The Value of Tissue Banks to Drug and Dx Developers Barbara L. Handelin, Ph.D. Conflicts of Interest, Privacy/Confidentiality, and Tissue Repositories:

Slides:



Advertisements
Similar presentations
The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects.
Advertisements

PERSONALIZED MEDICINE. What is Personalized Medicine? Information-based healthcare –Person-by-person: high content, resolution & fidelity –Ushered in.
Personalized Medicine in California Kathryn Lowell, Deputy Secretary for Life Sciences and Health Systems February, 2009.
TISSUE BANKING Challenging to Say the Least
Understanding Genome-Wide Profiling of Cancer
1. 2 Key Applications of Genetic and Genomic Testing (slide 1 of 2) Diagnosis of Disease: Whereby genetic or genomic tests are used to screen a patient.
The Institutional Review Board. What is an IRB? An IRB is committee set up by an institution to review, approve, and regulate research conducted under.
Methods repositories use to protect subjects Roger Aamodt, Ph.D. Resources Development Branch, National Cancer Institute.
Alexandra K. Glazier, JD, MPH Why Gift Law Matters: The Law and Ethics of Donor Designation Next Speaker: Sponsored by.
COOL THINGS ABOUT THE GENOME Humans have fewer genes than expected Human genes make more proteins than those of other critters Humans have adopted 200.
Pharmacogenomics in Japan Hiroshi Gushima Scientific Advisor BioFrontier Partners, Inc. and Yamanouchi Pharmaceutical Co., Ltd. October 3, 2002 The 3rd.
EHealth Unit FP6 - 1st IST Call for Proposals 28/1/2003 The eHealth Strategic Objective Julian Ellis eHealth Unit, DG Information Society
IRB 101: Informed Consent Columbia University Medical Center IRB September 22, 2005.
The Pursuit of Better Medicines through Genetic Research Terri Arledge, DVM US Department Head Drug Development Genetics.
Pharmacogenomics in Drug Development FDA Science Board April 9, 2003 Brian B. Spear, Ph.D. Director, Pharmacogenomics Abbott Laboratories.
8 Criteria for IRB Approval of Research 45 CFR (a)
© NuAge Vision Webwww.nuage-vision.com Tel:+44 (0) (0) Developing.
Clinical Trials The Way We Make Progress Against Disease.
University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director.
Good Clinical Practice GCP
Opportunities for Big Data in Medical Records Mike Conlon, PhD
Human Research Protection Programs 1a: How to Navigate Human Subject Protection Regulations Sponsored by the American Society for Investigative Pathology.
Idara C.E.. Three ethical principles guides research with human participants. principle of Autonomy 1. The principle of Autonomy requires investigators.
Integrating Scientific Advances into Regulation: Pharmacogenomics and Pharmacogenetics Janet Woodcock, M.D. Director, Center for Drug Evaluation and Research.
Treuman Katz Center for Pediatric Bioethics Conference Banking Biological Samples for Pediatric Research Jeffrey R. Botkin, M.D., M.P.H. Professor.
The use of human biospecimens in cancer research Christopher A. Moskaluk M.D., Ph.D. University of Virginia.
A PPP managed by FNIH Partners are NIH, FDA, CMS, and private industry Barbara B. Mittleman, M.D. Director, NIH PPP Program Bioinformatics Forum March.
INTRODUCTION TO RA.
Precision Medicine A New Initiative. The Concept of Precision Medicine (PM) The prevention and treatment strategies that take individual variability into.
Integrated Biomedical Information for Better Health Workprogramme Call 4 IST Conference- Networking Session.
©2004 McDermott, Will & Emery. All Rights Reserved. BST Perspectives From Those Who Regulate Tissue Banks: The Moderator’s Perspective Stephen.
Institutional Review Board (IRB) What is our Purpose and Role for Ethical Research.
TERRENCE F. ACKERMAN, PH.D. PROFESSOR OF BIOETHICS CHAIR, UTHSC IRB.
