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Suite 1802, Level 18,
15 Castlereagh Street
Sydney NSW 2000
Australia
ABN 69 111 304 119
T: +61 2 9221 6830
F: +61 2 9221 8535
E: info@cellmid.com.au
www.cellmid.com.au
2013 Annual Report
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Contents
Chairman’s Letter
CEO’s Report
Directors’ Report
Corporate Governance Statement
Annual Financial Report
Additional Information
Corporate Directory
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Cellmid Limited (ASX:CDY)
Annual Report
ABN 69 111 304 119
Suite 1802, Level 18
15 Castlereagh Street
Sydney NSW 2000
Australia
T: +61 2 9221 6830
F: +61 2 9221 8535
E: info@cellmid.com.au
W: www.cellmid.com.au
Chairman’s
Letter
Dear Shareholder
I am pleased to present to you the 2013 Annual Report for
Cellmid Limited.
Despite the on-going challenging conditions in the equity
market in which we operate the Company has, during the year,
achieved a number of important milestones spanning the
entire spectrum of our business activities. While our progress
has not been reflected in share price performance, we believe
that our focus on building a balanced pharmaceutical product
development business with both sustainable revenues and
scale-changing upside potential will ultimately be reflected
in the share market. There are already some pleasing
indications that market sentiment to the biotechnology sector
is improving, and with the solid scientific foundations across
our three focus areas of consumer health, diagnostics, and
therapeutics, your company will be well positioned to benefit
from further improvement in these sentiments.
It is pleasing to be able to report the continuing growth and
development of our suite of diagnostic licenses based on our
core Midkine technology. The CxBladder test, developed by
our licensee Pacific Edge, was launched commercially in March
2013, providing the Company with a significant milestone
payment as well as the prospect of an early royalty stream.
Quest (Celera) have also reported good progress on their
development of a lung cancer diagnostic test using Midkine
as one of the key markers, successfully transferring the test
onto their commercial Luminex platform. We also entered
into a new license agreement with major Japanese company
Fujikura, who are already well advanced in developing a
pathology-friendly latex based assay for Midkine. We are also
confident that new research collaborations entered into during
the year will lead to more licensing opportunities in the future.
Progress with our suite of therapeutic antibodies has been
equally pleasing, with highly encouraging results
from
experiments with an animal model of diabetic nephropathy
(kidney disease). In addition, several collaborative studies are
underway on the use of Midkine antibodies in a wide range of
cancers. The results of all these studies will guide the Company
in selecting the first disease indication to take to the clinic.
We are fortunate indeed that so many researchers around the
world are now focusing on Midkine (and its antibodies) in a
wide range of disease indications; with the strong protection
of our wide-ranging Midkine patent portfolio, we will be well
placed to share in any commercial successes flowing from
this research. The fostering of this exciting research is an
important part of our development strategy, evidenced by our
sponsoring the “Excellence in Midkine Research” conference/
workshop series - next to be held in April 2014 in Kyoto,
4 Cellmid 2013 Annual Report
Japan, hosted by the scientists who discovered midkine in
the late 1980’s.
Our patent portfolio around Midkine continues to grow, with
two new granted patents during the year (Ischemia and
Vascular Occlusive Disease) to add to our existing 76 patents
and 20 patent families. Cellmid is without doubt the global
leader in Midkine intellectual property; an enviable position
indeed as its role in a wide range of disease indications is
becoming well established and recognized.
Many shareholders may not be aware that based on early
research work in Japan, Midkine has an important role in
hair growth. Although we have not yet been able to actively
pursue this application of Midkine, it did stimulate us some
time ago to seek to position the Company in this important
market sector. Thanks to the foresight and diligence of our
CEO Maria Halasz and then director (now consultant) Ko
Koike, we seized an opportunity in Japan in 2011 (?) to
acquire limited rights to a suite of scientifically validated hair
growth products based on natural plant extracts (FGF-5
inhibitors). The early response to our Australian launch of
these products has been very encouraging, so much so
that during the year we took the opportunity to acquire the
owner of the core technology, Advangen Inc. This important
acquisition, achieved with a modest cash component outlay,
provides us with access to an established Japanese market
and, importantly, the very substantial global market including
China. The Advangen acquisition gives us a real opportunity to
establish our Company as a global leader in scientifically and
clinically validated hair growth technology; part of the scale-
changing upside potential to which I referred earlier.
Further details of all these important developments can be
found in the report from our CEO and Managing Director
Maria Halasz elsewhere in this Annual Report.
During the year Robin Beaumont re-located overseas and so
resigned from the Board. We thank Robin for his sterling service
to the Company. We were delighted to welcome to the Board
Graeme Kaufman and Martin Rogers, both exceptionally well
qualified and experienced in the biotechnology sector. These
additions to the Board, together with a dedicated executive
and staff, ably led by CEO Maria Halasz, equip the Company
well to deliver on its exciting business plan. I thank all
shareholders for their continued support and encouragement.
Dr David King
Chairman
CEO’s
Report
Dear Shareholder,
I am delighted to report to you on this 2013 financial year,
which was marked by the achievement of a number of impor-
tant milestones for Cellmid in its therapeutic, diagnostic and
consumer health businesses. The financial year has seen our
Company grow substantially in its operations and revenues.
Significantly up from the previous financial year the Company’s
operational revenue reached $761,288 in 2013 ($171,273 in
2012). This growth was largely the result of increased sales
from our consumer health division.
With progress on all fronts this financial year we often received
questions about the focus of the Company. As a pharma-
ceutical product development company we are indeed fortu-
nate with programmes in all stages of the product cycle. We
have OTC (over-the-counter) and diagnostic products on the
market and novel drugs and early cancer diagnostics in devel-
opment.
