We are committed to translating ground-breaking science into genomic therapies that transform patients lives

Similar documents
Russell DeKelver, PhD Sangamo BioSciences, Inc.

Sangamo Therapeutics Announces Presentations at 2017 Annual meeting of the American Society of Gene & Cell Therapy

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

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

Non-viral Delivery of ZFN mrna Enables Highly Efficient In Vivo Genome Editing of Multiple Therapeutic Gene Targets

Jefferies 2017 Global Healthcare Conference. Dr Sandy Macrae CEO June 9, 2017

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

Corporate Presentation. March 2018

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

SANGAMO THERAPEUTICS, INC. (Exact name of registrant as specified in its charter)

Corporate Presentation JANUARY 2019

Jefferies 2016 Healthcare Conference Engineering Genetic Cures

5/27/2014. William D. Chip Baird, Chief Financial Officer

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

Sumiti Jain. [Poster #2003, Tuesday February 13 th ] February 12 th, 2018

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

Gene Editing and Targeted Integration Using Zinc Finger Nucleases for Subjects with Mucopolysaccharidosis I (MPS I)

Sangamo BioSciences Reports Third Quarter 2014 Financial Results

Designed Zinc Finger Protein Transcription Factors for Single-Gene Regulation Throughout the Central Nervous System

Protalix BioTherapeutics Corporate Update. June 2016

Protalix Corporate Presentation June 2015

Welcome to the Webinar! Human Genome Editing: Latest Developments and Advancements

HYDRODYNAMIC GENE TRANSFER OF ALPHA-GALACTOSIDASE (GLA) IN THE GLA KNOCKOUT MOUSE PARTIALLY REVERSES BIOCHEMICAL DEFICITS.

TIDES 2014 GalNAc-siRNA with Enhanced Stabilization Chemistry: ESC-GalNAc-siRNA. May 14, 2014 Muthiah Manoharan

NASDAQ: ABEO

Building on our specialty expertise. Shire acquires Transkaryotic Therapies Inc.

Grants Awarded in 2006

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

Gaucher Clinic 2007: Clinical trials

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

Immuno-Oncology Program

Jefferies 2014 Global Healthcare Conference

Pre-Clinical Evaluation of ALN-AAT to Ameliorate Liver Disease Associated with Alpha-1 Antitrypsin Deficiency

Human alpha-galactosidase A / GLA ELISA Pair Set

CNS Gene Regulation Platform

John F. Crowley, Chairman & CEO

This presentation contains forward looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 relating to business,

Hemophilia and Gene Therapy

Preclinical development for SSc indications NO COPY. a preclinical portfolio in a perfect world. Jörg Distler

SANGAMO THERAPEUTICS, INC. (Exact name of registrant as specified in its charter)

Understanding Gene Therapy. April 26, 2016

Wedbush PacGrow Healthcare Conference August 15, 2018

Investigating Critical Challenges in the Gene Therapy Field

Session 1: Disease clustering to guide trial design and analysis

10/07/2018. Liver directed gene therapy. - An overview. DNA/RNA therapies for Wilson s disease. The liver, organ of choice. Highly vascularised

Genome editing. Knock-ins

Corporate Presentation OCTOBER 2018

VELTIS : INNOVATIVE ALBUMIN BASED TECHNOLOGY FOR HALF- LIFE EXTENSION AND OPTIMIZATION OF BIOTHERAPEUTICS

Developing Targeted Stem Cell Therapeutics for Cancer. Shawn Hingtgen, Ph.D. Assistant Professor UNC Eshelman School of Pharmacy May 22 nd, 2013

Mutagenesis and Expression of Mammalian Clotting Factor IX. Mark McCleland The Children s Hospital of Philadelphia and Lycoming College

Discovery of drugs and drug resistance. Model organisms. Plants and livestock. Cell-based disease modelling. Therapeutics

Bart Williams, PhD Van Andel Research Center

Protalix BioTherapeutics Corporate Update. June 2017

Spark Therapeutics, Inc.

A roadmap for bringing FKRP gene therapies into clinical use

Sangamo BioSciences Reports First Quarter 2014 Financial Results

Cell and Gene Therapy Catapult clinical trials database

Disclosure. Hemophilia: The Royal Treatment. Objectives. Background. History of Hemophilia. Epidemiology 1/4/2018

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

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

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

How Targets Are Chosen. Chris Wayman 12 th April 2012

Sangamo BioSciences Reports Third Quarter 2013 Financial Results

Curing rare disease in a single dose. Just as enzyme replacement therapies (ERTs) revolutionized the past, gene therapy has the potential to

Expectations for Biodistribution (BD) Assessments for Gene Therapy (GT) Products

Use of Antisense Oligonucleotides for the Treatment of Inheritable Rare Disorders. C. Frank Bennett Isis Pharmaceuticals

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

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

Protalix BioTherapeutics Corporate Update. January 2017

HUMAN GENOME EDITING FAQs

Predicting Tissue Distribution & Clearance of Antibody Formats to Improve Selectivity of Targeted Therapies

35 th Annual J.P. Morgan Healthcare Conference. John F. Crowley, Chairman and Chief Executive Officer January 10, 2017

Fig. 5.1(a) and Fig. 5.1(b), on page 3 of the insert, show some changes that take place in the fermenter over the first 6 days.