Gene Expression Signatures for Prognosis in NSCLC, Coupled with Signatures of Oncogenic Pathway Deregulation, Provide a Novel Approach for Selection of.
Sample to Insight Alexander Kaplun, PhD Sep PGMD: a comprehensive pharmacogenomic database for personalized medicine and drug discovery.
Developing medicines for the future and why it is challenging Angela Milne.
Personalized Medicine Dr. M. Jawad Hassan. Personalized Medicine Human Genome and SNPs What is personalized medicine? Pharmacogenetics Case study – warfarin.
The Use of Predictive Biomarkers in Clinical Trial Design Richard Simon, D.Sc. Chief, Biometric Research Branch National Cancer Institute
Rachel Liao, PhD Coordinator of the Clinical Working Group and the BRCA Challenge demonstration project for the Global Alliance for Genomics and Health.
Dr Godfrey Grech University of Malta
Trend in diagnostic biochip development Eiichiro Ichiishi, M.D., Ph.D. Department of Internal Medicine International University of Health and Welfare Hospital.
Genomics, Medicine, and Society American College of Radiology May 13, 2003 Francis S. Collins, M.D., Ph.D.
$100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 Terms Clinical Trial Facts.
The Importance of Tissue Banking and Tissue Research Mark E. Sobel, M.D., Ph.D. Executive Officer, American Society for Investigative Pathology
Why Write A Grant? Elaine M. Hylek, MD, MPH Professor of Medicine Associate Director, Education and Training Division BU CTSI Section of General Internal.
D4FF55A0-6B6F BF422A9BA9 Present by: Xiao Chen On December 7, 2015.
Idara C.E.. Three ethical principles guides research with human participants. principle of Autonomy 1. The principle of Autonomy requires investigators.
Integrating Pharmacogenomic Questions Into GCIG Ovarian Cancer Clinical Trials Lori Minasian, MD Chief, Community Oncology and Prevention Trials Research.
Consumer Advocate Perspective Clinical Trials Registration Sharon F. Terry, JAM Sharon F. Terry, JAM President and CEO, Genetic Alliance, Inc. Founding.
Regulatory Guidance for Genetic Testing. Three Specific Areas Laboratory tests Results of genetic testing – Clinical – Research GenomeWide Association.
Human Specimen Repositories Requirements of 21 CFR Parts 50 & 56 PRIM & R May 5, 2004 Sally A. Hojvat, Ph.D. Director of Microbiology Devices Office of.
Full Proposal for the German Cancer Aid Priority Program 'Translational Oncology' (2st call) 2015 Lead Applicants: Prof. Dr. med. Magnus von Knebel Doeberitz.
Human Research Protection Program 101 March 20, 2007 Cincinnati, OH.
Institutional Review Board (IRB) for Human Subject Protections: Working with the IRB Erin A McClure, PhD Department of Psychiatry and Behavioral Sciences.
Origins of Pharmacogenomics. Archibald Garrod In 1902 Garrod characterized the condition of alcaptonuria as one resulting from an absence of the.
Doug Brutlag 2011 The impact of genomics on the future of medicine and health Muhammad Faisal 2015-Arid-3638 PhD(scholar) Biochemistry.
Collaborative Institutional Training Initiative (CITI) citiprogram.org Georgia Institute of Technology.
European Patients’ Academy on Therapeutic Innovation Challenges in Personalised Medicine.
Moiz Bakhiet, MD, PhD, Professor and Chairman
New research areas in personalised medicines
Telephone    Provider of Global Contract Research Services Accelerating Preclinical Research, Drug Discovery.
Biomarkers.
Semantic Web - caBIG Abstract: 21st century biomedical research is driven by massive amounts of data: automated technologies generate hundreds of.
Susan Sonne, PharmD, BCPP Chair, MUSC IRB II
NISCHR Academic Health Science Collaboration Launch
Yale SPORE in Skin Cancer
Biomedical Therapies Foundation Standard 1: Academic Foundation
Streamlining IRB Procedures for Expanded Access
Data Access and Stewardship
Opening an IND: Investigator Perspective
Presentation transcript:

