs of Pharmceutical companies and CROs by assisting them to: Patients screening and finding Clincial trails and marketable phases Biomarker development Trial design and planning Support clinical trial phases Companion Diagnostics Precision medicine supporting reimbusement Increase rare disease awareness from collaborational partnership and co-marketing efforts

EXAMPLES of BIOMARKER DEVELOPMENT at CENTOGENE

Knowledge Products Connecting knowledge between genotype and phenotype Knowledge Data Knowledge Products Diagnostics Pharma Collaborations Genetic Variants Clinical Symptoms Knowledge Data

CentoMD 3.3 - LARGEST MUTATION DATABASE FOF RARE DISEASES, FULLY CURATED, BASED ON CLINICAL AND GENETIC DATA CentoMD is our proof-of-concept for digital products that meet FDA s medical device regulation > 3,300 > 790 Mio > 4.0 Mio Centogene is a world-wide first mover in FDA-approved medical databases Genotype-Phenotype Phenotype-Genotype

CentoCloud offering Unique High Quality Bioinformatic Services Preparation Sequencing Processing Interpretation Communication Sequencing Billing Customer Customer Panel design & generation Sequencing Bioinformatic pipeline Technical & medical interpretation Creating medical report

CENTOGENE Accelerated growth by combination of new technologies

OUR BUSINESS MODEL IS SELF AMPLIFYING EVERY STEP OF THE WAY

THANK YOU