Pfizer Program in DMD. Beth Belluscio, MD-Ph.D. Pfizer Rare Disease September 9, 2017

Similar documents
DUCHENNE MUSCULAR DYSTROPHY CLINICAL DEVELOPMENT PROGRAM

Catabasis Pharmaceuticals Reports First Quarter 2018 Financial Results and Reviews Business Progress

Antibody against Chikungunya virus (mrna-1944)

-- Study achieved statistical significance on all primary and secondary biological endpoints --

Gene therapies for SMA and DMD

SMTC1100: Progressing to Patient Clinical Trials

A roadmap for bringing FKRP gene therapies into clinical use

NS-065/NCNP-01 Phase 2 dose finding study

Prosensa s continued development of exon-51 skipping with drisapersen after the failure of its phase-iii clinical trial.

Exon Skipping. Wendy Erler Patient Advocacy Wave Life Sciences

Prosensa Therapeutics R&D in ultra-rare disease

ARTICLE DISCUSSION: MARCH 2018 IRB MEMBER TRAINING

CAP-1002: HOPE Clinical Trials PPMD Annual Conference 2018

Innovative treatments in neuromuscular disorders

Regulatory Perspectives on Gene Therapies for Rare Diseases Rare Diseases Forum Washington, D.C. October 17, 2018

Medical Policy An independent licensee of the Blue Cross Blue Shield Association

Together, all nine participants have reduced infusions of factor IX concentrates by 99 percent over cumulative 1,650 days

-- Sarepta strengthens position as a leader in gene therapy; expands rare disease franchise --

Prosensa announces commencement of redosing of drisapersen in North America in patients with Duchenne muscular dystrophy

Drug Development and Clinical Trials Pat Furlong Parent Project Muscular Dystrophy

PTC Therapeutics: 20 years of commitment to bringing new treatments to patients with rare disorders. March 2018

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

Muscle-specific CRISPR/Cas9 dystrophin gene editing

Duchenne Muscular Dystrophy

ataluren overview A New Approach to Genetic Disorders

CRISPR/Cas9 and genome editing for genetic neuromuscular disorders

PTC Therapeutics: 20 years of commitment to bringing new treatments to patients with rare disorders JANUARY 2018

Recombinant Biglycan for the Treatment! of Duchenne Muscular Dystrophy!!! PPMD Annual Conference, Jun 2013! By Joel B. Braunstein, MD!

Advancing Mitochondrial Medicine. Günther Metz, SVP Business Development

This presentation contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform

About Sarepta Therapeutics

Swissmedic Accepts Santhera's Filing of SNT-MC17 in Friedreich's Ataxia

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

Delivering on the Promise of RNA- Based Therapeu;cs

Advancing Manufacturing for Advanced Therapies

Accelerating Cures: Addressing Unmet Patient Need Or Putting Patients At Risk? Speaker

Mustang Bio Reports Third Quarter 2018 Financial Results and Recent Corporate Highlights

Sarepta Therapeutics, Inc. (SRPT-NASDAQ)

Corporate Presentation OCTOBER 2018

Rimeporide in Duchenne Muscular Dystrophy January Photo credits : Ceridwen Hughes,

TRANSLATIONAL RESEARCH IN RARE AND NEUROMUSCULAR DISEASES - WHY DATA SHARING MATTERS. H a n n s Lochmüller, Newcastle University

Phase 1 SMA Type 2 Trial Initiation and Study Design. December 2017

Pfizer Completes Acquisition of Hospira

FRDA CLINICAL TRIALS. Susan L. Perlman, M.D. Clinical Professor of Neurology UCLA Medical Center. Meeting

TITLE: Translational Studies of GALGT2 Gene Therapy for Duchenne Muscular Dystrophy

uniqure Announces First Clinical Data From Second Dose Cohort of AMT-060 in Ongoing Phase I/II trial in Patients with Severe Hemophilia B

Chimerix Announces First Quarter 2017 Financial Results

Regulatory Innovations in Neurological Disorder Therapies, including Spinraza and Exondys 51

Corporate Presentation. January 7, 2019

Results to be Presented at LDN WORLD Symposium in February Initiation of Repeat-Dose Pompe Study Anticipated in 3Q13

PATHWAY TO VALUE CREATION NASDAQ: BNTC ASX: BLT

PATHWAY TO VALUE CREATION NASDAQ: BNTC ASX: BLT. For personal use only

Gene therapy. Findings by Alert

DMD Research Overview End Duchenne Tour Susan T. Iannaccone, MD Associate Director UTSW Wellstone MDC

Dr. Leslie Hudson President and CEO AVI BioPharma

NASDAQ: ABEO

Fourth Quarter and Full Year Financial and Operational Results Conference Call March 21, 2018

Stealth BioTherapeutics Mission:

ROLE OF ADVOCACY IN FACILITATING BASIC SCIENTIFIC RESEARCH Purpose of Advocacy Help Solve Important Problems

Corporate Presentation. March 2018

Second Quarter 2017 Financial Results. August 8, 2017

Gene Therapy for Hemophilia A: Are we really getting better?

