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CYCLOPHARM LIMITED AGM Information 2017

May 8, 2017

64741_rns_2017-05-08_81451223-2b60-4095-b924-3efd0286e8b3.pdf

AGM Information

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Cyclopharm Limited

2017 Annual General Meeting

9 May 2017

1

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2017 AGM

Chairman’s Address David Heaney

2

Our Strategy

CYC has a clear strategy to leverage our position as a leading player in the global nuclear medicine imaging market and lung health space to expand the use of our proprietary products and introduce new innovative technology.

We will do this by:

1. Attaining approval to distribute Technegas in the USA

2. Expanding the use of Technegas beyond the traditional diagnosis of Pulmonary Embolism into significantly larger applications such as COPD1 and Asthma, Lung Cancer and Pulmonary Hypertension for both diagnosis and patient management.

3. Identifying, developing and commercialising complementary innovative technology such as Ultralute[TM]

4. Leveraging our core global regulatory strengths, fiscal discipline, strong balance sheet and well developed expertise in nuclear medicine and pulmonary healthcare to seek out complementary technologies and businesses

3

  1. COPD‐Chronic Obstructive Pulmonary Disease

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2017 AGM

Managing Director’s Review

James McBrayer

  • Company Overview – Our Business

  • Investment Highlights

  • CYC’s 10 Fast Facts

  • Our Strategy

  • 2016 Achievements

  • 2016 Financial Results and Performance

  • Product Overview and Growth Opportunities

  • Technegas

  • Ultralute

  • 2017 Strategic Priorities and Outlook

4

Our Business….

Business Model Based on Annuity Stream From Consumables

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Manufacturer and distributor of lung ventilation imaging devices and equipment

  • Invented in 1986

  • Track record of growing revenue, profits and cash flows

  • USFDA trials for sales in US progressing

  • Functional ventilation imaging agent used predominantly in the diagnosis of Pulmonary Embolism (PE)

  • Preliminary China trials indicate that

  • Technegas can be an effective tool to diagnose and monitor COPD

  • Active clinical program underway targeting indication expansion

  • Revenues derived from:

    • Technegas Generator

Technegas

  • Patient Administration Set (Single patient consumable sold in boxes of 50)

  • Service Income

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Innovative, first-in-class, disruptive, proprietary technology used to improve radiopharmaceutical manufacturing efficiency and deliver health care cost effectiveness

  • Fine tuning in 2016

  • IP Secured

  • First sales expected in 1H 2017

  • Strong International interest as demonstrated by the International Atomic Energy Agency

  • Revenues derived from:

  • Cartridge shielding – one off sale per site

  • Disposable cartridges

5

Investment Highlights – Record Results

CYC is a leading player in the global nuclear medicine imaging and lung health markets

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$
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  • Technegas : Diagnosis & monitoring of lung diseases

  • Ultralute[TM] : Extends useful life of medical isotopes

2016 Sales : A$14.4 million  14.3% • 2016 EPS : 1.63 cents (81%)

  • 2016 EPS :

A$46.5 million 22.7%

  • :

  • Market Cap

  • 12 month TSR :

Market data source: ASX, Factset

6

12 month Total Shareholder Return = Share price + Dividend return for 12 months to 1 May 2017

CYC’s 10 Fast Facts

  1. Technegas is a well-established proprietary world leader in functional lung ventilation imaging technology with an annuity style product and service revenue streams with the majority of sales generated from single patient consumables.

  2. Technegas is already being sold in 56 countries with significant expansion opportunities in the USA following USFDA approval of Phase 3 clinical trials and the prospect of FDA approval by mid-2018

  3. Chronic Obstructive Pulmonary Disease (COPD) and asthma represent tremendous opportunities for substantial Technegas growth worldwide

  4. Ultralute[TM] , a new, innovative technology with global application, is being commercialised in 1H 2017

  5. Ultralute[TM] technology is also a platform for additional product development

  6. We benefit from deep experience across the management team and workforce

  7. Cyclopharm recorded another excellent financial result in 2016 with good foundations for growth: an increase of $1.8 million sales. We have a strong balance sheet with $4.59 million in cash at 31 December 2016

In summary, in 2016 we were an Australian Biotech that:

  1. Profitable, generating cash, debt-free and paid dividends.

  2. Maintained net cash on the balance sheet to fund growth; and

  3. Positioned to leverage transformational growth opportunities.

7

Our Strategy

CYC has a clear strategy to leverage our position as a leading player in the global nuclear medicine imaging market and lung health space to expand the use of our proprietary products and introduce new innovative technology.

