We've all heard the dismal statistics: 10,000 known diseases with only 500 treatments. Not great odds if you're a patient.

Similar documents
May 13, Washington, DC Washington, DC Washington, DC Washington, DC 20515

Chairman Cole, Ranking Member DeLauro and distinguished members of the

March 2, Dear Chairman Upton, Ranking Member Pallone, and Representative DeGette:

The 21st Century Cures Act

A Discussion Focused on Right to Try

Welcome to the Duke CTSI Virtual Town Hall

Building a Career in the Pharmaceutical Industry: Personal Reflections. Carlo Nalin, PhD Executive Director Novartis Oncology

social, and population-based research conducted and supported by the National Institutes of Health (NIH). The

The Role of Philanthropy in Medical Device Development

Employment in the biopharma industry grew almost 5 percent in 2014, the last full year for which we have data. This is the highest annual growth rate

Federal Funding for Brain Research. Congressional Support Accelerates Discovery

On behalf of the Cystic Fibrosis Foundation (CFF) and the 30,000 people with cystic

Dear Chairmen Upton and Pitts, Ranking Members Pallone and Green, and Ms. DeGette:

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

Critical Incentive Strategies for Accelerating R&D to Fight Against AMR

FDA Critical Path Initiative: Closing Productivity Gap in Medical Product Development. October 4, 2004

New Drug Application (NDA) Webinar December 6, 2016

2015 Policy Landscape: A Biomedical R&D Planning Guide

Delivering on the Promise of Precision Medicine

Summary of Provisions in 21 st Century Cures Act (H.R. 6) as passed by full House of Representatives, July 10, 2015

Developing Drugs for Rare Diseases: Patient Advocacy s Perspective. Kristina Bowyer Executive Director, Patient Advocacy

FROM PERCEPTION TO MEASURED REALITY. Leverage Analytics to Improve Clinical & Economic Outcomes 1 A 5-MINUTE EXECUTIVE BRIEF FROM ECOLAB HEALTHCARE

Real World Evidence how patient groups can contribute and how to engage patient groups in clinical research

Associate Director of Public Policy, National Organization for Rare Disorders (NORD)

E&T objectives in evolving pharma business models. Magda Chlebus Director Science Policy Brussels, 2 March 2015

PDUFA VI Public Meeting Remarks of Cynthia A. Bens Alliance for Aging Research. August 15, 2016

GE Launches Healthymagination ; Will Commit $6 Billion to Enable Better Health Focusing on Cost, Access and Quality

CRO partner in Rx/CDx Co-Development

Drugs, medical progress,

Bipartisan Policy Center, Top Medical Innovation Priorities

National Institutes of Health

MAYO CLINIC CENTER FOR BIOMEDICAL DISCOVERY EXCEPTIONAL RESEARCH LEADS TO EXCEPTIONAL PATIENT CARE

NORDP Research Development Conference Research Development Strategy: Designing a De Novo Institute With Numerous Degrees of Freedom

1201 Maryland Avenue SW, Suite 900, Washington, DC ,

ehealth-strategien im Wettbewerb: Erfolgsfaktor oder schmückendes Beiwerk? ehealth Kongress Darmstadt, 17 Oktober 2014

Contents. Acknowledgments Preface What You ll Find in This Book How to Use This Book

A NATIONAL SURVEY OF EMERGENCY ROOM PHYSICIANS REGARDING THE FOOD AND DRUG ADMINISTRATION

PRO/CON: Is now the time for climate change laws in the U.S.?

The Importance of Participating in Clinical Trials in Alzheimer s Disease. Amanda G. Smith, M.D. Medical Director USF Health Byrd Alzheimer Institute

PhRMA Days Press Conference

Harvard Stem Cell Institute

LAUNCHING OF THE 2014 LAW 1715.

Improve your probability. of success

CANDIDATE INFORMATION PACK Head of Stand Up To Cancer

Moving to Implementation

Complex Adaptive Systems Forum: Transformative CAS Initiatives in Biomedicine

Governance of Nanotechnology and the Legislation in Preparation

Update on Current FDA Policies and Priorities

Moderna Therapeutics Announces Transition to a Clinical Stage Company, Provides Business Update and Outlines 2016 Strategic Priorities

The increase in overall life expectancy in the United States

HARVARD CFO OF THE FUTURE SUMMIT

Investing in Rare Disease Patient Advocacy Groups

Using patient-generated information to drive research and improve care. To drive research and improve care, we NEED patient-generated information

Id. 3. Id. Docket # USTR Edward Gresser Chair of the Trade Policy Staff Committee Office of the United States Trade Representative

Strategic Plan. Uniting to care & cure

CLINICAL TRIALS AND MARKET RESEARCH

FDA Driving Biomedical Product Innovation

Lead the way. Molecular Imaging. GE Healthcare. imagination at work

An Evidence-Based Approach to Hiring

Robert J. Beall, PhD, President and Chief Executive Officer Cystic Fibrosis Foundation

GUIDE HEA

medicines, improving the health of people around the world.