+61 (0)

FDA Regulation of Companion Diagnostics

GENENTECH PROVIDES UPDATE ON PIPELINE AGENTS AT THE AMERICAN SOCIETY OF CLINICAL ONCOLOGY MEETING

Consortia-Based Strategies in Neurodegenerative Diseases: Critical Path Institute s Track Record in Collaborative Efforts

Supplementary Appendix

This presentation contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform

Gene Therapy: The Basics. Mark A. Kay MD PhD Dennis Farrey Family Professor Stanford University

Course Agenda. Day One

Planned Acquisition of Nightstar Therapeutics

CATALYST BIOSCIENCES. Corporate Overview. 9 April 2019

CENTER DIRECTOR DECISIONAL MEMO

Conference call transcript for the March 2017 Quarterly Report

Advancing New Treatments for DMD and C. difficile Infection

Dear Dr. Janet Woodcock and colleagues at the FDA,

UNDERSTANDING GENE REPLACEMENT THERAPY

Total urinary GAGs declined by 51%, dermatan sulfate by 32%, and heparan sulfate by 61% in Cohort 2 at 16 weeks

The (im)perfect Advocacy Organization Pat Furlong

Patient Focused Drug Development 2.0

The Leader in AAV Gene Therapy. A Guide to AAV Gene Therapy for MPS I and II

Jefferies Healthcare Conference. June 2016

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

Drug development and evaluation with small clinical Trials from the regulatory point of view

Agios Pharmaceuticals, Inc.

Stifel Nicolaus Healthcare Conference. September 2012

Q4 and Full Year 2017 Conference Call. February 22, 2018

vision is our mission NASDAQ: OPHT October 2018

The Road to Treatment 2

Unlocking protein production with translational read-through for rare genetic diseases

HD Regulatory Science Consortium (HD-RSC) A consortium aimed at accelerating treatments for Huntington s disease

Corporate Presentation JANUARY 2019

European Medicines Agency decision

Torreya acted as exclusive financial advisor to Lysogene. About MPS IIIA and LYS-SAF302

-- Expands Sarepta s portfolio to as many as 14 gene therapy programs --

Second Quarter 2017 Earnings Teleconference. August 1, 2017

Duchenne Muscular Dystrophy and Related Dystrophinopathies: Developing Drugs for Treatment Guidance for Industry

Clinical Trial Paradigms in CNS Gene Therapy. Bernard Ravina, MD, MS Chief Medical Officer, Praxis Precision Medicines October 16, 2018

Karyopharm Reports Second Quarter 2016 Financial Results and Highlights Recent Progress

Investor Presentation. October 2018

Transcription:

Pfizer Program in DMD Beth Belluscio, MD-Ph.D. Pfizer Rare Disease September 9, 2017

Myostatin Inhibitor for the Potential Treatment of Duchenne Muscular Dystrophy

Disclaimer This presentation includes forward-looking statements about, among other things, development of Pfizer s Rare Disease products and product candidates, including domagrozumab, including their potential benefits, that are subject to substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Additional information regarding these factors can be found in Pfizer s Annual Report on Form 10-K for the fiscal year ended December 31, 2016 and in our subsequent reports on Form 10-Q, including in the sections thereof captioned Risk Factors and Forward-Looking Information and Factors that May Affect Future Results, as well as in our subsequent reports on Form 8-K, all of which are filed with the US Securities and Exchange Commission (SEC) and available at www.sec.gov and www.pfizer.com. The forward-looking statements in this presentation speak only as of the original date of this presentation, and we undertake no obligation to update or revise any of these statements Property of Pfizer Inc., Not for distribution 2

Domagrozumab (PF-06252616): Phase II Development in Duchenne Muscular Dystrophy (#NCT02310763) Period 1 (48W) Period 2 (48W) Sequence 1 Low dose Medium dose High dose High dose High dose High dose Sequence 2 Low dose Medium dose High dose Placebo Placebo Placebo Sequence 3 Placebo Placebo Placebo Low dose Medium dose High dose 6-<16 year old boys with DMD Ambulant on steroid Monthly 2hr IV infusion Dose escalation N=35 Randomized per sequence (Total 105) Enrollment completed Primary Analysis 4 Stair Climb time NSTAR, 6MWT, Strength MRI and DXA imaging Safety biomarkers External Data Monitoring Committee Secondary Analysis 3

Gene Therapy for the Potential Treatment of Duchenne Muscular Dystrophy 1

What is Gene Therapy? Therapeutic Gene Therapeutic Protein Modified viral particle Vector Muscular Dystrophy Association Intravenous injection of vectors Therapeutic Gene Muscular Dystrophy Association 1. Certain viral genes are replaced with therapeutic genes to produce a vector. 2. Vectors are injected into the bloodstream where they find their way to specific tissues or organs. 3. The vector delivers the therapeutic gene to a cell where it is used as a blueprint to make the missing protein. 6 Property of Pfizer Inc., Not for distribution

Towards a Gene Therapy for Duchenne Muscular Dystrophy Mini-dystrophin delivered by gene therapy is produced throughout the skeletal muscles and hearts of rats and dogs who lack dystrophin Mini-dystrophin expressed for up to 8 years in dog that lacks dystrophin Functional improvements seen in animal models Preclinical studies to select a dose for a human trial are complete Jelly at age 8 still produced minidystrophin in her muscles Orphan Drug status achieved in US and Europe Rare Pediatric Disease designation received from FDA Phase I/II human trial planned within the next 12 months (Based on the pioneering work of Dr. Samulski and Dr. Xiao) 7 Property of Pfizer Inc., Not for distribution

Gene Therapy for Duchenne: The Knowns and Unknowns Knowns: Unknowns: Gene therapy cannot be undone once administered Gene therapy eligibility is not determined by having a particular mutation Not everyone will be eligible: Those with pre-existing antibodies to the virus AAV9 will not be eligible, at least initially Will the effect be permanent? Can gene therapy be readministered? Will clinical trials for other types of drugs exclude boys who have previously participated in a gene therapy study? Will the problem of pre-existing antibodies be overcome to make gene therapy an option for more people? 8 Property of Pfizer Inc., Not for distribution