We are building a company with solid revenues while maintain-
ing a strong potential for significant value inflection through
cutting edge, proprietary and highly innovative therapies and
diagnostic. We have adopted a low risk strategy to achieve
these goals and have been consistent in managing costs and
investing our shareholders’ funds wisely. We believe that this
strategy has started to pay off and 2013 has seen many major
developments.
Early response to the Australian launch of the FGF-5 inhibi-
tor hair growth products was strong, and we took advantage
of the opportunity in early 2013 to acquire the owner of the
technology, Advangen Inc., Japan. This exciting business
represented immediate access to early revenues in Japan but
most importantly shareholders should see gradual increase in
sales following the broadening of the distribution in Australia
and Japan and opening new markets in China, Europe, India
and the USA in the coming years.
The Company’s diagnostic division also started to deliver
revenue during 2013 from milestone and upfront fees. Our
third diagnostic license is also on its way with Fujikura signing
an option agreement for the exclusive use of our reagents
in Japan. Licensees Celera-Quest and Pacific Edge have
both made significant progress in their respective diagnostic
programmes. Importantly, the first commercial product with
midkine as a biomarker, CxBladder, was launched by Pacific
Edge in March 2013.
In 2013 Cellmid embarked on a programme of evaluating our
portfolio of therapeutic antibodies in multiple disease indica-
tions. Our clear objective has been to produce compelling
preclinical data that would determine a clinical development
path for this valuable asset portfolio. Strong positive results
in an animal model of diabetic nephropathy in January 2013
broadened the commercial opportunities for the Company’s
anti-midkine antibodies, while several cancer studies have
been ongoing in various locations during the year.
Our Board has gone through a transition during the finan-
cial year with the resignation of Robin Beaumont, and the
appointments of Graeme Kaufman and Martin Rogers. Robin
has guided us with his insights and we are thankful for his
contribution to the Company’s development during his tenure.
We are excited to have Graeme and Martin on board who
have already shown that their extensive industry experience is
invaluable for Cellmid.
Since the beginning of the 2013 financial year Cellmid has
raised a total of $2.6M in two separate issues of equities
or rights. In October 2012 we completed an options rights
issue and raised $545,000. In March 2013 a further $2M was
raised through a private placement of shares to sophisticated
investors.
The Company delivered a solid financial performance with
consolidated net loss down 22% to $1,541,307 ($1,972,483
in 2012), after providing for income tax, and eliminating
non-controlling equity interests. Of the total of $761,288
operating revenue over $540K was attributable to wholesale
product revenue.
Therapeutics division: Anti-midkine Antibody Programme
Cellmid’s anti-midkine antibody (MK antibody) program has
delivered compelling results during the 2013 financial year in
diabetic nephropathy. Several preclinical studies in xenograft
models of cancer have also been completed using the
Company’s proprietary antibodies during the financial year
with results due in 4Q2013.
The results of these studies will be important for making a
decision on “first in men” studies of this novel drug class. The
results have also been the culmination of 18 months of preclin-
ical studies, in which Cellmid’s proprietary MK antibodies have
been tested in several disease settings. These studies deliv-
ered valuable efficacy and mechanism of action information
in addition to showing early indication of safety. Once results
of the cancer studies are evaluated Cellmid will be ready to
undertake IND-enabling studies.
Cellmid 2013 Annual Report 5
CEO’s Report
Continued
Outstanding preclinical results – diabetic nephropathy
In March 2013 Cellmid reported on compelling results in a
diabetic nephropathy study in a mouse model of the disease
using the Company’s MK antibodies. Kidney damage was
reduced significantly, as assessed by functional and histo-
logical analysis, with kidney structure largely preserved in
the treated animals. The study provided important new infor-
mation given that it was the first time the proprietary MK
antibodies have been used in a therapeutic setting in a kidney
disease model.
Renal histological assessment showed that glomerular sclero-
sis was reduced from 48% in untreated animals to below 20%
in the MK antibody treated groups (p<0.01). Interstitial volume
was also significantly reduced, from 35% in untreated animals
to 12% in MK antibody treated groups (p<0.01). MK antibody
treatment has also maintained tubular cell height; untreated
animals had mean cell heights below 2μm, compared to 4μm
for treated animals (p<0.05).
As a further indication of the efficacy of the Company’s MK
antibodies kidney function was preserved, with treated animals
showing reduced protein leakage into the urine compared
to untreated controls. Protein casts in the kidney, indicating
damage, were also significantly reduced in antibody treated
animals (Figure 1). Importantly, the MK antibody treated
animals showed healthy weight gain and reduced mortality
compared to untreated controls; only 6.3% of treated animals
died before the end of the study, compared to 25% of the
untreated animals.
Photographs show representative histological sections from
treated and untreated mice. Protein casts are bright pink;
yellow arrows indicate large protein cast deposits.
Diabetic nephropathy is the leading cause of chronic kidney
disease globally. It is also one of the most significant long-
term complications in terms of morbidity and mortality for
patients with diabetes. In the USA alone, diabetes affects
26 million people, and the US Centre for Disease Control
(CDC) estimates that as many as one in three adults could
have diabetes by 2050 if current trends continue. Currently,
diabetic nephropathy is managed by keeping glucose levels
under control, however many of the patients develop end
stage renal disease (ESRD). It is estimated that 30-40% of all
ESRD is caused by diabetic nephropathy.