We are doing this by:

1. Attaining approval to distribute Technegas in the USA

2. Expanding the use of Technegas beyond the traditional diagnosis of Pulmonary Embolism into significantly larger applications such as COPD1 and Asthma, Lung Cancer and Pulmonary Hypertension for both diagnosis and patient management.

3. Identifying, developing and commercialising complementary innovative technology such as Ultralute[TM]

4. Leveraging our core global regulatory strengths, fiscal discipline, strong balance sheet and well developed expertise in nuclear medicine and pulmonary healthcare to seek out complementary technologies and businesses

Our unremitting focus on these priorities delivered solid financial results in 2016, supporting further investment in growth opportunities and dividend payments to shareholders

  1. COPD‐Chronic Obstructive Pulmonary Disease

8

2016 Achievements

  • FY2016 Sales of $14.39 million

FY2016 EBIT $1.44 million

  • Payment of recurring dividends

  • Cash reserves at 31 December totalling $4.59 million after repayment of debt & relocation

  • USFDA clinical trial program on track (time & budget)

  • Decision to move forward with the USA expansion strategy independently

  • Preliminary results of trials in China show Technegas can be an effective tool used to diagnose and monitor COPD

  • Ultralute[TM] – Patent protection secured and commercialisation advanced

  • New Generation Technegas Generator project takes shape

  • Relocation of manufacturing facility to meet the growing global demand

  • China strategy paying dividends with single largest Technegas order valued at $1.3 million delivered December 2016

  • Global strategic partnerships under development, including Five Year Collaborative Agreement signed with the Canadian Association of Nuclear Medicine

9

2016 Financial Results and Performance

Year ended 31 December ($000’s) 2016 Change 2015 Change 2014
Sales Revenue
PAS 10,782 6.3% 10,145 8.1% 9,384
Generators/service 3,604 52.5% 2,363 12.2% 2,106
Total Sales 14,386 15.0% 12,508 8.9% 11,490
Underlying EBITDA 3,438 15.4% 2,980 13.0% 2,638
Underlying EBITDA Margin 23.9% 0.2% 23.7% 0.7% 23.0%
FDA Expenses (1,098) 60.0% (686) 43.5% (478)
EBITDA 2,340 2.0% 2,294 6.2% 2,160
D&A (106) 22.6% (137) 38.6% (223)
EBIT 2,234 3.6% 2,157 11.4% 1,937

Underlying Results represent results from the Technegas Division excluding one off items (Insurance settlement and costs/lease termination and double rent period costs) and FDA expenses.

  • Another record financial result in FY16

  • Underlying strong financial performance supports ongoing investment in R&D and costs associated with expansion into new markets and indications

  • A third consecutive year of record revenues in FY2016 assisted by the delivery in December 2016 of the single largest order placed for the China market

10

Cyclopharm Group Balance Sheet

($000’s) FY 2016 FY 2015 FY 2014
Cash 4,591 6,445 3,268
Other current assets 6,470 6,653 5,582
Non-current Assets 5,354 3,443 2,111
Total Assets 16,415 16,541 10,961
Current Liabilities 3,896 3,176 2,874
Borrowings - 197 246
Non-current Liabilities 57 66 85
Total Liabilities 3,953 3,439 3,205
Net Assets 12,462 13,102 7,756
  • Operating cash flows supported $1.5m Kingsgrove HQ capex, $0.43m one-off relocation costs, ongoing USFDA trials and recurring dividends

  • Capacity to fund growth initiatives and ongoing R&D

  • Medium to long term future of the Cyclopet facility at Macquarie University under consideration - includes possible divestment and partnerships

  • Debt free – Mortgage Debt retired in March 2016

11

Technegas – A Global Success Story

  • Technegas sold in 55 countries

  • Europe is the largest regional market for Technegas

  • In 2014 Canada became largest country market for Technegas, surpassing France

  • Over 210,000 patient studies in 2016

  • Over 3,500,000 patient studies since 1986

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  • 1,500 Technegas generators sold globally

  • Expanding operations in North America pending completed clinical trials and FDA approval

  • Expanding the use of Technegas – China COPD trial completed in 2016

  • Expansion of clinical development program in 2016 and 2017

  • Patent protection until 2026 with optionality for extension

  • 75% of sales are from single patient consumables / patient administration sets (PAS)

12

Technegas – USFDA Approval Within Reach

USA Market Size:

