Regulatory Market Update: What are the major changes and differences worldwide?

Similar documents
Orphan Products and Drug Development 2015 MARLENE E. HAFFNER, MD MPH HAFFNER ASSOCIATES AS PRESENTED TO GLG SEPTEMBER 23RD, 2015

Clinical Trial Methods Course 2017 Trials in Rare Diseases. Erika Augustine, MD, MS University of Rochester Medical Center August 10, 2017

The Construction of a Clinical Trial. Lee Ann Lawson MS ARNP CCRC

Industry Perspective: The Challenges and Benefits in using Expedited Regulatory Pathways

Copyright. Jeremiah J. Kelly (2015). All rights reserved. Further dissemination without express written consent strictly prohibited.

AN INSIGHT ON ORPHAN DRUG DEVELOPMENT STRATEGY IN US AND EUROPE

Agenda: Opportunities in Developing Orphan Drug Products. Mukesh Kumar, PhD, RAC

Sec Short title; finding. Sec Authority to assess and use drug fees. Sec Reauthorization; reporting requirements.

GREAT STRIDES IN SCIENCE WHAT ABOUT ACCESS? Marlene E. Haffner, MD, MPH 2nd IRDiRC Conference Shenzhen, China November 8, 2014

Dr. Sanders is a consultant to Accordant Health Services and Jacobus Pharmaceutical Co.

OBSTACLES TO TRANSLATION

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

Rare Diseases and CDER: Challenges and Opportunities

February 15, Re: Docket No. FDA-2017-D-6159: Expedited Programs for Regenerative Medicine Therapies for Serious Conditions

Orphan Drug Designation within the Development Strategy

Center for Drug Evaluation and Research. CDER Small Business and Industry Assistance. (CDER SBIA) and New Drug Review.

While individually rare, orphan diseases are actually collectively common, with an OF ORPHAN DRUG DEVELOPMENT MEETING THE UNIQUE CHALLENGES

Yes, You Can Teach an Old Drug New Tricks: Regulatory Pathway for Repurposed Drugs

Fast track Approval process- Ethical considerations

Topics Covered. FDA s Role in Expediting the Development of Novel Medical Products. How a Regulatory Agency Comes into Existence 3/5/2018

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

New Drug Application (NDA) Webinar December 6, 2016

Rare Diseases: Challenges and Opportunities NIH Perspective

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

The Evolving Regulatory Landscape for Orphan Drugs: FDA Perspectives

Docket #: FDA-2018-D-3268

Insights into Rare Disease Drug Approval: Trends and Recent Developments

FDA from a Former FDAer: Secrets and insights into regulatory review and drug development

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

Clarification of Orphan Designation of Drugs and Biologics for Pediatric Subpopulations of Common Diseases

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

Pediatric Cancer Drug Development: Impact of US Regulations

Speed your time to market with FDA s expedited programs

Structure and Mandate of FDA

The 21st Century Cures Act

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

US Regulatory Tools for Expedited Antibacterial Development Programs

Office for Human Subject Protection. University of Rochester

Considerations for Global Development of Orphan Drugs. Ginny Beakes-Read Executive Director Global Regulatory Policy and Intelligence Eisai, Inc.

The Intersection of Genomics Research and the IDE Regulation

Antisense Therapeutics Ltd ASX:ANP January 2017

Health Industry Alert

Accelerated Approvals

FDA EMA/FDA/MHLW-PMDA

Re: Docket No. FDA-2018-D-1895: Indications and Usage Section of Labeling for Human Prescription Drug and Biological Products Content and Format

Johan Christenson MD; PhD Partner Farmasidagene 2014 Oslo

EUROPEAN COMMISSION DIRECTORATE-GENERAL FOR HEALTH AND FOOD SAFETY

Insights into the Rare Disease Drug Approval Landscape: Trends and Current Development

The Need for, and Application of, Natural History Data in Orphan Disease Medical Product Development

2015 Policy Landscape: A Biomedical R&D Planning Guide

Medical Device Regulations

Rare Diseases Drug Development and Patient Perspective Initiatives at FDA

Re: Docket No. FDA-2014-D-1461: Rare Pediatric Disease Priority Review Vouchers

Type of Activity. Universal Activity Number L04-P

Modernizing the Food and Drugs Act to Accommodate a Product Lifecycle Approach

US FDA Expedited Programs and Expanded Access

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

EXPANDED ACCESS: RECENT LEGISLATION AND POLICY UPDATE

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

D. Enhancing Regulatory Science and Expediting Drug Development:

Drug Development & the FDA Pharmacy 309 November 2005

Chin Koerner Executive Director US Regulatory and Development Policy

LJ October 2011 COMM-1 Intro to Speech Favorable Legislation for the Production of Orphan Drugs

COMMITTEE FOR MEDICINAL PRODUCTS FOR HUMAN USE (CHMP)

Solving the Problem of New Uses

VIVEK VIKRAM SINGH, SUBJECT MATTER EXPERT, RESEARCH & ANALYTICS CAN COMPETITIVE INTELLIGENCE STRATEGIES HELP IN ORPHAN DRUG DEVELOPMENT?