The results of the diabetic nephropathy study presented a
promising start to the Company’s review of the therapeutic
potential of its MK antibody portfolio and will form part of the
decision to select the first disease indication Cellmid can then
take into the clinic.
Preclinical studies with MK antibodies completed in
cancer – results due in 3Q2013
Several studies have been underway during the year using
the Company’s MK antibodies. These studies are expected
to deliver therapeutic information looking at tumour growth,
metastasis and angiogenesis as markers of efficacy.
Since its discovery MK’s role in cancer has been validated
extensively. Approximately 200 peer-reviewed publications
have been released on the topic. These studies, by multiple
research groups around the world, show that MK is a key
driver of tumorigenesis in at least 25 different types of cancers,
including those of the breast, lung, colorectal, gastrointestinal,
liver, pancreatic and brain. Furthermore, these studies describe
multiple mechanisms of action by which MK promotes cancer
Figure1. Anti-MK antibodies reduce protein cast deposits in the kidneys of mice with Adriamycin-induced nephropathy.
Untreated
Antibody 1
Antibody 2
6 Cellmid 2013 Annual Report
The biology of how midkine promotes cancer has been well
described by dozens of research groups globally. When devel-
oping the current preclinical studies we have postulated that
MK antibodies would have anti-cancer activities via multiple
mechanisms of action. Given that these expectations are
confirmed the MK antibody programme in cancer would be in
the lead as Cellmid’s “first in men” study.
Diagnostics division: midkine as an early cancer biomarker
It has been a productive year for our diagnostic business with
significant achievements by our licensing partners, a major
new option to license and several new collaborations. We
received around $200,000 in license fees in this business
during the 2013 year, and a subsequent $1 million in cash and
Pacific Edge shares in July 2013.
As a major step in commercialising our diagnostic assets
the Company signed an Option to License Agreement with
Fujikura in February 2013, a Japanese diagnostics company.
Fujikura is one of the largest suppliers of latex particles for
the medical diagnostics industry in Japan. While traditionally
servicing other industries with polymers and resins, Fujikura
has been actively expanding into medical diagnostics.
Under the terms of the Option to License Agreement Cellmid
was to supply Fujikura with its proprietary anti-midkine
diagnostic antibodies for validation on Fujikura’s latex platform.
Cellmid received an initial fee in February 2013. During the first
stage of the agreement Fujikura was able to reach accuracy
of 500 picogram/ml midkine in serum on its proprietary latex
diagnostic platform. This event triggered a further $400K
payment in July 2013 when Fujikura elected to exercise its
license option.
A latex based test with a 500 picogram/ml accuracy means
that the test will be able to identify individuals with elevated
midkine levels, which may lead to the development of a
number of cancer diagnostic products.
Fujikura has regulatory and product development programmes
in place to accelerate this path to market. Once Fujikura
launches its cancer diagnostic products Cellmid will also
receive royalties on any products sold. A latex based assay is
well accepted in pathology labs and it can easily be automated,
reducing processing costs.
This is a significant agreement for Cellmid not only because it
allows midkine to become a widely used test, but it is also the
first significant reagent supply agreement where the Compa-
ny’s proprietary diagnostic antibodies are sold in commercial
quantities.
Cellmid’s existing licensees, Quest and Pacific Edge, have
also achieved significant milestones in their product devel-
opment and commercialisation programmes, which resulted
in the payment of a milestone fee from Pacific Edge and an
Option fee from Fujikura, both in July 2013, after the closing
of the financial year.
Pacific Edge Limited - Bladder cancer license
Cellmid signed a license agreement with Pacific Edge Limited
in 2010 for the use of midkine as one of the biomarkers in their
bladder cancer test (Cxbladder). Pacific Edge has achieved
solid progress since the license was signed and has recently
received CLIA registration of its Pennsylvania labs. With the
CLIA registration Pacific Edge started to roll-out a sales and
marketing programme in July 2013 and they expect revenues
to grow gradually.
The license between Cellmid and Pacific Edge provides for
a milestone fee payable in shares, which is due on the first
sale of Cxbladder in the USA. Commencement of sales in July
triggered the issue of over 1M Pacific Edge shares with the
value of over $600,000 at the time. Royalties on revenues are
expected to be paid to Cellmid semi-annually.
Bladder cancer is one of the most common forms of malignan-
cies. In the United States around one million patients present
annually with haematuria; of these, 68,000 are diagnosed
with bladder cancer. Once treated patients will have regular
cystoscopies, painful urethra endoscopies,
to monitor
reoccurrence. Pacific Edge’s Cxbladder has the potential to
replace cystoscopy over time as a preferred method of patient
monitoring tool.
Cxbladder, with midkine as of the important biomarkers, has
shown outstanding performance in clinical studies to date,
with 100% sensitivity and 85% specificity in late stage bladder
cancer. This specificity is expected to increase when using it
in a monitoring setting. The test can also be used to differenti-
ate between high and low grade cancers. Cxbladder was the
subject of a comparative study of 485 patients and it signifi-
cantly outperformed other commercially available bladder
cancer tests. Importantly, it has identified 20 cases of bladder
cancer that were not identified by cystoscopy during clinical
work-up.
On the basis of sales projections released by Pacific Edge
Cellmid is expected to receive regular royalties from this
license from late 2014.
1 Clinical Laboratory Improvement Amendment, CLIA, sets standards and issues certificates for clinical laboratory testing in the United States. It is administered by
the US Centre for Medicare and Medical Devices, CMS
Cellmid 2013 Annual Report 7
CEO’s Report
Continued
Quest (Celera) Lung Cancer License
Consumer Health Division
Cellmid signed a license agreement with Quest (Celera) in
October 2009 enabling Quest to include midkine as one of
the biomarkers in a lung cancer diagnostic test. The license
covers using midkine for the early diagnosis, prognosis,
disease monitoring and management of lung cancer. The
terms of the agreement provide for a milestone payment at
the time of regulatory clearance for the lung cancer test, and
royalties to be paid semi-annually.