  • Half the world’s nuclear medicine departments are in the USA

  • USA represents a potential base Pulmonary Embolism market of 480,000 patients per annum. (Current Rest of the World volumes = 200,000 patients per annum)

Study Specifics:

  • Non-inferiority structural ventilation study comparing Xe133 vs. Technegas

  • Pathway to approval requires a two part study (CYC 010 & CYC009)

  • CYC 010 – Establishes the Inter & Intra reader variability for Xe133 – Completed

  • CYC 009 - Compares Xe133 with Technegas requiring patient recruitment – SPA Approved & Clinical Trial Underway

  • “All Comers” protocol to eliminate previous obstacles in patient recruitment

  • Total estimated trial cost < $7 million USD with $1.1 m AUD spent in 2016

  • Assumes 240 patient study at 10 clinical sites

  • CYC has decided at this stage to independently proceed in funding the trial

TIMELINE

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1H 2016 2H 2016 1H 2017 1H 2018 H1 2018 H2 2018
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Commence Finalise CYC 010 Commence Submit 1[st] Finalise Submit Clinical Targeted USFDA CYC 010 Submit CYC 009 CYC 009 40 patients CYC 009 Trial Results for Approval for SPA for Review Recruitment USFDA Review Approval

13

Ultralute[TM] The Next Phase of Growth

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Product Overview Technical Features
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  • Disruptive Technology – changes 60 years of how radiopharmaceuticals are manufactured

  • Enables a user to extend the usable life of a Mo99 Generator

  • Extends the effective use of Mo99 generator up to 50%

  • Allows the user to purchase a smaller (lower cost) Mo99 Generator

  • Each cartridge consumable designed for a maximum of 5 uses

  • Provides greater flexibility and product optimisation in manufacturing radiopharmaceuticals

  • Patents secured in 2014

  • Provides a saving of between 30% to 40% in the cost of Tc‐99m

  • Will be designated as laboratory equipment

  • Market introduction represents a base platform for additional applications

  • Enhances radiolabelling efficiency and imaging quality

  • Revenues commencing 1H 2017

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  • Purifies contaminants from the Tc99m eluate

  • Strong support from the International Atomic Energy Association (IAEA) where they refer to Ultralute[TM] as“a new innovation…that has significant global potential in the nuclear medicine supply chain”.

  • Provides a platform for further product development

14

Ultralute[TM] Generational Overview & Mo99 Supply Chain

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Molybdenum Manufacturing and Supply Chain
Hospitals/Clinics
U235 & Radiopharmacies
Targets
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  • Designed for the end user application

• Introduced to market Q4 2015 with revenues commencing GEN 1 1H 2017

  • Designed for radiopharmacy application

  • GEN 2 Development commenced in 2016 for 2018 launch

  • Concept to target Mo99 production via n,Gamma reactions

  • Ultralute technology ideal for concentrating low specific activity generated by n, gamma Mo99 production

GEN 3

  • Discussions with Mo99 manufacturers commenced in 2015

• There are over 5,000 Mo99 generators sold worldwide each week . • 50% are sold to Radiopharmacy with the remaining 50% sold directly to end users

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15

2017 Strategic Priorities and Outlook

16
Strategic Goals & Guidance Activity Timeframe
United States
FDA Approval
• Commence patient recruitment
• Complete 10th clinical site installation
• Complete Technegas particulate study
• Submit preliminary report to the USFDA
• Finalise patient recruitment
• Submit New Drug Application to the USFDA
May 2017
Q3 2017
2H 2017
2H 2017
1H 2018
1H 2018
Indication Expansion • Distribute peer reviewed publication for China COPD
• Initiate UoN-HMRI-JHH clinical trial
• Identify additional sites for pilot clinical trials targeting Technegas indication
expansion
Q2 2017
Q2 2017
2H 2017
New Product – UltraluteTM • First sales of UltraluteTM
• Finalise multi-centre multi-country trial design with the IAEA
• Complete IAEA trial
1H 2017
1H 2017
2H 2017
Expand Product &
Service Offering
• Identify and evaluate business prospects targeting growth, product extension,
diversification, improved distribution models, accretion and enhanced returns
Ongoing
Trading Update – Ongoing
Underlying Growth
(excluding China)
• FY2017 Trading YTD is in line with Board’s Expectations
• Continued growth in core underlying sales
• Modest increase in generator and PAS volumes in existing markets
• Investing in transformational growth
FY 2017
Full Year Guidance Affirmed • Excluding the positive impact of the large Chinese order FY16, the board expects
continuing modest growth in underlying Technegas volumes for FY17. Guidance
affirmed.
• Timing of orders in the pipeline could affect 1H/2H split hence guidance focused on
full year outlook
• UltraluteTM revenues, following launch in late H1 2017. Small contribution to FY17
results expected as new product builds traction. Larger contribution expected in FY18
and beyond.
FY 2017

