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MEMPHASYS LIMITED. — Investor Presentation 2007
Aug 23, 2007
65314_rns_2007-08-23_56543885-f6cd-4a0d-b65b-da9b6a4d01d7.pdf
Investor Presentation
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FOR IMMEDIATE RELEASE
The Hon. Tony Abbott MHR Opens NuSep’s Head Office and Business Presentations
SYDNEY, AUSTRALIA – 24 August 2007 – NuSep Ltd (ASX: NSP) is pleased to announce that the Minister for Health and Ageing, The Hon. Tony Abbott MHR officially opened NuSep’s Head Office at Frenchs Forest on Thursday 23 August.
The event was attended by many shareholders and invited guests.
As part of this function, guests were updated on the business operations, attached are the 3 presentation;
-
1] Update on the NuSep business by Mr John Manusu CEO of NuSep.
-
2] Update on the Sperm Sorter project by Prof John Aitken, Director, ARC Centre of Excellence in Biotechnology and Development, University of Newcastle.
-
3] Update by Dr Brad Walsh on the Diagnostic Kits for Prostate Cancer and Diabetes being developed by Minomic International.
NuSep has recently made a strategic investment in Minomic International and now has 16.5% shareholding in Minomic.
About NuSep Ltd
NuSep is an Australian BioSeparations company based in Frenchs Forest, Sydney. NuSep manufactures and markets a range of products to BioSeparations customers located worldwide through distribution and sales centres located in Australia, the USA and Europe. NuSep is listed on the Australian Stock Exchange where its shares trade under the code “NSP”.
NuSep currently operates across three product groups, each addressing BioSeparations customers, utilising patented technology and leveraging the company’s global distribution network. The three product groups are as follows:
-
Electrophoresis gels – NuSep offers two pre-cast gel ranges: iGels, innovative gels including long-life gels and gels with solid well dividers; and NuBlu, high quality gels at an every day price together with associated consumables.
-
Gradiflow[®] Instruments – NuSep has developed two unique laboratory separation devices based on Gradiflow[®] technology. The first to be released in early 2008 is a proteomics instrument that can separate a biological sample into eight fractions. The second instrument will be applied to sperm separation required for fertility treatments such as IVF.
22 Rodborough Road � Frenchs Forest NSW 2086 � Australia � 61.2.8977.9000 � 61.2.8977.9099 fax NuSep Ltd ABN: 33 120 047 556
www.nusep.com
– 2 –
Development of this product is supported by the Australian Government’s Commercial Ready program.
- Biological Products – NuSep supplies research grade reagents purified from human and animal plasma. The first product, human IgG was released in May 2007.
For more information about NuSep please visit the company’s website www.NuSep.com
Enquires/Additional information:
NuSep Ltd Prakash Patel Company Secretary (02) 8977 9000
# # # #
NuSep Business Outlook Mr John Manusu, CEO
Goal
To be the leading supplier to the BioSeparations market by providing products which lead the industry in terms of customer defined benefits
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Achievements since Floating
-
Establishment of direct global distribution
-
Launch of NuBlu Gels in the US
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Expanded sales force
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Launch of first biological reagent
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Sperm Sorter enters clinical trials
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Manufacturing and marketing rights for a prostate diagnostic kit
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Short Form Prospectus
Growth Strategy
-
Seeking growth through acquisition of products and/or companies
-
Acquisition must fit with present business:
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- Relevant to Life Science market
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- Compliment NuSep technology and capabilities
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- Compatible with distribution system
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- Offer revenue growth
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- Target monoclonal antibodies
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Why Monoclonal Antibodies?
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Rapidly growing market – set to double in next 5 years
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• Aggregate sales $US14b in 2005 (36.5% increase since 2004)
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NuSep to target reagent market worth $US450m
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mAb Market
Diagnostic
20%
Reagents NuSep Target
3%
Therapeutic
77%
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What are Monoclonal Antibodies (mAbs)?
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Antibodies that that can replicated endlessly
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High purity and specificity
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Able to recognise and bind to a specific antigen (eg. virus)
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Used for:
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Biomedical research
-
Disease diagnosis
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Treatment of illness (eg. infections, cancer)
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Future Direction
-
First deal mAbs based product (in-license of prostate diagnostic kit)
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Seeking additional opportunities
-
Targets assessed on following factors:
-
Profitability
-
Product portfolio and customer profile
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Novel manufacture
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Synergies with NuSep
-
Cashflow positive
Thank you
Cell Isolation Procedures for Human Spermatozoa
A joint venture with NuSep
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Cell Isolation Procedures for Human Spermatozoa
One in six Australian couples is affected by infertility
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Ovulatory Failure
Idiopathic
Tubal Damage
Coital
Endometriosis
Mucus dysfunction
Male factor
Hull et al., 1985
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At least one in twenty Australian males is infertile
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Assisted Reproductive Technology (ART) in Australia
41,000 ART cycles begin in Australia annually.
One in 25 Australian babies born this year will have been conceived through ART
The more of one generation you treat with ART the more the next generation will require ART
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Cell Isolation Procedures for Human Spermatozoa
One in 50 babies born through ART in Australia is stillborn or dies within a month of birth — twice the rate of babies conceived naturally.