In March 2013 Cellmid received an annual update on the
progress made in the development of the lung cancer test. As
a significant milestone on the road to market, Quest (Celera)
has reported that they have transferred and validated their
six-marker based lung cancer test from ELISA format onto
the commercial Luminex platform. Luminex is widely used by
pathology labs internationally, and should provide the ideal
platform for product launch.
Quest has also advised that they are progressing with clinical
validation of the test. Samples obtained from the National
Cancer Institute sponsored chest X-Ray screening Prostate,
Lung, Colorectal and Ovarian Trial (PLCO) are used to
demonstrate clinical accuracy of the test. Quest (Celera) is
particularly focused on developing a test for the diagnosis of
indeterminate pulmonary nodules identified through CT scan
or chest x-ray.
Lung cancer is the leading cause of cancer death in the
United States. Currently CT scans are performed to diagnose
lung cancer; however these are expensive, lack the required
accuracy and have a poor safety profile. Cost effective, safer
and more accurate methods, such as Quest’s lung cancer
test, are urgently needed to improve survival, limit side effects
and reduce costs.
The next stage in the licensing agreement is a milestone
payment, which is due to Cellmid at the time Quest (Celera)
receives regulatory approval for the test.
Other Diagnostic Collaborations
Several research collaborations have been initiated during the
2013 financial year including a colorectal cancer screening
programme, an early diagnosis study for hepatocellular carci-
noma and two prostate cancer diagnostic projects. Cellmid
will continue to report on these as they deliver results. The
Company has also completed sample collection in its CK3000
healthy volunteer study with result expected in 4Q2013.
8 Cellmid 2013 Annual Report
During the financial year our pharmacy distribution was
expanded significantly and it was evident that our evolis®
hair growth products addressed a large and growing market
need. The Australian launch of this scientifically validated
range of products in mid-2012 resulted in early adoption by
many pharmacy buyer groups and the opening of around 700
pharmacy doors nationally. Our wholesale revenue results
exceeded internal expectations reaching just under $540,000
(for the first eight months), reflecting retail sales of over $1.2M
for the same period. This is an exceptional result for a brand
new product, in a new segment and against the minimal early
advertising spending.
Frostbland was appointed as the Company’s exclusive
Australian distributor to pharmacies in September 2012 and
has done an excellent job at getting the products on the
shelves. The roll-out of the products will be ongoing until we
reach a market penetration of around 1,000-1,200 pharma-
cies in Australia. We have commenced the systematic training
of sales and pharmacy staff amongst our current stockists. We
have regular checks on pharmacies to ensure correct stock-
ing on the products and we have commenced test advertising
in select geographical areas to learn how best we may spend
our advertising dollars.
In practice several months may pass between signing up a
pharmacy chain to sell the products and actual stocking of
shelves. Even more time is needed for the training of pharmacy
sales staff, and therefore it is not unusual to see no sales from
chain stores for 6-8 months. With this understanding, we have
a marketing plan focused on signing up independent pharma-
cies, delivering training and driving customer traffic by relevant
local advertising. An increase in sales is expected to result
nationally as both the training and advertising broadens, and
this may be accelerated once a celebrity brand ambassador
is appointed.
With the acquisition of Advangen Inc., in May 2013 the
Company’s consumer health division has become an interna-
tional business. The market for hair loss products is US$1-2
billion annually in the USA alone, affecting 52 million patients
(US Department of Health and Human Services, 2009). The
global market is estimated to be several times this amount.
There is an outstanding potential for Cellmid’s clinically proven
FGF-5 inhibitor product range to gain a share of this market.
We have also achieved a number of strategic objectives with
the acquisition. The deal enables Cellmid full ownership of
the FGF-5 inhibitor technology platform, which underpins the
Company’s existing successful évolis® hair product range
and is the basis of other Advangen Inc. brands generating
revenues in Japan. The Company has gained immediate
access to the established Japanese hair growth market. New
market opportunities will also be pursued including China
where import permits are already in place for the Lexilis® and
Jo-Ju® branded products.
The profitability of évolis® sold in Cellmid’s existing markets
has improved as there will no longer be royalties payable
to Advangen Inc. In addition, savings are expected on raw
material costs of the active ingredients. Boosting the product
pipeline of the merged group, Advangen’s FGF-5 inhibition
technology comes with a number of new candidates that
include natural extracts and novel compounds with very high
potency. An important strategic driver has been accessing the
hair growth product development expertise which comes with
the scientific and regulatory staff of Advangen Inc. This should
greatly facilitate Cellmid’s own programme to develop midkine
as a hair loss treatment.
This is a company changing deal for Cellmid. Our objective is
to establish ourselves as a global leader in scientifically and
clinically validated hair growth technology building a substan-
tial business, which provides cash flow and adds significant
shareholder value.
Patent Portfolio Update
Managing our patent portfolio has been one of the top priori-
ties this year as we have faced several challenging prosecu-
tions. As always we have had a very strong focus on build-
ing a cohesive strategy that makes commercial sense while
retaining our position as the midkine company. Our portfolio
currently stands at 78 patents and 20 patent families, with
two new granted patents in the 2013 financial year, as Cellmid
remains the global leader in MK intellectual property.