Pre-existing anti-viral vector antibodies in gene therapy

International Consortium For Innovation & Quality in Pharmaceutical Development

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

BioCentury Future Leaders Conference. March 20, 2015

Gene Therapy: Fellow s Conference Fred Hutchinson Cancer Research Center. Zandra K. Klippel

37 th Annual J.P. Morgan Healthcare Conference

Gene Therapy Studies

History of RNAi Therapeutic Delivery at Arrowhead Pharmaceuticals

The Road to Treatment 2

Corporate Overview. January Investor communication only: Not for use in promotion

Course Agenda. Day One

Update from the Center for Biologics Evaluation and Research (CBER) Peter Marks, M.D., Ph.D. GMP By The Sea 2017

Medical Topics: Gene Therapy. E. Anne Jackson, FSA MAAA July 30, 2018

Plant Made Biopharmaceuticals NEXT-GENERATION THERAPEUTICS FOR ORPHAN DISEASES

Credit Suisse 27th Annual Healthcare Conference. John F. Crowley, Chairman and Chief Executive Officer November 14, 2018

Genome editing: clinical applications FYODOR URNOV

Opportunities for Accelerating Cell Line Development and Beyond

Supplementary Figures and Figure legends

Stem cells in Development

6th Form Open Day 15th July 2015

CRN 18-mo progress update

Why do we care about homologous recombination?

UNDERSTANDING GENE REPLACEMENT THERAPY FOR GENETIC DISEASES

Corporate Overview. September 2016

pegunigalsidase alfa Prague November 24, 2017 Raphael Schiffmann, M.D., M.H.Sc. Preclinical and clinical

Cell-penetrating peptides: news for dated cellular Trojan horses

SDR and SRG SCID Rats

Transcription:

We are committed to translating ground-breaking science into genomic therapies that transform patients lives Liver-based expression of the human alpha-galactosidase A gene (GLA) in a murine Fabry model results in continuous high levels of enzyme activity and effective substrate reduction Preclinical data supporting a gene therapy for Fabry Disease Thomas Wechsler, Ph.D May 10 th, 2017

In 2017, Sangamo is focused on enrolling four clinical trials including the first ever human in vivo genome editing studies Four lead clinical development programs Research Preclinical Phase 1/2 Phase 3 Hemophilia A Hemophilia B MPS I MPS II Phase 1/2 Phase 1/2 Phase 1/2 Phase 1/2 In Vivo Gene Therapy In Vivo Genome Editing 2

Fabry Disease is a lysosomal storage disorder Fabry disease is an X-linked monogenic disease caused by mutations in GLA gene encoding the enzyme alpha-galactosidase A (α-gal A) α-gal A plays a role in degradation of globotriaosylceramide (Gb3) and Lyso-Gb3 The liver is a significant source of Gb3/Lyso-Gb3 storage material accumulating in lysosomes of endothelial cells, kidney and heart Depending on residual enzyme activity there are two major phenotypes: Type I - Classic Fabry: <1% of α-gal A activity; 1 : 40,000 Type II - Later-onset Fabry: >1% of α-gal A activity; ~ 1 : 5,000 Desnick lab Lysosomal Gb3 inclusion (kidney) 3

Fabry Disease is a progressive systemic disease Skin: Angiokeratoma Hypohidrosis Heart: Early dysfunction to cardiac death Nervous System: Neuropathy Stroke (~7%) Standard of care is enzyme replacement therapy (ERT): Recombinant a-gal A is produced in CHO cells Biweekly infusion (2-4 hr) of a-gal A Annual cost: ~ $ 250,000 per patient Unmeet needs: Cardiac Gb3 clearance Podocyte Gb3 clearance Neuropathic pain Long-term stroke risk Other therapeutic strategies: Kidney: Progressive renal dysfunction leading to failure and dialysis Early symptom Late symptom 4 HSC gene therapy Pharmacological chaperone therapy Substrate reduction therapy

