ACCELERATING THE DEVELOPMENT
OF NEW DRUGS AND DIAGNOSTICS
MAXIMIZING THE IMPACT OF THE
CURES ACCELERATION NETWORK
Workshop Summary
Steve Olson and Anne B. Claiborne, Rapporteurs
Forum on Drug Discovery, Development, and Translation
Board on Health Sciences Policy
INSTITUTE OF MEDICINE
OF THE NATIONAL ACADEMIES
THE NATIONAL ACADEMIES PRESS
Washington, D.C.
www.nap.edu
THE NATIONAL ACADEMIES PRESS 500 Fifth Street, NW Washington, DC 20001
NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engineering, and the Institute of Medicine.
This study was supported by contracts between the National Academy of Sciences and Department of Health and Human Services (Contract Nos. N01-OD-4-2139 and HHSF223001003T), Abbott Pharmaceuticals, American Diabetes Association, American Society for Microbiology, Amgen Inc., Association of American Medical Colleges, Bristol-Myers Squibb, Burroughs Wellcome Fund, Celtic Therapeutics, LLLP, Critical Path Institute, Doris Duke Charitable Foundation, Eli Lilly & Co., FasterCures, Foundation for the NIH, Friends of Cancer Research, GlaxoSmithKline, Janssen Research & Development, LLC, March of Dimes Foundation, Merck & Co., Inc., Novartis Pharmaceuticals Corporation, and Pfizer Inc. The views presented in this publication do not necessarily reflect the views of the organizations or agencies that provided support for the project.
International Standard Book Number-13: 978-0-309-26116-6
International Standard Book Number-10: 0-309-26116-3
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Copyright 2012 by the National Academy of Sciences. All rights reserved.
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Suggested citation: IOM (Institute of Medicine). 2012. Accelerating the Development of New Drugs and Diagnostics: Maximizing the Impact of the Cures Acceleration Network: Workshop Summary. Washington, DC: The National Academies Press.
“Knowing is not enough; we must apply.
Willing is not enough; we must do.”
—Goethe
INSTITUTE OF MEDICINE
OF THE NATIONAL ACADEMIES
Advising the Nation. Improving Health.
THE NATIONAL ACADEMIES
Advisers to the Nation on Science, Engineering, and Medicine
The National Academy of Sciences is a private, nonprofit, self-perpetuating society of distinguished scholars engaged in scientific and engineering research, dedicated to the furtherance of science and technology and to their use for the general welfare. Upon the authority of the charter granted to it by the Congress in 1863, the Academy has a mandate that requires it to advise the federal government on scientific and technical matters. Dr. Ralph J. Cicerone is president of the National Academy of Sciences.
The National Academy of Engineering was established in 1964, under the charter of the National Academy of Sciences, as a parallel organization of outstanding engineers. It is autonomous in its administration and in the selection of its members, sharing with the National Academy of Sciences the responsibility for advising the federal government. The National Academy of Engineering also sponsors engineering programs aimed at meeting national needs, encourages education and research, and recognizes the superior achievements of engineers. Dr. Charles M. Vest is president of the National Academy of Engineering.
The Institute of Medicine was established in 1970 by the National Academy of Sciences to secure the services of eminent members of appropriate professions in the examination of policy matters pertaining to the health of the public. The Institute acts under the responsibility given to the National Academy of Sciences by its congressional charter to be an adviser to the federal government and, upon its own initiative, to identify issues of medical care, research, and education. Dr. Harvey V. Fineberg is president of the Institute of Medicine.
The National Research Council was organized by the National Academy of Sciences in 1916 to associate the broad community of science and technology with the Academy’s purposes of furthering knowledge and advising the federal government. Functioning in accordance with general policies determined by the Academy, the Council has become the principal operating agency of both the National Academy of Sciences and the National Academy of Engineering in providing services to the government, the public, and the scientific and engineering communities. The Council is administered jointly by both Academies and the Institute of Medicine. Dr. Ralph J. Cicerone and Dr. Charles M. Vest are chair and vice chair, respectively, of the National Research Council.