In July 2012 the Company was granted a key midkine protein
patent by the United States Patent and Trademark Office
(USPTO) entitled “Nitric oxide synthase activator” (‘277).
This is a fundamentally important patent in the Company’s
programme for the treatment of various forms of ischemia
including heart attack. Patent ‘277 protects the use of midkine
to treat ischemic disorders including heart attack. Specifically,
this patent covers the stimulation of nitric oxide (NO) synthesis
by MK injection. Nitric oxide is a key signalling molecule that
mediates blood flow, vasodilation and angiogenesis (growth of
new blood vessels).
While this programme has not been advanced significantly
during the 2013 financial year due to resourcing issues, it
remains one of the most valuable assets with potential for
early partnering.
In January 2013 the European Patent Office (EPO) granted
Cellmid’s patent application 06746805.8 entitled “Pharma-
ceutical composition for vascular occlusive disease”. The
application was filed in May 2006 and the patent is expected
to expire in 2026. The claims granted cover the use of short
interfering RNAs (siRNAs) to prevent midkine expression in
blood vessel walls. Animal studies show that midkine expres-
sion in damaged blood vessels contributes significantly to
vessel narrowing and obstruction, and inhibiting midkine
prevents or reduces this narrowing.
Vascular occlusive disease is the biggest cause of prema-
ture death in Western nations. Vascular occlusive disease
occurs where blood vessels are narrowed or blocked, and
it is observed at many sites in the body, including the heart
(coronary heart disease, CHD), the brain (stroke), the kidney
(renovascular disease) and the limbs (peripheral vascular
disease such as deep vein thrombosis).
Targeting MK in vascular disease is a novel potential treatment
of both the initial vessel narrowing (stenosis) and the re-occur-
rence of narrowing (restenosis) that frequently occurs after
surgical interventions such as stenting. Cellmid does not have
an siRNA programme in this indication, however this patent
could represent product pipeline and partnering opportunities
in the future. With this patent Cellmid’s patent coverage for
siRNA and antibodies extends across cardiovascular disease,
inflammatory and autoimmune diseases, cancer, multiple
sclerosis and surgical adhesion.
Although we can look back to an exceptionally productive
financial year, it is not entirely satisfying as the Company’s
share price hasn’t tracked the significant increase in the value
of our assets. However, we believe that continuing on our
growth path and taking advantage of the improving sentiment
towards our sector may ultimately change this.
I would like to thank our Chairman, Dr David King, the Board
and the committed Cellmid team for their contribution in
achieving these substantial milestones this financial year. I
would also like to thank all our shareholders for their active
support.
Maria Halasz
CEO and Managing Director
Cellmid 2013 Annual Report 9
Directors’
Report
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Contents
Directors’ Report
Auditor’s Independence Declaration
Corporate Governance Statement
Annual Financial Report
Your directors present their report, together with the financial statements of the Group, being Cellmid Limited (Cellmid or
the Company) and its controlled entities (Group), for the financial year ended 30 June 2013.
Directors
The following persons were directors of Cellmid during the financial year and up to the date of this report, unless otherwise
stated:
Dr David King (appointed 18 January 2008)
Ms Maria Halasz (appointed 19 November 2007)
Mr Robin Beaumont (resigned 27 August 2012)
Mr Graeme Kaufman (appointed 27 August 2012)
Mr Martin Rogers (appointed 19 September 2012)
Other Key Management Personnel
The following persons were key management personnel of Cellmid during the financial year and up to the date of this
report, unless otherwise stated:
Mr Nicholas Falzon (Company Secretary appointed 6 October 2010)
Ms Jillian McGregor (Company Secretary appointed 16 July 2013)
Mr Andrew Bald (Company Secretary appointed 6 August 2012 and resigned 8 April 2013)
Principal Activities and Significant Changes in the Nature of Activities
The principal activities of the Group during the financial year were:
• the development and commercialisation of diagnostic and therapeutic products for the management of diseases such
as cancer and various chronic inflammatory conditions by targeting midkine (Midkine Business); and
• the development and sale of over-the-counter (OTC) treatments to alleviate excessive and abnormal hair loss and re-
establish the natural hair growth cycle (Consumer Health Business)
There were no significant changes in the nature of the activities during the financial year.
Operating Results and Review of Operations for the Year
The consolidated net loss of the Group was down 22% to $1,541,307 ($1,972,483 in 2012), after providing for income
tax, and eliminating non-controlling equity interests. Revenue from product sales was up by more than 300% to $541,649
($132,826 in 2012), while total Revenue was up by 345% to $761,288 for the year ($171,273 in 2012).
Cellmid 2013 Annual Report 11
Directors’ Report
Continued
REVIEW OF OPERATIONS
The Group has grown its Consumer Health Business significantly during the reporting period and, with the acquisition of
Advangen Inc., opened up a global opportunity for the commercialisation of its FGF-5 inhibitor hair growth products.
The Midkine Business has reached critical product development objectives in relation to the midkine antibody program and
commencing the studies necessary for the ‘first in man’ phase 1/2a clinical trials of its anti-midkine antibodies in multiple
solid tumours. Significant progress has also been achieved in the Group’s diagnostic business with the launch of the first
commercial product with midkine as a biomarker, CxBladder by Pacific Edge Limited, and a new option to license agree-
ment with Fujikura Kasei (Japan).
Consumer Health Business - Acquisition of Advangen Inc. means a global opportunity for the FGF-5 inhibitor hair
growth products
Advangen International Pty Ltd, a controlled entity, was set up to commercialise over-the-counter hair growth products
based on the FGF-5 inhibition technology developed by Advangen Inc. (Japan). Advangen International Pty Ltd originally
negotiated exclusive manufacturing and distribution rights for Australia, USA and Europe and commenced its commercial
proof of concept program in September 2012 in Australia by the appointment of a pharmacy distributor.
