Disease Modifying Therapy for DMD: Utrophin Modulation Programme

Similar documents
GT-020 Phase 1 Clinical Trial: Results of Second Cohort

DIAGNOSING CHILDHOOD MUSCULAR DYSTROPHIES

Overview of Phase 1 Oncology Trials of Biologic Therapeutics

Muscular dystrophy clinical manifestations: progressive proximal extremity weakness respiratory muscle weakness cardiomyopathy

Muscular dystrophy: basic facts

Biological importance of metabolites. Safety and efficacy aspects

Muscular Dystrophy: Stem Cell Therapy

2nd MuscleTech Network Workshop. From translational Research to translational Medicine. CONCLUSIONS AND CLOSING REMARKS Dr.

Clinical Study Synopsis for Public Disclosure

HUNTINGTON S DISEASE THERAPIES RESEARCH UPDATE

COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) NOTE FOR GUIDANCE ON THE PRE-CLINICAL EVALUATION OF ANTICANCER MEDICINAL PRODUCTS

Reflection paper on clinical aspects related to tissue engineered products

Not All Clinical Trials Are Created Equal Understanding the Different Phases

Session 6 Clinical Trial Assessment Phase I Clinical Trial

Serum Creatine Kinase analysis in mouse models of muscular dystrophy.

Medical Therapies Limited EGM Presentation

Statistics and Pharmacokinetics in Clinical Pharmacology Studies

Pharmacology skills for drug discovery. Why is pharmacology important?

Newsletter. WntResearch AB, Medeon Science Park, Per Albin Hanssons väg 41, Malmö, Sweden. Primary Objective:

Clinical Trial Results Database Page 1

Fexinidazole a new oral treatment for sleeping sickness update of development

JAK1 and beyond. Investor Presentation February Copyright 2013 Galapagos NV

Non-clinical development of biologics

Achieving Regulatory Success: Areas of focus for biotechnology companies. Michael J. Schlosser, PhD, DABT April 21, 2013

Week 12 study results

Exelixis Showcases R&D Pipeline at JPMorgan Healthcare Conference

A Phase 2 Study of HTX-011 in the Management of Post-Operative Pain Positive Top-Line Results

TGN 1412 Welche Änderungen haben sich für die Erstanwendung am Menschen aus Sicht des BfArM ergeben?

Lilly Covance Strategic Alliance From Vision to Results. Adrienne Takacs, PhD Jonathan Koch, MBA

Proof-of-Concept Studies and the End of Phase IIa Meeting with the FDA

Lead optimization services

Localised Cancer Treatment. PCI Biotech. Amphinex a new product for localised cancer treatment

Gene Silencing Oligos (GSOs) Third Generation Antisense

The Promise and Challenge of Adaptive Design in Oncology Trials

A Peak at PK An Introduction to Pharmacokinetics

Company Update. March 2011

Guidance for Industry

ESCMID Online Lecture Library. by author

NONCLINICAL EVALUATION FOR ANTICANCER PHARMACEUTICALS

BNC105 CANCER CLINICAL TRIALS REACH KEY MILESTONES CLINICAL PROGRAM TO BE EXPANDED

Summary of the risk management plan (RMP) for Orkambi (lumacaftor and ivacaftor)

FSH Society s 2014 Biennial FSHD Connect Meeting: Natural History Studies

JAK1 and beyond. Investor Presentation January Copyright 2014 Galapagos NV

CAN-FITE BIOPHARMA LTD.

Sheffield Kidney Institute. Planning a Clinical Trial

Q PRESENTATION February 9, 2016 Per Walday, CEO Ronny Skuggedal, CFO

Dec. 9, 2013, 11:00 a.m. EST

Galapagos reports largest cash balance ever

Rare Diseases: Common Issues in Drug Development Guidance for Industry

Delivering gene therapy to patients

Chapter 10. Summary & Future perspectives

GENERAL CONSIDERATIONS FOR CLINICAL TRIALS E8

Developing Innovative Therapeutics for People with Orphan Liver Disease

VITAMIN C AND INFECTIOUS DISEASE: A REVIEW OF THE LITERATURE AND THE RESULTS OF A RANDOMIZED, DOUBLE-BLIND, PROSPECTIVE STUDY OVER 8 YEARS

Duchenne muscular dystrophy

PARP inhibitors and TEMOZOLAMIDE in BRAIN TUMORS. Idoia Morilla Ruiz

M4E(R2): The CTD Efficacy

MOLOGEN AG. Q1 Results 2015 Conference Call Dr. Matthias Schroff Chief Executive Officer. Berlin, 12 May 2015

Teriflunomide is the active metabolite of Leflunomide, a drug employed since 1994 for the treatment of rheumatoid arthritis (Baselt, 2011).