Fabry Disease is a progressive systemic disease Skin: Angiokeratoma Hypohidrosis Heart: Early dysfunction to cardiac death Kidney: Progressive renal dysfunction leading to failure and dialysis Early symptom Late symptom Nervous System: Neuropathy Stroke (~7%) ERT Standard of care is enzyme replacement therapy (ERT): Recombinant a-gal A is produced in CHO cells Biweekly infusion (2-4 hr) of a-gal A Annual cost: ~ $ 250,000 per patient Unmeet needs: Cardiac Gb3 clearance Podocyte Gb3 clearance Neuropathic pain Long-term stroke risk Other therapeutic strategies: HSC gene therapy Pharmacological chaperone therapy Substrate reduction therapy

Fabry Disease is a progressive systemic disease Skin: Neuropathy Heart: Early dysfunction to cardiac death CNS: Stroke (~7%) Standard of care is enzyme replacement therapy (ERT): Recombinant a-gal A is produced in CHO cells Biweekly infusion (2-4 hr) of a-gal A Annual cost: ~ $ 250,000 per patient Unmeet needs: Cardiac Gb3 clearance Podocyte Gb3 clearance Neuropathic pain Long-term stroke risk Other therapeutic strategies: Kidney: Progressive renal dysfunction leading to failure and dialysis Late symptom HSC gene therapy Pharmacological chaperone therapy Substrate reduction therapy 6

Advantages of liver-directed gene therapy Liver-based AAV gene therapy has the following potential advantages: AAV Convenience Single administration versus biweekly infusions Efficacy Constant supply of therapeutic enzyme (versus peak/trough) may lead to better efficacy in target tissues compared to ERT Tolerance Liver expression may lead to tolerization towards transgene

cdna gene therapy Two approaches of single administration treatments for Fabry Disease In vivo genome editing AAV vector Therapeutic gene AAV AAV vectors Zinc Finger Nuclease (ZFN) 1 and 2 Therapeutic gene Liver Cell Nucleus Strong albumin Promoter Promoter Albumin locus Therapeutic Gene Therapeutic gene Liver Cell DNA Episomal therapeutic transgene with liver specific promoter Liver produces and secretes therapeutic enzyme with glycosylation suitable for tissue uptake and lysosomal delivery H TG H Homology arm Integrated therapeutic transgene using albumin promoter 8

cdna gene therapy Two approaches of single administration treatments for Fabry Disease In vivo genome editing AAV vector Therapeutic gene AAV AAV vectors Zinc Finger Nuclease (ZFN) 1 and 2 Therapeutic gene - Single treatment - Can provide long lasting benefit - Single vector - Episomal therapeutic transgene with liver specific promoter - Treatment strategy is in clinic for Hemophilia Liver produces and secretes therapeutic enzyme with glycosylation suitable for tissue uptake and lysosomal delivery - Single treatment - Can provide life-long benefit - Three vectors - Integrated therapeutic transgene using albumin promoter - Treatment strategy is entering clinic for both MPS I and MPS II 9

cdna gene therapy strategy for Fabry Disease cdna gene therapy AAV vector Therapeutic gene Liver Cell Nucleus Promoter Proof of concept study design Single injection of cdna vectors into GLAKO mice cdna dose: 2e12 Vg/kg Weekly plasma collection and α-gal A activity measurement Takedowns at 2 months post-aav injection for tissue analysis GLAKO mouse accumulates Gb3 and lyso-gb3 in tissues Therapeutic Gene Liver Cell DNA Gb3 content WT 25 weeks GLAKO 25 weeks GLAKO Episomal therapeutic transgene with liver specific promoter WT WT WT WT liver kidney heart plasma 10

n m o l/h r/m l AAV-mediated delivery of optimized GLA cdna in GLAKO mice α-gal A activity in plasma α-gal A activity in tissues (2 months) 5 0 0 0 1 0 0 0 1 0 0 1 0 100x wild type 10x wild type wild type GLAKO wild type original cdna optimized 10x wild type 1 GLAKO liver heart kidney spleen 0.1 0 2 0 4 0 6 0 tim e (d a y s ) Original GLA cdna construct at low dose (2e12 vg/kg) Optimized GLA cdna construct at low dose (2e12 vg/kg) a-gal A overproduced in liver is safe, secreted at high levels and taken up by other tissues in active form

% Gb3 remaining % lyso-gb3 remaining Analysis of Gb3 and Lyso-Gb3 substrate clearance in target tissues Gb3 in tissues plasma liver heart Lyso-Gb3 in tissues plasma liver heart all samples <LLOQ 50% remaining 25% remaining 10% remaining 25% remaining 10% remaining untreated original optimized GLAKO treated GLAKO WT untreated original optimized GLAKO treated GLAKO WT a-gal A produced in liver leads to significant Gb3 and Lyso-Gb3 reduction in plasma, liver and heart