The results of the commercial proof of concept program have indicated strong global potential for the FGF-5 inhibitor hair
growth products. To fully exploit this opportunity the Group acquired Advangen Inc. (Japan) in May 2013. The transaction
involved the payment of $1.2 million in cash and the issuing of 55,737,624 Cellmid shares at an agreed price of $0.05 each
with a total deal value of $4.0 million. At the time of the acquisition Advangen Inc. had unaudited annualised sales of around
$1 million and cash and equivalents of around $400,000.
The acquisition of Advangen Inc. is expected to make a significant positive impact on the Group’s operations in future
financial years. It provides global ownership of the FGF-5 inhibition technology and immediate access to the established
Japanese markets for the products. It is a whole-of-chain acquisition resulting in reduced cost of goods and no royalties.
The acquisition delivered valuable additional assets including Chinese import permits for the Lexilis and Jo-Ju brands, with
the potential to accelerate geographical expansion of the distribution. It also provides opportunities for product improve-
ments and further clinical validation programs to expand the markets for chemotherapy related hair loss and androgenic
alopecia.
Midkine business
Advances in therapeutic product development - midkine antibodies heading to the clinic
Under this program the Group has been developing its anti-midkine antibody drugs for the treatment of cancer and inflam-
matory diseases. The program received a significant boost during the period with positive results in its pre-clinical programs
in diabetic nephropathy and solid tumours, paving the way for clinical development.
In January 2013 the Group received results indicating that its antibody drug reduced mortality and preserved kidney
function in a study of a mouse model of diabetic nephropathy. Kidney damage was significantly reduced in this Adriamycin
induced kidney damage model. This bolstered the Group’s preclinical data package, which has already included positive
efficacy results in animal models of several cancer types such as osteosarcoma, rectal carcinoma and glioblastoma. The
review of the pharmacological data package resulted in the development of a clinical development plan involving a phase
1/2a study for the Group’s anti-midkine antibody drug in multiple solid tumour types. The program is expected to be imple-
mented in the coming financial year.
Midkine (MK) Diagnostic Program
Two of the Group’s licensees, Pacific Edge Limited and Celera-Quest, made significant progress towards commercialisa-
tion of their respective products. The Group has also signed an option to license agreement with Fujikura Kasei for the use
of two proprietary anti-midkine antibodies in Fujikura’s latex diagnostic products. Internal diagnostic programs, including
12 Cellmid 2013 Annual Report
the colorectal cancer project at the John Hunter Hospital are progressing with sample collection and testing. This is a
prospective program with results expected in late 2014.
Pacific Edge Limited - launched CxBladder in the USA with midkine as one of the biomarkers
The Group signed a license agreement with Pacific Edge Limited in 2010 for the use of the Group’s biomarker, midkine, as
one of the biomarkers in CxBladder, a bladder cancer diagnostic test. According to the terms of the license Pacific Edge
paid an upfront fee and was to pay a milestone fee in shares on reaching first sale of the product outside of Australia and
New Zealand. Pacific Edge has made solid progress towards this milestone during the reporting period and successfully
launched its CxBladder test in the USA in March 2013. Pacific Edge reported setting up a sales force to urologists in April
with sales expected to commence shortly.
Celera-Quest license update
The Group signed a license agreement with Celera-Quest in 2009 enabling Quest to use midkine as one of six biomarkers
in their test for the early diagnosis, prognosis and disease management of lung cancer. The Group received an upfront
payment at the time of signing, a milestone payment will become payable by Celera-Quest at the time of regulatory
clearance and royalties on sales. Celera-Quest provided their annual update to the Group in March 2013 confirming that
they have transferred and validated the six marker assay on the Luminex platform. They have also advised that they are
progressing with further clinical validation using serum samples from a National Cancer Institute sponsored trial.
Fujikura Kasei option to license
The Group signed an Option to License Agreement with Fujikura Kasei for the exclusive supply of the Group’s proprietary
antibodies for validation in Fujikura’s latex diagnostic platform. The agreement provides that Fujikura will proceed to license
subject to reaching the minimum 500 picogram/mL limit of detection. This is to ensure that Fujikura’s latex assay will be
able to identify individuals with elevated midkine levels. The validation program was progressing well during the reporting
period. Fujikura paid an option fee on signing and will pay a milestone fee upon completion of the validation and exercise
of its option to license.
Intellectual Property update
The Group has a large and valuable patent portfolio which consists of 78 patents across 20 patent families. Of these 52
patents have been granted, 25 filed or under examination and one in PCT stage.
Two significant midkine therapeutic patents have been granted during the reporting period. The patent entitled “Pharma-
ceutical composition for vascular occlusive disease” (06746805.6) was granted by the European Patent office in January
2013. The Group’s patent application “Nitric oxide Synthase activator” (12/593,277) was granted in the USA in July 2012.
Financial Position
The net assets of the Group, after eliminating non-controlling interests, are significantly up at $5,305,157 ($2,089,484 as at
30 June 2012). The directors believe that the Group is in a stable financial position to expand and grow its current operations.
Significant Changes in the State of Affairs
The Group acquired Advangen Inc. (Japan) in May 2013. The transaction involved the payment of $1.2 million in cash and
the issuing of 55,737,624 Cellmid shares at an agreed price of $0.05 each with a total deal value of $4 million. In the finan-
cial statement the transaction is recorded at $2.9 million (“fair value”) as Cellmid shares were traded on market at $0.03
at the time of the acquisition. The acquisition is expected to have a significant positive impact on the Group’s operations.