The Value of Tissue Banks to Drug and Dx Developers Barbara L. Handelin, Ph.D. Conflicts of Interest, Privacy/Confidentiality, and Tissue Repositories: Protections, Policies, and Practical Strategies

Tissue Banks for Tx and Dx Developers: What is the need? Basic research: the biological revolution in the medicinal chemical industry Drug targets Molecular diagnostics Biomarkers for clinical research Clinical research: pharmacogenetic/genomic profiling Toxicity Drug responsiveness Rescuing failed drugs PGx will drive the collection and use of stored tissues into common practice involving millions of subjects

What is needed from tissues? DNA: gene, SNP, population association RNA: gene expression array or profiling Proteins: proteomics Cell morphology: pathology

Pharmacogenetics Is…. The influence of genetic traits on the magnitude or type of toxic effects of drugs. The influence of genetic traits on the magnitude or type of therapeutic effects of drugs. A genetic determinant of overall drug response; not a measurement of physiological status! PGenetics: Targeted study of gene variants determining drug response PGenomics: Genome wide study of genetic determinants, including the study of gene expression (requiring RNA as a study material)

FDA Guidance on PGx PGx will “help individualize therapy with the intent of maximizing effectiveness and minimizing risk.” Important “that FDA policy facilitate, not impede, the use of pharmacogenomic tests during drug development and, to the extent possible, encourage open and public sharing of data…on PGx test results.” “most experimental results may not be well enough established to be suitable for regulatory decision making”

“the FDA is encouraging voluntary submission of such data…” “As…field of PGx advances, it is likely (and desirable) that sponsors will begin to use PGx tests to support drug development and/or to guide therapy” FDA Guidance on PGx

Developing tests for marketed drugs Currently available drugs could be targeted to appropriate patients Leads to: Need for archival repositories with clinical records of all drug therapies Need to revisit stored tissues from prior clinical trials (as in original drug trials) Need to attach PGx testing to Phase III/IV studies

BIO perspectives, recommendations Review commensurate with risk; a two tiered review system Research involving intervention or interaction Research using medical records and tissue archives Federalize regulations/laws governing consent, use and retention of tissue to make consistent with all regulations (not State by State)

BIO perspectives, recommendations Subject’s authorization or specification of limitations on permissible uses of data and biological materials must be respected. E.g. Right to withdraw at any time must be honored

Sample PhRMA perspectives on privacy in tissue research Medical information, including genetic information, should have equal protection Researchers must have unrestricted access to anonymized or encrypted patient information Uniform national requirements should govern biomedical research, although individual states should be able to prescribe additional penalties for violations of privacy

Cooperative Groups (such as the Cooperative HumanTissue Network) Ardais GeneLogic International Genomics Consortium IMPATH Integrated Lab Services Example Tissue Repositories

LifeSpan Biosciences Oncotech PathServe The AlphaOne Foundation Genomics Collaborative Duke Center for Human Genetics Cancer centers Example Tissue Repositories

What is an appropriate posture or role for IRBs to take in this arena? IRBs represent the “interests” and welfare of subjects Gifting for the development of better medicine Do me no harm Allow me to understand my risks “Willing suspension of autonomy”? What is risk of NOT suspending autonomy?

How suspension of autonomy may lead to useful discoveries Complex test to profile newly diagnosed women with breast cancer re risk for recurrence. (Genomic Health, Inc.) Genetic risk factor for MI (DeCODE) New drug into development for MI targeted at genetic risk factor for MI (DeCODE/Bayer) New test for responders to Iressa among non-small cell lung cancers

How suspension of autonomy may lead to useful discoveries Collecting DNA for unknown future use: New test in development for response to treatment with statin drugs: personalized medicine (Gennaissance;Abbott Labs)