Initial Draft Discussion Document for A Canadian Orphan Drug Regulatory Framework

General Comments. May 30, Division of Dockets Management (HFA-305) Food and Drug Administration 5630 Fishers Lane, Room 1061 Rockville, MD 20852

Pharmamarketing - strategic challenges

Stem Cell Research: Identifying emerging high priority policy issues

May 13, Washington, DC Washington, DC Washington, DC Washington, DC 20515

Expanded Access and the Individual Patient IND

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

Acquisition of Vtesse Inc. Increased Focus on Orphan and Pediatric Diseases

Streamlining IRB Procedures for Expanded Access

IDSA is pleased to offer the following comments on specific priority areas identified by FDA:

The Children s Hospital of Philadelphia Committees for the Protection of Human Subjects Policies and Procedures Determination of IND/IDE Requirement

Facilitating Antibacterial Drug Development Outlining the Path Forward

Patient Protection and Affordable Care Act (H.R. 3590) Approval Pathway for Biosimilar Biological Products

Regulatory update from Europe:

Regulation of Microbiota- Based Products

Disclosures. Laboratory Stakeholders. IVD vs. LDT. FDA Regulation of Laboratory Developed Tests 10/2/2015. FDA Regulation of LDTs

Scientific advice and its impact on marketing authorisation application reviews

IRB APPLICATION OF FDA REGULATIONS Click for Animation

Bipartisan Policy Center, Top Medical Innovation Priorities

The Big Picture of FTD Research: Funding, Collaboration and the Scoop on Participation

Regulatory frameworks of regenerative medicines and products review in Japan

Alliance for Regenerative Medicine

Patient Focused Drug Development 2.0

INSTITUTIONAL RESEARCH Healthcare and Technology INDUSTRY NOTE Member FINRA/SIPC

Volunteering for Clinical Trials

May 19, Dear Members of the United States House of Representatives:

Availability of Masked and De-identified Non-Summary Safety and Efficacy Data; Request for

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

Pediatric Exclusivity and Drug Development Requirements in the Overall Pediatric Population. Prepared by Beckloff Associates, Inc.

The Emerging Role of Post-Market Evidence Generation in Decision-Making: Linkages to the Product Lifecycle Approach

ARIKAYCE U.S. FDA Approval

Regulatory Updates in Taiwan

BREAKTHROUGH INNOVATION: LESSONS FOR PHARMA R&D

Health Industry Alert

Transcription:

Regulatory Market Update: What are the major changes and differences worldwide? Marlene E. Haffner MD, MPH, CEO Haffner Associates Orphan Drug Summit 2015 Copenhagen, Denmark September 17, 2015

Orphan Drug Landscape Orphan Drugs are IN Estimated worth of the global market - $50 Billion Percentage of orphan drugs with annual sales > 1 billion $ - 29% Percentage of orphan drugs with additional rare disease indications 15% 460+ Orphan products under FDA review in U.S. (2014) A record 291 orphan drug designations were granted in the US in 2014 49 Orphan Products approved 2014 Same standards for review and approval as non-orphans except for FDA flexibility - Sources: NORD, Orphanet, Evaluate Pharma, PhRMA, Thomson Reuters, FDA

Where In The World Is Orphan Drug Policy

Orphan Drugs in US Orphan Drug Act (1983) Rare disease = prevalence < 200,000 7 Year Market Exclusivity FDA Filing Fee Wavier Tax Credits for clinical trials Orphan Product Grants ~494 drugs approved; >3400 designated (FDA) Use of accelerated approval/fast track/pediatric voucher/breakthrough designation

Common EMEA/FDA Application for Orphan Medicinal Product Designation Sponsor may apply for orphan designation of the same medicinal product for the same use in both jurisdictions by using this common application Still independent review from each agency FDA no longer requires a statement of party of interest for an orphan drug designation

Regulatory Changes FDA investigational new drug application is filed with the FDA for drugs that appear safe in the preclinical phase Drug vs. placebo Phase 0 including therapeutic or diagnostic intent Biologics Price Competition and Innovation Act of 2009 (BPCI Act) EMEA Assessment is conducted by national agencies of member states Enforcement is done by member states with help of EMEA application for a marketing authorization license is filed with the EMEA Drug vs existing drug Improving coordination Microdose trials

Regulatory Changes in Drug Approval Accelerated Process Serious conditions that filled an unmet medical are permitted to be approved based on a surrogate endpoint Priority Review 6 month response from FDA 21 st Century Act - emphasis on medical devices Fast Track Facilitates development and expedites review for drugs that treat serious conditions and fill unmet medical need Breakthrough Expedite development and review of drugs that demonstrate substantial improvement over available therapy Pediatric Voucher Extends priority review for new drugs that are developed to treat rare pediatric diseases Can be used in combination with other incentive programs Increased emphasis on safety post approval monitoring

Approval Timeline

Challenges in developing drugs across borders Cultural differences Prescribing practices Trade agreements / parallel trade offers - IP Price Controls who is paying? Direct-to-consumer (DTC) advertising Differences in regulation

21 st Century Cures Act - US Increases funding for NIH and FDA Data Access expand surveillance of neurological diseases revise health information privacy rules implement a system that allows further research on clinical trial data Orphan Product Extensions Now; Incentives for Certain Products for Limited Populations Section 2151 - FFDCA is amended to extend market exclusivity by six months Section 2152 - priority review voucher program Extended for pediatric diseases through 2018 apply only to serious diseases Streamlining Clinical Trials No consent required for medical devices that pose minimal risk IRB reviews for clinical testing of medical devices no longer needs to be local

Open Act HR971- US Proposed legislation from the senate Extends market exclusivity by 6 months for repurposed drugs that are approved to prevent, treat, or diagnose a new indication of rare disease Requires indication from FDA on label Requires FDA to inform the public of products that receive extension Limits the product for one extension Applies only to new indications after the Act is passed Extension can be revoked only through untrue statements on application

Questions? Marlene E. Haffner, MD, MPH President & CEO 11616 Danville Drive Rockville, Maryland 20852 mhaffner3@verizon.net 301 984 5729 - office 301 641 4268 - cell 301 984 2272 - FAX