Dividends Paid or Recommended
The Company has not paid or declared any dividends during the financial year (2012: nil).
Cellmid 2013 Annual Report 13
Directors’ Report
Continued
Events after the Reporting Period
There are two items which have occured after the reporting date as follows:
- Pacific Edge have issued 1,084,622 shares to Cellmid having achieved their requisite milestone. The shares have been
issued pursuant to the midkine diagnostic licence agreement signed on 17 May 2010; and
- The escrow shares issued during the year will be released within the next 12 months.
Other than these items, no other matter or circumstance has arisen since 30 June 2013 that has significantly affected,
or may significantly affect the Group’s operations, the results of those operations, or the Group’s state of affairs in future
financial years.
Future Developments, Prospects and Business Strategies
Likely developments, future prospects and business strategies of the operations of the Group and the expected results of
those operations have not been included in this report as the directors believe, on reasonable grounds, that the inclusion
of such information could result in unreasonable prejudice to the consolidated Group.
Environmental Issues
The Group’s operations are not subject to significant environmental regulations under the laws of the Commonwealth and
the state.
Board and Audit Committee meetings
The number of meetings of directors held during the year and the number of meetings attended by each director were as
follows:
Ms Maria Halasz
Dr David King
Mr Robin Beaumont
Mr Graeme Kaufman
Mr Martin Rogers
Board meetings
Audit Committee meetings
Number
eligible to
attend
Number
attended
Number
eligible to
attend
Number
attended
6
6
3
3
3
6
6
3
3
3
5*
5
3
2
2
5
5
3
2
2
The Nomination Committee and Remuneration Committee of the board of directors (Board) met on several occasions
during the financial year on an informal basis.
* Maria Halasz was in attendance at audit committee and remuneration committee meetings by invitation.
14 Cellmid 2013 Annual Report
Information on Directors and Company Secretaries
David King
Qualifications
– Chairman (Non-executive)
– Fellow of The Australian Institute of Company Directors, Fellow of the
Australian Institute of Geoscientists and a PHD in Seismology from the
Australian National University.
Experience
– Experience in high growth companies and a track record in starting
business ventures and developing them into attractive investment and/
or take-over targets.
Interest in Shares and Options
– Shares: 22,500,000 indirectly held.
Options: 11,250,000 indirectly held (Expiry: 23 October 2016, exercis-
able at $0.034 each).
Special Responsibilities
– Chairman of the Remuneration Committee and Nomination Committee.
Directorships held in other listed
entities during the three years prior to
the current year
– Current directorships - Robust Resources Limited, Republic Gold
Limited
Previous directorship - Gas2Grid Limited and Ausmon Resources
Limited and Sapex Limited, Eastern Star Gas Limited.
Maria Halasz
Qualifications
Experience
– Managing Director (Executive)
– A Graduate of the Australian Institute of Company Directors; MBA, BSc
in microbiology.
– Over 19 years experience in biotechnology companies; initially working
in executive positions in biotechnology firms, then managing investment
funds and later holding senior positions in corporate finance specialising
in life sciences.
Interest in Shares and Options
– Shares: 1,050,000 directly held.
Shares: 5,700,000 indirectly held.
Options: 7,000,000 (Expiry: 20 November 2014, exercisable at $0.056
each) indirectly held.
Options: 1,362,625 (Expiry: 23 October 2016, exercisable at $0.034
each) indirectly held.
Options: 5,000,000 (Expiry: 15 June 2017, exercisable at $0.032 each)
indirectly held.
(Shares in Advangen International Pty Ltd: 278,049, indirectly held).
Special Responsibilities
– Managing Director and Chief Executive Officer.
Directorships held in other listed
entities during the three years prior to
the current year
– None
Cellmid 2013 Annual Report 15
Directors’ Report
Continued
Graeme Kaufman
– Director – Non-executive (Appointed 27th August 2012)
Qualifications
Experience
– BSc & MBA from Melbourne University
– Over 45 years’ experience in biotechnology spanning technical,
commercial and financial areas. Having worked for 34 years at CSL
Limited, Australia’s largest biopharmaceutical company, he held senior
positions including Production Director, General Manager Finance and
General Manager Biosciences.
Interest in Shares and Options
– Options: 1,000,000 (Expiry: 1 June 2014, exercisable at $0.05 each)
directly held.
Special Responsibilities
– Chairman of the Audit Committee and member of the Remuneration
Directorships held in other listed
entities during the three years prior to
the current year
and Nomination Committee.
– Bionomics Ltd and IDT Australia Ltd
Martin Rogers
Qualifications
Experience
– Director – Non-executive (Appointed 19th September 2012)
– Chemical Engineering and Science Degrees from University of New
South Wales
– Martin Rogers is the former CEO and current non-executive director
of Prima BioMed Ltd. He has a depth of experience in incubating
companies and publicly listed organisations. Mr Rogers has experience
in all aspects of financial, strategic and operational management and
has raised over $100m in equity.
Interest in Shares and Options
– Shares: 5,155,700 shares indirectly held.
Options: 44,000,000 (Expiry: 23 October 2016, exercisable at $0.034
each) indirectly held
Special Responsibilities
– Member of the Audit Committee and member of the Remuneration
Directorships held in other listed
entities during the three years prior to
the current year
Jillian McGregor
Qualifications
Experience
Committee
– Consegna Limited, Prima BioMed Ltd and OncoSil Medical Limited
– Company Secretary (Appointed 16 July 2013)
– Bachelor of commerce and law from University of New South Wales
– Jillian has worked as a corporate lawyer for more than 15 years in mid
and top tier Australian law firms. During this time she has provided
Corporations Act and ASX Listing Rule advice to many ASX listed
companies including advice on related party transactions, capital raising
requirements, and meeting continuous disclosure requirements.