Guidance for Industry

Effets biologiques des facteurs de croissance sur la régénération musculaire

MATHEMATICAL MODELS OF TUMOR GROWTH INHIBITION IN XENOGRAFT MICE AFTER ADMINISTRATION OF ANTICANCER AGENTS GIVEN IN COMBINATION

ICH Topic E 8 General Considerations for Clinical Trials. Step 5 NOTE FOR GUIDANCE ON GENERAL CONSIDERATIONS FOR CLINICAL TRIALS (CPMP/ICH/291/95)

How To Get A Grant From Kinesis

EVT Execute & EVT Innovate Leading drug discovery

Effective Outsourcing of Clinical Pharmacology Studies in Europe. John Horkulak Executive Director, Eurasian External Clinical Study Operations

Clinical Study Synopsis

FACT SHEET TESTETROL, A NOVEL ORALLY BIOACTIVE ANDROGEN

Clinical Trials and YOU

Stem Cell-based Therapies and FDA Regulations

Sanofi Reports Positive Phase 3 Results for Toujeo (insulin glargine [rdna origin] injection, 300 U/mL)

Corporate Booklet February 2016

Risk Assessment in Chemical Food Safety. Dept. of Food Safety and Zoonoses (FOS)

Abbott Nutrition. Attractive Profile and Compelling Growth Opportunities

Multiple Sclerosis in Practice. An Expert Commentary With Jeffrey Cohen, MD, PhD A Clinical Context Report

The Clinical Trials Process an educated patient s guide

WntResearch. Foxy-5 A unique Phase 1 opportunity to combat the spreading of cancer

First In Human Pediatric Trials and Safety Assessment for Rare and Orphan Diseases

Leveraging Biomarkers in Early Clinical Drug Development for Metabolic Disease Therapies. Mallé Jurima-Romet, PhD August 31, 2011

BAY , a novel ADC with potent anti-tumor activity, targeting all isoforms of FGFR2

New Advances in Cancer Treatments. March 2015

Careers in Biostatistics and Clinical SAS Programming An Overview for the Uninitiated Justina M. Flavin, Independent Consultant, San Diego, CA

a Phase 2 prostate cancer clinical trial is ongoing. Table 2: Squalamine vs Standard-of-care literature

ALPHA (TNFa) IN OBESITY

European Medicines Agency decision

Muscle Physiology and the. Pathology of Muscular Dystrophy

Guidance for Industry

Translation of Regenerative Medicine. Prof Trevor M Jones CBE

CLINICAL TRIALS SHOULD YOU PARTICIPATE? by Gwen L. Nichols, MD

COMMITTEE FOR VETERINARY MEDICINAL PRODUCTS GUIDELINE FOR THE CONDUCT OF POST-MARKETING SURVEILLANCE STUDIES OF VETERINARY MEDICINAL PRODUCTS

Basic Overview of Preclinical Toxicology Animal Models

Guidance for Industry Safety Testing of Drug Metabolites

Guidance for Industry

GUIDELINES FOR THE TREATMENT OF DIABETIC NEPHROPATHY*

5 Frequently Asked Questions About Adult Stem Cell Research

ICH Topic S 1 A The Need for Carcinogenicity Studies of Pharmaceuticals. Step 5

VERTEX PHARMACEUTICALS INC / MA

Longitudinal Modeling of Lung Function in Respiratory Drug Development

Freiburg Study. The other 24 subjects had healthy markers closer to what would be considered ideal.

Transcription:

Disease Modifying Therapy for DMD: Utrophin Modulation Programme PPMD Connect, June 2014

Legal Disclaimer FORWARD-LOOKING STATEMENTS This Document contains forward-looking statements. These statements relate to, among other things, analysis and other information that are based on forecasts of future results and estimates of amounts not yet determinable. These statements also relate to the Company s future prospects, developments and business strategies. Forward-looking statements are identified by their use of terms and phrases such as believe, could, envisage, estimate, expect, intend, may, plan, will or the negative of those, variations or comparable expressions, including references to assumptions. The forwardlooking statements in this Document are based on current expectations and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by those statements. Given the risks and uncertainties associated with a company of this nature, potential investors should not place reliance on forward-looking statements. These forward-looking statements speak only as at the date of this Document. The Company does not undertake any obligation to update forward-looking statements or risk factors other than as required by any relevant regulations, whether as a result of new information, future events or otherwise. 2 PPMD Connect June 2014

Dystrophin or Utrophin Protein: Maintaining Integrity of Muscle Fibres Muscle fiber membrane Extracellular matrix Actin cytoskeleton Dystrophin or Utrophin Dystrophin or utrophin protein 3 PPMD Connect June 2014

Utrophin Modulation: A Disease-Modifying Approach for DMD Utrophin is functionally equivalent to dystrophin in both fetal and repairing muscle Utrophin is continually expressed at specialized sites in normal mature muscle fibers Normal Fiber Fetal (repairining) Time to Develop Fetal/ Immature Mature Utrophin modulation is a diseasemodifying strategy of potential utility for all DMD patients (independent of dystrophin mutation) DMD Fiber Degeneration Only normal utrophin levels required for DMD muscle recovery SMT C1100 designed to increase and maintain utrophin transcription DMD + SMT C1100 Fiber utrophin dystrophin 4 PPMD Connect June 2014