Children conceived with ART also have about twice the risk of having a major birth defect or low birth weight than children conceived naturally
Nature’s barriers to fertilization by defective spermatozoa are circumvented
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DNA Damage in Sperm of Donors and Patients
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55
Comet assay
50
45
40
35
30
25
20
15
10
5
Donor Patient
Median tail DNA
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Reproductive consequences of DNA damage in the male germ line
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Impaired fertilization (Benchaib et al., 2003; Virro et al., 2004;
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Aitken 2004)
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-
Disrupted preimplantation development (Sakkas et al.,
-
1998; Morris et al., 2002; Virro et al., 2004).
-
Increased rates of abortion (Saleh et al., 2003; Carrell et al.,
-
2003).
-
Increased rates of disease in children and young
-
adults (Ji et al., 1997; Aitken and Krausz, 2001; Aitken, 2004).
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DNA damage and Achondroplasia
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Achondroplasia
5 n = 152
r = 0.56; P< 0.0001 6.0
4
4.0
3
2
2.0
1
0
0
20 25 30 35 40 45 50 55 60
22 32 42 52
Paternal Age Paternal Age
Relative frequency (/100,000)
Log percent highly damaged DNA
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Impact of paternal age on Autism
Reichenberg et al. Arch Gen Psychiatry (2006) 63 1026-1032
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10
8
6
4
*
2
Reference
0
15-29 30-39 40-49 50+
Odds Ratio
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Paternal age (yrs)
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Factors capable of inducing DNA damage in the male germ line
| Smoking | Hexachlorocyclohexane | Cryptorchidism |
|---|---|---|
| Alcohol | Trinitrotoluene | Testicular torsion |
| Chromic acid | Aflatoxin | Diabetes |
| Iron | Lindane | Hyperthyroidism |
| Lead | Adriamycin | Varicocele |
| Cadmium | Cisplatin | Infection |
| Uranium | Quinalphos | Physical exertion |
| Arsenic | Endosulfan | Hypogonadotrophism |
| Vanadate | Diethyl maleate | |
| Phthalate esters | Monensin | |
| Sulfur dioxide | Formaldehyde | |
| Sodium fluoride | Alloxan | |
| PCB/PCN | Streptozotocin | |
| Methoxychlor | Ozone | |
| Bisphenol A | Retinoids | |
| Nonylphenol | ||
| Cyclophosphamide |
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Smoking and DNA damage to human sperm
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DNA fragmentation Oxidative damage to DNA
12
10
Sun et al. (1997) Biol
Fraga et al (1996) Mut
Reprod 58: 602-607 Res 351: 199-203
10
8
5
6
4
0
2
Smoker Non-Smoker Smoker Non-Smoker
n = 35 n = 78 n = 22 n = 22
on (%)
NA Fragmentati
D Oxo8 dG (fmol/mg DNA)
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Impact of smoking on Childhood Cancer
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Cancer
All tumours
Brain
Ji et al., 1997
Lymphoma
ALL
0 1 10
OR 95%CI
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Sperm Sorter System Schematics – Sperm Cell Separation
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Electrophoretic sperm isolation
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30
P < 0.001
25
20
15
10
5
0
30 60 120 300 600 900
Duration of electrophoresis (sec)
/ml)
6
Sperm concentration (10
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Electrophoretic isolation of spermatozoa
Reduction in DNA damage
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Separated
TUNEL
Residual
20 40 35
35
30
15 30
25
25
20
10 20
15
15
10
5 10
5
5
0
Snap Frozen Cryopreserved Biopsy
TUNEL positive (%)
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Case Study
-
Couple exhibiting long-term infertility (10+years) associated with high levels of DNA damage in the male germ line. Patient produced an oligozoospermic ejaculate containing 3.2 million spermatozoa/ml and an equivalent number (2.1 million/ml) of contaminating round cells.
-
Pre-separation:
30% vitality 18% motility DNA damage - 26% TUNEL positive, 41% SCSA DFI
- Post-separation:
62% vitality 24% motility DNA damage - 14% TUNEL positive, 15% SCSA DFI
-
Intracytoplasmic sperm injection (ICSI) was conducted using the electrophoretically isolated spermatozoa.
-
Oocytes were fertilized and normal blastocysts were generated after 5 days of culture. Transfer of two embryos was associated with the generation of a positive hCG signal followed by confirmation of a viable pregnancy by ultrasound.
-
This is the first clinical report of a viable pregnancy following the electrophoretic isolation of spermatozoa
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A collaboration with Sydney IVF
Intrauterine insemination
Intrauterine insemination is an effective first line treatment in properly selected cases and is less invasive than in vitro fertilisation and its variants.
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Buffer flow
Cathode (-ve terminal)
Innoculation chamber (1.8 ml)
Separation membrane
Collection chamber (0.4 ml)
Anode (+ve terminal)
Buffer flow
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Sperm Cell Separation
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Asymmetrical - IUI
Buffer flow
Cathode (-ve terminal)
Innoculation chamber
Separation membrane
Collection chamber
Anode (+ve terminal)
Buffer flow
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Symmetrical - IVF and ICSI
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Aus Industry
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Protein Digest
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Prefractionation
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