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2017 AGM

Formal Business David Heaney

17

2017 AGM – Formal Business

Resolution Business For Against Abstain Proxy’s
Discretion
1 Remuneration report 40,875,490* 9,583 - -
2 Re-election of David Heaney 40,885,073* - - -
3 Election of Tom McDonald 40,885,073* - - -
4 Renewal of share buy-back capacity 33,229,371* 7,655,702 - -
5 Increase in the Maximum Aggregate
Annual Remuneration of Non-
Executive Directors
40,875,490* 9,583 - -

*Includes Open Useable Proxies that have instructed the Chairman to vote on their behalf and have voted in favour of the resolution.

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Cyclopharm Limited

Appendix Section

  • Cyclopharm History

  • Growth Opportunities and Key Performance Indicators

  • Technegas

  • Ultralute

  • MMI

  • Disclaimer

19

Our History

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1984 1992 2000 2001 2007 2013 Technegas European markets Vita Life Sciences USFDA Technegas Plus Ultralute[TM] discovered and established acquires program initiated generator launched technology commercialised Tetley Medical for Technegas established 1985 1995 2000 2005 2010 2015 2016 1988 1996 2003 2007 2009 2015 2016 Technegas Technegas Canadian Cyclopharm Ltd Entered molecular Maiden Dividend. USFDA Clinical enters European registered in the regulatory approval listed on the imaging market & Ultralute[TM] Trial Launched for market EU as a drug attained for ASX establishes launched Technegas Technegas MMI imaging JV

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20

Growth Opportunities and Key Performance Indicators

Technegas Technegas
USA
The USA represents the single largest market with half of the world’s nuclear medicine departments located there

Existing market for PE in the USA equates to ~480,000 patients per annum

First priority following USFDA approval is to repeat our Canadian experience by replacing the Xe133 market valued at $47m USD
Currency < 30% of revenues are $AUD related; Currently > 55 % of Technegas revenues linked to Euro.
Seasonality Historically 2H revenues are stronger due to higher procedures volume during northern hemisphere winters
Pricing & Product
Margins
In 2016 the average selling price for a per patient PAS=$50.33 AUD & Technegas Generators = $24.9k AUD.
Despite downward pressure on healthcare products globally, Technegas continues to maintain our margins.
Consolidated GM of 77.7% in 2016 made up of PAS, the profitability engine room, accounting for 75% of total Technegas revenues.
Sales Volumes PAS boxes sold in 2016= 4,284 equating to 214,200 patient studies
Underlying Technegas generators volumes continue to average 50-60 units per year in 2016 plus an additional 50 units delivered to
China end 2016
Competitive Products
Xe133 has been eliminated from the Canadian market with the introduction of Technegas.
Xe133 only used in the USA is a $USD 47M product in 2015

Kr89 – excellent imaging properties. Only available in a few countries due to limited availability and high cost

DTPA in low patient volume sites continue where Technegas is available. Used in the USA off-label

CTPA continues to dominate the PE space; however concerns with high CTPA radiation dose and improved nuclear medicine
imaging techniques are bringing referrers back to nuclear medicine VQ imaging
Intellectual Property TechnegasPlus Generator patented until 2026
A new generation of Technegas generators is under development with the goal to extend patent protection
Clinical Indications Primarily used for PE. Also used in preplanning and post surgical evaluation for lung reduction intervention
The incidence of COPD is 30x that of PE. Furthermore, COPD represents an opportunity for ongoing patient management
Distribution Cyclopharm continues to evaluate the effectiveness of Distributors/Agents/Partnerships/Independent
Facility Relocation After 20 years of tenancy, in 2016 ANSTO notified Cyclopharm that our lease would not be renewed.
One-off cost of relocation amounted to approximately $0.43M in 2016 with an ongoing increase in facility costs.