% Gb3 remaining Analysis of Gb3 and Lyso-Gb3 substrate clearance in target tissues Gb3 in tissues Lyso-Gb3 in tissues 1 0 0 plasma liver heart kidney 1 0 0 plasma liver heart kidney 7 5 7 5 5 0 5 0 2 5 2 5 10% remaining 10% remaining 0 G L A K O Untreated GLAKO G L A K O G L A K O G L A K O s p a c e r a-gala 100x WT s p a c e r 2.5 e 1 3 2.5 e 1 3 2.5 e 1 3 2.5 e 1 3 Treated GLAKO s p a c e r W T WT mice W T W T W T 0 G L A K O Untreated GLAKO G L A K O G L A K O G L A K O s p a c e r a-gala 100x WT Treated GLAKO 2.5 e 1 3 2.5 e 1 3 2.5 e 1 3 2.5 e 1 3 s p a c e r W T WT mice W T W T W T a-gal A produced in liver leads to significant Gb3 and Lyso Gb3 reduction in target tissues heart and kidney.

a-gal A activity (nmol/hr/ml) n m o l/h r/m l Evaluation of long-term a-gal A liver expression and efficacy α-gal A activity in plasma 50x WT 1 0 0 1 0 1 6 dose 5 e 1 2 groups 2 e 1 2 1 e 1 2 5 e 1 1 wild 2.5 etype 1 1 1.2 5 e 1 1 W T G L A K O GLAKO range 0 2 0 4 0 6 0 8 0 1 0 0 1 2 0 1 4 0 1 6 0 1 8 0 d a y s p o s t-a A V 2 /6 in je c tio n a-gal A overexpression from the liver is stable up to ~ 6 months and is well tolerated 14

In vivo genome editing strategy for Fabry Disease : Proof of concept study design In vivo genome editing Single injection of ZFNs and hgla transgene into GLAKO mice Total dose: 6e13 Vg/kg Strong albumin Promoter AAV vectors Zinc Finger Nuclease (ZFN) 1 and 2 Therapeutic gene Regular plasma collection and α-gal A activity measurement Albumin locus Takedowns at 2 months post-aav injection for tissue analysis H TG H Therapeutic gene Homology arm GLAKO Integration of therapeutic transgene at the albumin locus leads to potentially life-long stable expression 15

ZFN-mediated integration of hgla cdna at the albumin locus SP SP Signal peptide 16

n m o l/h r/m l In vivo genome editing leads to high α-gal A expression in plasma and uptake in secondary tissues α-gal A activity in plasma α-gal A activity in tissues (2 months) 1 0 0 0 0 1 0 0 0 SP2 1 0 0 SP1 1 0 1 wild type GLAKO 0.1 0 2 0 4 0 6 0 days post-aav tim e (dtransduction a y s ) liver heart kidney spleen Average: plasma 300x wild type heart 31x wild type kidney 2.3x wild type plasma 21x wild type heart 5.5x wild type kidney 0.5x wild type a-gal A produced from the albumin locus is secreted at high levels and taken up by other tissues in active form

a-gal A produced from the albumin locus has the appropriate glycosylation mediating cellular and lysosomal uptake Human α-gal A western in liver PNGaseF - - + - - + - - + - - + - - + Endo H - + - - + - - + - - + - - + - 50 kd 37 kd GLAKO treated (SP2) WT GLAKO Rec. a-gal A antia-gal A 18

% substrate remaining Analysis of Gb3 and Lyso-Gb3 substrate clearance in target tissues plasma liver heart kidney Gb3 lyso-gb3 untreated treated wild type untreated treated wild type GLAKO GLAKO GLAKO GLAKO (SP1) (SP1) 10% remaining α-gal A secreted by liver and taken up by heart and kidney is able to clear nearly all of the substrate in these tissues within 2 months 19

Conclusions Transducing GLAKO (Fabry) mice with either hgla cdna vectors or in vivo genome editing vectors led to: Expression of very high levels of α-gal A in the liver Secretion of functional α-gal A into the bloodstream resulting in stable plasma α-gal A activity levels many-fold above wild type Uptake of α-gal A by secondary tissues, leading to α-gal A activity exceeding wild type levels in the heart and spleen at the used doses H TG H Clearance of most or all of globotriaosylceramide (Gb3) and globotriaosylsphingosine (lyso-gb3) substrates in plasma, liver, heart and kidney 2 months after cdna gene therapy or genome editing These data support the development of Sangamo Therapeutics liver-based AAV approaches as potential therapies for the treatment of Fabry disease 20

Acknowledgments Robert Desnick, M.D-Ph.D Makiko Yasuda, M.D-Ph.D Silvere Pagant, Ph.D Marshall Huston, Ph.D Susan St. Martin Yolanda Santiago Scott Sproul Tanja Meyer, Ph.D Russell DeKelver, Ph.D Kathleen Meyer, M.P.H., Ph.D., D.A.B.T. Richard Surosky Daniel Richards Alicia Goodwin Edward J. Rebar, Ph.D Lisa King Michael C. Holmes, Ph.D 21