TESTIMONY ON AND. Mr. Chairman, Ranking Member Holt, and members of the Subcommittee:

IMI2: Strategic research agenda and overall approach Hugh Laverty Senior Scientific Project Manager

Access to Unapproved Drugs: Expanded Access and Right to Try

Prescription Drug Pricing Poll, conducted for Prescription Justice by Zogby Analytics *Margin of error +/- 3.1

HEARING TESTIMONY ARTHUR SANDS, M.D., PH.D. PRESIDENT AND CHIEF EXECUTIVE OFFICER, LEXICON PHARMACEUTICALS, INC. ON BEHALF OF THE

What is Precision Medicine?

FCDMF: PROJECT NEW HOPE 2017 STUDY ANNOUNCEMENT 7/3/2017

CTTI Overview One Decade of Impact. One Vision Ahead.

MONTEFIORE HEALTH SYSTEM

CRITICAL SUCCESS FACTORS

Aug. 28, 2017 Podcast Transcript

Innovative Tools States are using in Long Term Care and the Implication for HCBS

CHANGE MANAGEMENT. A Presentation by Ian Creery - January 30, The environment we re in How does change work?... 2

Hi, I'm Derek Baker, the Executive Editor of the ibm.com home. page, and I'm here today to talk with Dan Pelino, who Is IBM's General Manager for

Compassionate Use: The Ethics and Logistics of Using Investigational Medical Products outside of Clinical Trials

Operational Excellence in Healthcare. Creating a Culture of High Reliability: Driving Culture Change

Nodes and the Pharmaceutical Industry. Apps in Healthcare

Presidential Commission for the Study of Bioethical Issues 2 nd meeting September

The Role of the NIH Clinical Center in Translational and Clinical Research

OME 2013 summary of pitches

1201 Maryland Avenue SW, Suite 900, Washington, DC ,

CCTG initiative. patient reported outcomes (including wearables)

Robotic Process Automation. Robotic Process Automation Brings the Future to Your Workplace

THE IMPACT OF THE AFFORDABLE CARE ACT (ACA) ON CANCER RESEARCH, CARE, AND PREVENTION

TEN STEPS TO SYSTEM CHANGE Sustaining new ways of doing business takes a close look in the mirror.

Forging an agile, secure supply chain

Three steps to drive integrated care, faster. Start your transformation journey with the end in mind

Fielding high-performing innovation teams

It needs less of everything to create a given amount of value, so let s call it lean.

Statement on Drug Pricing in America: A Prescription for Change. Submitted to the Senate Finance Committee

Partnering for progress How collaborations are fueling biomedical advances

Annie Kennedy, Parent Project Muscular Dystrophy (PPMD) Testimony FDA PDUFA Stakeholder Meeting White Oak ~ December 17, 2015

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

Operational Excellence in Healthcare. Creating a Culture of High Reliability: Management System Fundamentals

Testimony of Molly Ventrelli Vice President, Regulatory Affairs Fresenius Kabi USA, LLC

SC&IS Corporate Information Sessions August 27, 2018 Atrium Business Building 6PM

NETWORKING AND CUREACCELERATOR LIVE!

Real World Evidence Generation in the 21 st Century: National Evaluation System for health Technology (NEST)

Transcription:

No longer just passengers, patients are now co-pilots helping to navigate the future of medical progress. But until recently, the pace of progress has been slow. In some diseases, we still utter the words "we haven't seen a new treatment in decades" with a straight face. Decades. Are we seriously accepting this? I recently heard a TedTalk by Andrew Solomon, "Depression, the secret we share," where he described the current treatment options for depression as being full of side effects, costly, and appalling all at the same time. But he is so grateful he lives now and not 50 years ago when there weren't treatment options. "I hope that 50 years hence people will hear about my treatments and be appalled that anyone endured such primitive science," Solomon said. Depression, cancer, Alzheimer's, Parkinson's disease, rare disorders - we could say this about so many areas. In fact, the list is long, and where there are treatments they almost always could be enhanced for patients. We've all heard the dismal statistics: 10,000 known diseases with only 500 treatments. Not great odds if you're a patient. And most