21

Growth Opportunities and Key Performance Indicators

Ultralute Ultralute
Market
Penetration
• Europe targeted as the
primary market to launch
due to the highest
concentration of end user
Mo99 generators in the
world
• 1st Generation launched in
Germany in May with initial
sales to follow 1H 2017
Margins Product launch estimates
50% GM with margin
improvement expected from
leveraging volume growth
Product
Development
• 1st Generation targeting end
users in hospitals and
clinics to be commercialised
in 2017
• 2nd Generations targeted for
Radiopharmacy will be
introduced in 2018
Other
Applications
Discussions underway with
interested parties for
extended applications with
other isotopes
MMI MMI
Revenue Volumes closely aligned with
the hospital. Continued double
digit
growth expected per annum in
the foreseeable future
Profitability EBITDA positive as of mid CY
2014
MRI
Licensing
Significant increase in
profitability
if Government funded MRI
licensing
is achieved
Expansion New outpatient facility opened
at Macquarie Centre H2 2016
Cyclopet Cyclopet
Molecular
Imaging
Following competition from
government owned enterprises,
Cyclopharm’s Board decided to
suspend commercial
operations. Subsequent to this
decision the company
successfully mediated an
outcome that resulted in
ANSTO paying $2.65M to
Cyclopharm. Cyclopharm has
no immediate intention of re-
entering this market under the
current competitive landscape.
Facility Fully written off. Discussions
underway relating to the long
term to include partnerships and
disposal of the facility

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Technegas Technology

Product Definition

Technegas is composed of Tc‐99m labelled carbon nanoparticles dispersed in high purity argon gas.

The particles are consistently well under 500 nm and due to the small, controlled particle size distribution, the dispersed radioactive particulates display pseudo‐gas characteristics permitting them to distribute and penetrate to the depth of the alveoli. Due to the lipophilic and inert nature of the radioparticulates, once deposited, the particulates remain at the site of deposition throughout the imaging procedure.

Com onents re uired for a Techne as stud : p q g y

Cyclopharm • Technegas Generator
Supplied • A single use Patient Administration Set (PAS)
• A single use patient crucible (Pulmotec)
• Sales and Service support
• Authorised Spare Parts
Nuclear Medicine • 99.9% Argon
Deparment • Ethanol
Supplied • Tc‐99m Sodium Pertechnetate sourced either from an
onsite Mo‐99 Generator or from a local Radiopharmacy

Technegas is a System

In order to deliver efficacious clinical outcomes, Technegas requires the combination of authorised:

  • Equipment and consumable sales and support

  • Regulatory representation

  • Technical provision of equipment installation and maintenance

  • Applications education in the use of the Technegas technology.

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Technegas – The Canadian Case Study

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50,000 140
Technegas Growth ‐ Canada
45,000
120
Active Generators
40,000
Patients per Annum
100
35,000
30,000
80
25,000
60
20,000
15,000
40
10,000
20
5,000
‐ 0
2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016
Generators
Patients
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  • Canada is our largest single country market with 13 consecutive years of PAS growth

  • Canada represents a strong indicator of USA acceptance

  • Xe-133 rapidly displaced by early adopters

  • Direct correlation with the number of active generators and annual consumable sales

  • Market driven by public healthcare sector

  • Market launch initiated province by province, leveraging off luminary sites

  • Market leader for diagnosing PE

  • Clinical application expansion strategy underway

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Evolution of Functional Lung Ventilation Imaging

  • Improvements in 3D imaging techniques, hybrid imaging and the advent of analytical software have dramatically improved the sensitivity and specificity in functional lung imaging with Technegas

  • Traditionally used in the diagnosis of Pulmonary Embolism, nuclear medicine functional lung ventilation imaging utilising improved imaging techniques are expanding the potential clinical utility for Technegas

  • The following Technegas images underscore the advancement in complementary technology Cyclopharm is leveraging today:

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1980s 2000 2010 2015
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SPECT with Low SPECT with Low Dose CT Dose CT & Lobular Quantification

SPECT Imaging

Planar Imaging

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Technegas – Global Indication Expansion

Targeting Chronic Obstructive Pulmonary Disease (COPD) market

Evaluating the effectiveness of Technegas in early detection of COPD and the presence of the comorbidities associated with the disease

Market Size:

  • 30x the size of total PE market

  • 65m people have moderate to severe COPD

  • Estimates show that COPD will be the third leading cause of death by 2030

Timeline:

  • Q2 2016 China trial recruitment completed

  • Q4 2016 Trial Results submitted for publication

  • Extending the COPD initiative to additional markets including in Canada, Australia and several European countries

Australian Study Specifics:

  • Patient size: 100 patients

Additional indication and applications – Asthma, Lung Reduction and CTEPH*

Technegas can provide the clinician the ability to visualise and quantify lung ventilation by region. No other diagnostic tool can provide consistent, accurate and reliable functional imaging in comparison.