PLANNING COMMITTEE FOR THE WORKSHOP ON MAXIMIZING THE GOALS OF THE CURES ACCELERATION NETWORK TO ACCELERATE THE DEVELOPMENT OF NEW DRUGS AND DIAGNOSTICS1
CAROLYN COMPTON (Co-Chair), Critical Path Institute, Tucson, AZ
LOUIS J. DEGENNARO (Co-Chair), the Leukemia & Lymphoma Society, White Plains, NY
MARGARET ANDERSON, FasterCures, Washington, DC
ANN BONHAM, Association of American Medical Colleges, Washington, DC
C. THOMAS CASKEY, Baylor College of Medicine, Houston, TX
WILLIAM W. CHIN, Harvard Medical School, Boston, MA
PETER B. CORR, Celtic Therapeutics, LLLP, New York, NY
PAUL R. EISENBERG, Amgen Inc., Thousand Oaks, CA
KATHY L. HUDSON, National Institutes of Health, Bethesda, MD
ANKIT MAHADEVIA, Atlas Venture, Cambridge, MA
ROBERT T. O’NEILL, Food and Drug Administration, Chestnut Hill, MA
BARRY PALLOTTA, Defense Advanced Research Projects Agency, Arlington, VA
MARY K. PENDERGAST, Pendergast Consulting, Washington, DC
ELLEN V. SIGAL, Friends of Cancer Research, Washington, DC
WILLIAM L. WARREN, Sanofi Pasteur, Orlando, FL
IOM Staff
ANNE B. CLAIBORNE, Forum Director
ADRIENNE STITH BUTLER, Senior Program Officer
REBECCA A. ENGLISH, Associate Program Officer
ELIZABETH F. C. TYSON, Research Associate
ROBIN GUYSE, Senior Program Assistant
ANDREW M. POPE, Director, Board on Health Sciences Policy
____________
1 Institute of Medicine planning committees are solely responsible for organizing the workshop, identifying topics, and choosing speakers. The responsibility for the published workshop summary rests with the workshop rapporteurs and the institution.
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FORUM ON DRUG DISCOVERY, DEVELOPMENT, AND TRANSLATION1
JEFFREY M. DRAZEN (Co-Chair), New England Journal of Medicine, Boston, MA
STEVEN K. GALSON (Co-Chair), Amgen Inc., Thousand Oaks, CA
MARGARET ANDERSON, FasterCures, Washington, DC
HUGH AUCHINCLOSS, National Institute of Allergy and Infectious Diseases, Bethesda, MD
LESLIE Z. BENET, University of California, San Francisco
ANN BONHAM, Association of American Medical Colleges, Washington, DC
LINDA BRADY, National Institute of Mental Health, Bethesda, MD
ROBERT CALIFF, Duke University Medical Center, Durham, NC
C. THOMAS CASKEY, Baylor College of Medicine, Houston, TX
GAIL H. CASSELL, Harvard Medical School (Visiting), Carmel, IN
PETER B. CORR, Celtic Therapeutics, LLLP, New York, NY
ANDREW M. DAHLEM, Eli Lilly & Co., Indianapolis, IN
TAMARA DARSOW, American Diabetes Association, Alexandria, VA
JAMES H. DOROSHOW, National Cancer Institute, Bethesda, MD
GARY L. FILERMAN, Atlas Health Foundation, McLean, VA
GARRET A. FITZGERALD, University of Pennsylvania School of Medicine, Philadelphia
MARK J. GOLDBERGER, Abbott Pharmaceuticals, Rockville, MD
HARRY B. GREENBERG, Stanford University School of Medicine, CA
STEPHEN GROFT, National Center for Advancing Translational Sciences, Bethesda, MD
LYNN HUDSON, Critical Path Institute, Tucson, AZ
THOMAS INSEL, National Center for Advancing Translational Sciences, Bethesda, MD
MICHAEL KATZ, March of Dimes Foundation, White Plains, NY
PETRA KAUFMANN, National Institute of Neurological Disorders and Stroke, Bethesda, MD
JACK D. KEENE, Duke University Medical Center, Durham, NC
RONALD L. KRALL, University of Pennsylvania Center for Bioethics, Steamboat Springs, CO
FREDA LEWIS-HALL, Pfizer Inc., New York, NY
MARK B. McCLELLAN, The Brookings Institution, Washington, DC
CAROL MIMURA, University of California, Berkeley
____________
1 Institute of Medicine forums and roundtables do not issue, review, or approve individual documents. The responsibility for the published workshop summary rests with the workshop rapporteurs and the institution.