SMT C1100 Increased Utrophin Levels in Muscle Fibers Improves Disease Biomarkers In Vivo Reduced Fiber Regeneration (%CNFs) extensor digitorum longus tibialis anterior Reduced Muscle Leakiness (blood CK levels) mdx mdx + SMT C1100 Increased utrophin at the sarcolemma significantly reduces secondary disease effects 28 days of oral dosing (50mk/kg, QD) in mdx mice (n=5) Source: PLoS ONE, Vol 6, Issue 4, May 2011 mdx vehicle mdx+smt C1100 5 PPMD Connect June 2014

UTROPHIN MODULATION PROGRAMME Clinical Data 6 PPMD Connect June 2014

Summary of Phase 1 Healthy Volunteer Trial Repeat dose Phase 1 healthy volunteer trial conducted in 2012 showed SMT C1100 was safe and well tolerated at all doses tested Achieved levels expected to increase utrophin expression for at least 14 hours/day Higher plasma levels achieved when SMT C1100 taken with food SMT C1100 taken with food v SMT C1100 taken after 12h fasting (same individuals after washout) 200mg/kg 7 PPMD Connect June 2014

Phase 1b Trial: Overview UK-based study 4 sites: London, Liverpool, Birmingham, Manchester 12 ambulatory DMD patients aged 5 to 11 years old 3 escalating dose cohorts, 4 patients per cohort: 50mg/kg BID, 100mg/kg BID, 100mg/kg TID 10 days of oral dosing Dosing to occur ideally within 10 minutes of consuming food Primary endpoint: Tolerability & Safety Secondary endpoint: PK levels of SMT C1100 and metabolites 8 PPMD Connect June 2014

Phase 1b Trial: Safety and PK First ever utrophin modulator trial in patients Safety: Primary endpoint of trial achieved SMT C1100 safe and well-tolerated in patients at all doses tested No apparent issues with patient compliance Variable Plasma levels of drug 2/12 boys had good SMT C1100 plasma levels appropriate for activating utrophin modulation 10/12 boys plasma levels were similar to fasted healthy adult volunteers 9 PPMD Connect June 2014

Phase 1b Trial: CK Observation Reduction in enzyme related to muscle damage Serum creatine kinase (CK) is an enzyme associated with muscle fibre damage and serum levels are elevated in DMD patients Reduced serum CK levels seen in non-clinical efficacy studies in mdx model after 15 days treatment with SMT C1100 Phase 1b data CK levels were reduced during dosing in the majority of boys Result is consistent with mdx data Consistent with reduction in muscle membrane damage 10 PPMD Connect June 2014

Next Steps: Targeting all Patients with DMD Future clinical trials of SMT C1100 to be modified to reflect our greater understanding of the importance of diet and other potential disease related factors Will seek to determine the optimal way to address drug exposure variability Dietary means and/or Drug formulation change Formulations already identified that increase exposure in animal studies Next patient study now expected to start in Q4 2014 11 PPMD Connect June 2014

12 PPMD Connect June 2014

13 PPMD Connect June 2014

Alliance represents a multi-year strategic collaboration that combines extensive utrophin biology, chemistry and drug discovery expertise Commitment to build on the results obtained with SMT C1100 Aim to deliver first in-class and best in-class utrophin modulators for the therapy of DMD 14 PPMD Connect June 2014

Utrophin Modulation Programme Lead: SMT C1100 SMT C1100 related Next Generation DISCOVERY OPTIMISATION PRECLINICAL PHASE 1 PHASE 2 15 PPMD Connect June 2014

UTROPHIN MODULATION PROGRAMME Next Generation and Biomarkers 16 PPMD Connect June 2014

Next Generation Utrophin Modulators 1. Structurally Related to SMT C1100 Similar in vitro potency to SMT C1100, enhanced PK properties Clean safety/off target profile Rat In vivo PK Study 2. New structures, new mechanism New screening technology identifying differentiated utrophin modulators Potential new mechanism of action Increased in vitro activity compared to SMT C1100 Utrophin Levels in DMD patient Myoblasts 17 PPMD Connect June 2014

Biomarker Development Programme Utrophin / Mechanism Related UTRN localisation by quantitative IF UTRN mrna by QPCR UTRN protein by MS/MS Muscle Health From Muscle: Regeneration markers Inflammatory markers From Sera: Membrane damage (muscle enzymes, MicroRNAs) Active fibrosis (collagen fragments) Non-invasive Markers Muscle MRI 18 PPMD Connect June 2014

Thank You to the Community 19 PPMD Connect June 2014

Contact If you have further questions, do get in contact: Email: dmd@summitplc.com Phone: +44 (0)1235 44 39 39 Web: Twitter: @summitplc 20 PPMD Connect June 2014