Cyclopharm will leverage this market advantage in 2016 by initiating a clinical program targeting Technegas indication expansion to include:

Asthma

  • 334 million people globally

Lung Reduction Intervention

  • Application in determining ventilation pre and post lung reduction intervention

Chronic Thromboembolic Pulmonary Hypertension

  • Ventilation/Perfusion imaging is recommended

  • Up to 40 million patients globally

  • Total cost = ~$600K

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  • CTEPH = Chronic Thromboembolic Pulmonary Hypertension

Technegas Indication expansion – Targeting COPD in China

  • The Global incidence of Chronic Obstructive Pulmonary Disease (COPD) is 30x greater than that of Pulmonary Embolism (PE)

  • By 2030 COPD is estimated to be world’s 3[rd] highest cause of death

  • Between 2003 and 2033, it is predicted that China will see 65 million deaths from COPD and 18 million deaths from lung cancer

  • Following successful initial Chinese COPD trial progress, single largest Technegas order placed in June 2016 for H2 2016 delivery

Drivers of the Chinese COPD market

China Trial assessing Technegas for COPD diagnosis & management

  • Greatest producer and user of tobacco in the world*

  • Preliminary trial results suggest earlier detection than traditional Spirometry

  • Rapidly Aging Population

  • High use of biomass burning at home for cooking

  • Trial finalised in Q4 2016

  • Elevated incidence of post-pulmonary tuberculosis

  • Peer review paper submitted Q4 2016 - awaiting publication

  • Poor air quality in metropolitan areas

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China Market Potential

  • Total public hospitals 12,747

  • Private hospitals: 16,004

  • 620 Hospitals with nuclear medicine departments (~35% of tertiary hospitals)

  • 85% of Nuclear Medicine have SPECT/CT capabilities

  • 62 installed Technegas Generators in China

*Fang X et al. Chest 2011; 139: 920‐929

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Ultralute[TM]

2017 Launch - Generator Users of Mo99 Targeting Direct

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  • Ultralute[TM] v1 is targeted at the clinical end-user market

  • The European Mo99 generator market is completely Direct

  • Ultralute[TM ] registration in the EU has been determined to be a laboratory apparatus

  • The largest single market for Mo99 generators in Europe is Germany

  • Germany accounts for almost 50% of European generator market

  • Ultralute[TM] v2 is being developed for the Radiopharmacy user market

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Macquarie Medical Imaging

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  • Joint venture with:

  • 50% Alfred Health Solutions

  • 30% Macquarie University

  • 20% Cyclopharm

  • Comprehensive suite of imaging modalities

  • State of the art research platform

  • Growth and profitability linked to ramp-up of Macquarie University Hospital

  • EBIT positive since 2014

  • Sales revenue increased 8% in 2016 as outpatient initiatives implemented at Macquarie University Hospital take effect

  • Satellite Outpatient Clinic opened in 2H 2016 at nearby Macquarie Shopping Center

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CT MRI PET
Cardiac CT Ultra‐sound SPECT
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Disclaimer

Corporate Head Office

Certain views expressed here contain information derived from publicly available sources that have not been independently verified.

The presentation include certain statements, estimates and projections with respect to the anticipated future financial performance of Cyclopharm Limited and as to the markets for the company's products. Such statements, estimates and projections reflect various assumptions made by the directors concerning anticipated results, which assumptions may or may not prove to be correct. Cyclopharm Limited has not sought independent verification of information in this presentation..

While the directors believe they have reasonable grounds for each of the statements, estimates and projections and all care has been taken in the preparation, no representation or warranty, express or implied, is given as to the accuracy, completeness or correctness, likelihood of achievement or reasonableness of statements, estimates and projections contained in this presentation. Such statements, estimates and projections are by their nature subject to significant uncertainties, contingencies and assumptions.

To the maximum extent permitted by law, none of the Cyclopharm Limited, its directors, employees or agents, nor any other person accepts any liability, including, without limitation, any liability arising out of fault or negligence, for any loss arising from the use of information contained in this presentation.

All references to dollars unless otherwise specified are to Australian dollars.

Cyclopharm Limited Unit 4, 1 The Crescent Kingsgrove NSW 2208 Australia T: +61 (2) 9541 0411 F: +61 (2) 9543 0960

Enquiries

E: [email protected]

Share Registry

NextRegistries Level 16 1 Market Street Sydney NSW 2000 T: +61 (2) 9276 1700 F: +61 (2) 9251 7138

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