ELIZABETH (BETSY) MYERS, Doris Duke Charitable Foundation, New York, NY
JOHN ORLOFF, Novartis Pharmaceuticals Corporation, East Hanover, NJ
AMY PATTERSON, National Institutes of Health, Bethesda, MD
MICHAEL ROSENBLATT, Merck & Co., Inc., Whitehouse Station, NJ
JANET SHOEMAKER, American Society for Microbiology, Washington, DC
ELLEN SIGAL, Friends of Cancer Research, Washington, DC
ELLIOTT SIGAL, Bristol-Myers Squibb, Princeton, NJ
ELLEN R. STRAHLMAN, GlaxoSmithKline, Research Triangle Park, NC
NANCY SUNG, Burroughs Wellcome Fund, Research Triangle Park, NC
JANET TOBIAS, Ikana Media and Mount Sinai School of Medicine, New York, NY
JOANNE WALDSTREICHER, Janssen Research & Development, LLC, Raritan, NJ
JANET WOODCOCK, Food and Drug Administration, White Oak, MD
IOM Staff
ANNE B. CLAIBORNE, Forum Director
RITA S. GUENTHER, Program Officer
REBECCA A. ENGLISH, Associate Program Officer
ELIZABETH F. C. TYSON, Research Associate
ROBIN GUYSE, Senior Program Assistant
ANDREW M. POPE, Director, Board on Health Sciences Policy
Reviewers
This report has been reviewed in draft form by individuals chosen for their diverse perspectives and technical expertise, in accordance with procedures approved by the National Research Council’s Report Review Committee. The purpose of this independent review is to provide candid and critical comments that will assist the institution in making its published report as sound as possible and to ensure that the report meets institutional standards for objectivity, evidence, and responsiveness to the study charge. The review comments and draft manuscript remain confidential to protect the integrity of the process. We wish to thank the following individuals for their review of this report:
Barry S. Coller, The Rockefeller University
Garry A. Neil, Johnson & Johnson
Mary K. Pendergast, Pendergast Consulting
Heather M. Snyder, Alzheimer’s Association
Although the reviewers listed above have provided many constructive comments and suggestions, they did not see the final draft of the report before its release. The review of this report was overseen by Brian L. Strom, University of Pennsylvania Perelman School of Medicine. Appointed by the Institute of Medicine, he was responsible for making certain that an independent examination of this report was carried out in accordance with institutional procedures and that all review comments were carefully considered. Responsibility for the final content of this report rests entirely with the authors and the institution.
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Contents
Overview of the Themes of the Workshop
2 APPROACHES TO ACCELERATING TRANSLATIONAL SCIENCE
Cystic Fibrosis and the Need for Partnerships
Alzheimer’s Disease and the Drug Development Ecosystem
NUT Midline Carcinoma and Open Innovation
Sickle Cell Anemia and the Need for Hedgehogs
Leukemia and Lymphoma and the Need for Partnerships
3 APPLICATION OF MATCHING AUTHORITY
The Small Business Innovation Research Program at the National Cancer Institute
The Matching Requirement at the Cancer Prevention and Research Institute of Texas
The Matching Requirement at the California Institute for Regenerative Medicine
4 APPLICATION OF FLEXIBLE RESEARCH AUTHORITY
ARPA-E at the Department of Energy
Promoting an Effective Medical Countermeasures Enterprise at BARDA
Collaboration at the CHDI Foundation
5 SITUATING CAN WITHIN THE DRUG DEVELOPMENT ECOSYSTEM
The Office of Science and Technology Policy
6 FINAL REFLECTIONS ON WAYS TO MAXIMIZE THE GOALS OF CAN
Changing the Culture and Showing Deliverables
“The Status Quo Is Not Acceptable”
B PUBLIC HEALTH SERVICE ACT, TITLE IV—NATIONAL INSTITUTES OF HEALTH
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AHRQ | Agency for Healthcare Research and Quality |
ARPA-E | Advanced Research Projects Agency—Energy |
BARDA | Biomedical Advanced Research and Development Authority |
CAN | Cures Acceleration Network |
CBRN | chemical, biological, radiological, and nuclear |
CDC | U.S. Centers for Disease Control and Prevention |
CDER | Center for Drug Evaluation and Research |
CDRH | Center for Devices and Radiological Health |
CIRM | California Institute for Regenerative Medicine |
C-Path | Critical Path Institute |
CPRIT | Cancer Prevention and Research Institute of Texas |
CTSA | Clinical and Translational Science Award |
DARPA | Defense Advanced Research Projects Agency |
DoD | Department of Defense |
DTRA | Defense Threat Reduction Agency |
EUA | emergency use authorization |
FAR | Federal Acquisition Regulation |
FDA | U.S. Food and Drug Administration |
FNIH | Foundation for the NIH |
IND | Investigational New Drug |
IOM | Institute of Medicine |
LLS | Leukemia & Lymphoma Society |
NCATS | National Center for Advancing Translational Sciences |
NCI | National Cancer Institute |
NIH | National Institutes of Health |
OTA | other transaction authority |
PCORI | Patient-Centered Outcomes Research Institute |
SBIR | Small Business Innovation Research |
STTR | Small Business Technology Transfer |
TAP | Therapy Acceleration Program |
TIA | Technology Investment Agreement |