NeuroScientific Biopharmaceuticals Ltd - Novel drug therapies for neurodegenerative conditions - Ausbiotech Investment
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DISCLAIMER The purpose of the presentation is to provide an update of the business of NeuroScientific Biopharmaceuticals Ltd (“NeuroScientific”, or “the Company”). These slides have been prepared as a presentation aid only and the information they contain may require further explanation and/or clarification. Further information is available upon request. The views expressed in this presentation contain information derived from publicly available sources that have not been independently verified. No representation or warranty is made as to the accuracy, completeness or reliability of the information. Any forward looking statements in this presentation have been prepared on the basis of a number of assumptions which may prove incorrect and the current intentions, plans, expectations and beliefs about future events are subject to risks, uncertainties and other factors, many of which are outside NeuroScientific’s control. Important factors that could cause actual results to differ materially from assumptions or expectations expressed or implied in this presentation include known and unknown risks. Because actual results could differ materially to assumptions made and NeuroScientific’s current intentions, plans, expectations and beliefs about the future, you are urged to view all forward looking statements contained in this presentation with caution. This presentation should not be relied on as a recommendation or forecast by NeuroScientific. Nothing in this presentation should be construed as either an offer to sell or a solicitation of an offer to buy or sell shares in any jurisdiction.
3 CORPORATE OVERVIEW ▹ Completed IPO listing on the ASX Capital Structure on the 27 July 2018 ASX code NSB Shares on issue 73,580,592 ▹ Lead candidate funded through to completion of Phase I Price (close 29/10/2018) $0.165 Market cap $12.4M ▹ Pipeline of potential therapeutic Shares escrowed 12-months 1,906,269 candidates with strong IP protection Shares escrowed 24-months 19,349,506
4 BOARD & MANAGEMENT STEPHEN BRIAN LEEDMAN MATT LIDDELOW DR ANTON UVAROV QUANTRILL Co-founder of ResApp >12 years experience Founding director of 20 years’ experience in Health Ltd (ASX.RAP), commercialising medical Actinogen (ASX:ACW), corporate advisory and Imugene Ltd (ASX:IMU) devices and conducting the largest company directorship, and Oncosil Ltd pharmaceuticals for Alzheimer’s study in Executive Chairman of (ASX.OSL) Australian and multi- Australasia with 174 McRae Investments. national companies patients. Former analyst including AstraZeneca. with Citigroup, New York. Non-executive Chairman MD & CEO Executive Director Non-executive Director
5 COMPANY HIGHLIGHTS Advanced preclinical lead drug candidate with multiple treatment indications Strong strategic partnerships geared towards success Validated strategy and business model Experienced board and management team
6 TREATMENT MARKETS WITH UNMET NEED Alzheimer’s disease Optic nerve conditions 48M people globally have dementia 5% of population suffer vision loss due to 70% of dementias damaged optic nerve Alzheimer’s disease 60M people US $818B global affected by glaucoma economic burden
7 LEAD CANDIDATE: EMTINB NOVEL Modeled on MT-II protein Binds LRP-1 receptors – novel MOA Stops cell death & stimulates regeneration VALIDATED Preclinical in vitro models – successfully repeated Animal models MULTIPLE INDICATIONS MOA: LRP-1 receptor ubiquitous Not directly targeting a process of disease
8 EVOLUTION OF EMTINB MT-II Structure EmtinB Peptide EmtinB Peptide Dendrimer β-domain α-domain ▹ 61 amino acid length ▹ 14 amino acid length ▹ Synthesised as a ▹ Binds divalent metal ions ▹ Isolated from the β- dendrimer: ▹ Difficult to manufacture domain of MT-II protein Increased potency and stability
9 EMTINB MECHANISM OF ACTION: Binding LRP-1 receptor
10 EMTINB SCIENTIFIC DATA Preclinical studies Increased mean survival of Stimulates neurite brain cells >90% outgrowth by up to 300% Cell survival: 48-hour incubation period Neurite length: 24-hour treatment period EmtinB 92% EmtinB 225% Induced 64% Control 100% toxicity Control 100% 0% 50% 100% 150% 200% 250% 0% 50% 100 %
11 EMTINB SCIENTIFIC DATA Preclinical studies in AD models Prevented cell death in in vitro Slowed progression of disease Alzheimer’s model of toxicity (memory impairment) by >80% in Alzheimer’s animal model Control 100% Cognition: treatment for 48 days Aβ-42 50% EmtinB 70% +7 Control 38% +5 EmtinB 100% 0% 50% 100 0% 50% 100% %
12 SUPPORTING SCIENTIFIC DATA Regenerating the optic nerve ▹ Precursor to EmtinB (MT-II) stimulated regenerative growth of optic nerve after complete surgical transection Optic Nerve Growth Treatment No treatment
13 EMTINB DEVELOPMENT SCHEDULE 2018 2018 2019 2019 2019 2019 Q3 Q4 Q1 Q2 Q3 Q4 Alzheimer’s disease indication Preclinical safety & toxicology studies Additional AD animal efficacy study Phase I clinical study Ophthalmology indication Preclinical safety studies Preclinical efficacy studies Phase I clinical studies
14 STRATEGIC PARTNERSHIPS ▹ Partner for preclinical studies ▹ Partner for ophthalmology studies ▹ Managed >3300 unique compounds ▹ Developed 1st artificial cornea ▹ >500 IND/CTD programs in the last ▹ Developed 1st transgenic animal 5-years model for macular degeneration ▹ Offer complete development solution ▹ Glaucoma treatment recently from preclinical to clinical to market acquired by global pharma Allergan
15 DEVELOPMENT PIPELINE Preclinical Phase Clinical Phase Lead Animal Safety & Phase Ia Phase Ib optimisation efficacy toxicology Alzheimer’s disease EmtinB Degenerative conditions of the optic EmtinB nerve Other Emtin peptides
16 BUSINESS MODEL ▹ Company will seek to out-license EmtinB for late-stage clinical development ▹ Potential for multiple treatment indications will be attractive to “big pharma”
17 KEY MILESTONES Nov / DEC-18 FEB-19 Report on ocular tissue Results on additional distribution study in efficacy study in CVN rabbits. Alzheimer’s model JAN-19 APR / May-19 Results on efficacy study Expected conclusion of in glaucoma pig model safety & toxicity studies
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