of us are, or will be at some point. At 15 years and over $1 billion to bring one new therapy from lab to market, we not only have work to do, we actually have an opportunity to do some of it - now. A perfect storm is brewing - and patient engagement is at its epicenter. It's a long, storied history to get us to this point. From the March of Dimes to the Patient's Bill of Rights to the ACT UP movement, patient-driven efforts pushed boundaries that allowed the medical research and healthcare systems to pave new ground. We are at a turning point once again with the 21st Century Cures Act (H.R. 6). Passed unanimously by the House Committee on Energy and Commerce, it sets out to cut through the complexity, bureaucracy, and inefficiency in our over-100-year-old national research infrastructure, and puts in place the resources and tools necessary for our system to catch up to the cutting-edge science happening every day in labs across the country. Most importantly, it gives patients an actual voice and vote in this transformation by proposing the inclusion of patient representatives in nearly every council, panel, advisory board, and body that would be created under the act. This is it - our time, the next big chapter of patient engagement and advancing treatments and cures. We can't afford to delay and squabble while patients who need cures lie in wait. This legislation is borne from the spirit of compromise and the tenacity and vision of Chairman Fred Upton, Congresswoman Diana DeGette, and countless others who see this as a chance for our United States Congress to do some of the people's business. It's the right time for 21st Century Cures for so many reasons: 1) Seizing the moment - science is ripe Our scientific progress is moving forward at a faster and faster pace, and we already have both the understanding of human biology and the advanced technology necessary to tackle questions that previously vexed researchers and drug developers.

The genome has been mapped, many people have electronic medical records, and data about our bodies and diseases are being collected in mass quantities everywhere from doctor's offices to patient registries to our own smartphones. If we don't act now, we risk losing the ability to not only capitalize on our tremendous scientific knowledge, but also to maintain our global leadership in bioscience. "Complex diseases require complex solutions. Patients can now anticipate earlier access to those lifesaving solutions because 21st Century Cures legislation expands resources, incentivizes creativity, accelerates regulation, and, most importantly, facilitates data sharing across the discovery, development, and delivery of innovative drugs and medical devices." -- Andrew von Eschenbach, former Director, National Cancer Institute; former Commissioner, U.S. Food and Drug Administration; Senior Fellow, Milken Institute 2) Investing in our priorities The 21st Century Cures act, also known as "Cures2015," includes critical, sustained funding for the National Institutes of Health ($10 billion over five years) and the U.S. Food and Drug Administration ($550 million over five years) that can be deployed as early as FY 2016. That means funding for the best and brightest young researchers, support for risky but promising science, and the capacity-building necessary to pull our national institutions into the 21st century. "The increased NIH funding proposed in Cures2015 is heroic. Cures2015 would restore the medical research funding that has been lost to inflation and spending cuts over the past decade. Representatives Upton, Pallone, and DeGette have worked together in a bipartisan way to show that Congress can act for millions of American patients and their families. Act for patients, act for NIH, support Cures2015." -- Pat White, President, ActforNIH

3) Making collaboration HAPPEN The notion of working together toward aligned goals rings true in the war against a daunting and unyielding enemy: disease. And yet, making collaboration happen every single day does not come naturally in a system built with incentives that undermine teamwork. H.R. 6 cuts through roadblocks to sharing and analyzing the massive amounts of health data generated in research and clinical settings, which is currently locked away in silos across the medical research ecosystem. "This is a mind-exploding problem, but it's one that we can solve. We've proven over the last decade that scientists know how to work together, and they want to work together, and I think we have to enable that." -- Anna Barker, Director, Transformative Healthcare Networks, Co-Director, Complex Adaptive Systems Initiative and Professor, School of Life Sciences, Arizona State University; Senior Fellow, FasterCures 4) Advancing the science of patient input What if we actually worked with the patients whose conditions we are trying to improve? What if we learned from the past decades of patient engagement, from the creation of the March of Dimes to HIV/AIDS activism to the launch of patient-focused drug development? What if this was our next big chapter? "Never before in this country have we had so much scientific potential being impeded by lack of biomedical research funding, inefficient or poorly designed clinical trials, and research and development practices that fail to put the needs of patients front and center. The greatest frustration for me is knowing what we could be doing for patients in this country that we don't do, and not because we don't have the scientific knowledge or technology, but because of bureaucracy, culture, or antiquated practices. The bipartisan commitment to 21st Century Cures sets the course to get cures to patients faster and put our nation back on the map as a global leader in science and innovation." -- Bray Patrick-Lake, Director of Stakeholder Engagement, Clinical Trials Transformation Initiative; Co-Chair, Advisory

Committee to the NIH Director on the Precision Medicine Initiative "This legislation makes a bold investment in critical science and research, and builds a framework to better involve and incorporate patients as the top priority throughout the process." -- Ellen Sigal, Chair and Founder, Friends of Cancer Research This is an historic moment - with the whole of the R&D ecosystem and the federal government coming together across sectors, diseases, and political parties to fix the system for patients, and improve all of our odds. Who knows when (or if!) we'll have this opportunity again. Disease doesn't wait, and neither can we. Follow Twitter Author Follow Margaret Anderson on Twitter: www.twitter.com/margaretaindc Follow Tag Links Bottom MORE: 21st Century Cures Nih Fda Medical Research Patients Cures Fastercures HIV/AIDS March of Dimes Fred Upton Diana DeGette House Energy & Commerce Committee