Interest in Shares and Options
Special Responsibilities
Directorships held in other listed
entities during the three years prior to
the current year
– Nil
– Nil
– Nil
16 Cellmid 2013 Annual Report
Nicholas Falzon
Qualifications
Experience
– Company Secretary & Financial Controller
– Bachelor of Business at UTS and a member of the Institute of
Chartered Accountants of Australia
– As a partner at Lawler Partners Nicholas works with a number of listed
and unlisted companies advising them on all aspects of their financial
management.
Interest in Shares and Options
Special Responsibilities
Directorships held in other listed
entities during the three years prior to
the current year
– Nil
– Nil
– Nil
Remuneration report
The information provided in this remuneration report has been audited as required by section 308 (3C) of the Corporations
Act 2001.
The remuneration report is set out under the following main headings:
A. Principles used to determine the nature and amount of remuneration
B. Details of remuneration
C. Service agreements
D. Share-based compensation
E. Additional information
A. Principles used to determine the nature and amount of remuneration
The performance of the Group depends on the quality of its directors and executives.
To prosper, the Group must attract, motivate and retain highly skilled directors and executives. To this end, the Group
embodies the following principles in its remuneration framework:
• provide competitive rewards to attract high calibre executives; and
• establish appropriate performance hurdles in relation to variable executive remuneration.
The Board assesses the appropriateness of the nature and amount of remuneration of directors and senior managers of
the Group on a periodic basis by reference to relevant employment market conditions with the overall objective of ensuring
maximum stakeholder benefit from the retention of a high quality Board and executive team.
Remuneration structure
In accordance with best practice corporate governance, the structure of non-executive director and senior manager
remuneration is separate and distinct.
Cellmid 2013 Annual Report 17
Directors’ Report
Continued
Non-executive director remuneration
Objective
The Board seeks to set aggregate remuneration at a level that provides the Group with the ability to attract and retain direc-
tors of the highest calibre, while incurring costs that are acceptable to shareholders.
Structure
Each non-executive director receives a fixed fee for being a director of the Group.
The constitution and the ASX Listing Rules specify that the maximum aggregate remuneration of non-executive directors
shall be determined from time to time by a general meeting of shareholders. At the general meeting of shareholders in
2005, the maximum amount was set at $300,000 per annum. In 2013, the Group paid non-executive directors a total of
$145,802 (2012: $143,349).
The amount of aggregate remuneration sought to be approved by shareholders and the fixed fees paid to directors are
reviewed annually. The Board considers fees paid to non-executive directors of comparable companies when undertaking
the annual review process.
Executive remuneration
Objective
The Group aims to reward executives with a level and mix of remuneration commensurate with their position and respon-
sibilities within the Group and so as to:
•
reward executives for Group and individual performance against targets set by reference to appropriate benchmarks;
• align the interests of executives with those of shareholders; and
• ensure total remuneration is competitive by market standards.
Structure
A policy of the Board is the establishment of employment or consulting contracts with the CEO and other senior executives.
Remuneration consists of fixed remuneration under an employment or consultancy agreement and may include long
term equity-based incentives that are subject to satisfaction of performance conditions. The equity-based incentives are
intended to retain key executives and reward performance against agreed performance objectives.
Fixed remuneration
The level of fixed remuneration is set so as to provide a base level of remuneration that is both appropriate to the position
and competitive in the market.
Fixed remuneration is reviewed annually by the Board and the process consists of a review of Group-wide and individual
performance, relevant comparative remuneration in the market, and internal and (where appropriate) external advice on
policies and practices.
Senior managers are given the opportunity to receive their fixed (primary) remuneration in a variety of forms including
cash and expense payment plans, such that the manner of payment chosen is optimal for the recipient without creating
additional cost for the Group.
18 Cellmid 2013 Annual Report
Remuneration policy and performance
Other than the CEO, Ms Halasz, none of the director’s remuneration is’at risk’ remuneration. Refer to the table below for
further information on Ms Halasz’s remuneration.
B. Details of remuneration (audited)
Details of the remuneration of the directors and key management personnel of the group (as defined in AASB 124 Related
Party Disclosures) and the highest paid executives of Cellmid are set out in the following tables.
2013
Name
Short-term benefits
Post employment
benefits
Share-
based
payment
Cash salary and
Cash bonus
Non-monetary
Superannuation
Retirement
Options
Total
Non-executive directors
David King (Chairman)
Robin Beaumont 2
Graeme Kaufman
Martin Rogers
Total non-executive
directors
fees
$
65,000
4,767
34,058
33,062
136,887
Executive directors and key Management
Maria Halasz
Nicholas Falzon 1
Total Executive directors
and key Management
Total
400,000
-
400,000
536,887
$
-
-
-
-
-
-
-
-
-
benefits
$
-
-
-
-
-
-
-
-
-
$
5,850
-
3,065
-
8,915
36,000
-
36,000
44,915
benefits
$
-
-
-
-
-
-
-
-
-
$
-
-
-
-
-
-
-
-
-
$
70,850
4,767
37,123
33,062
145,802
436,000
-
436,000
581,802
1. Nicholas Falzon, company secretary, was appointed on 6 October 2010, is a partner of Lawler Partners Pty Ltd
who provides accounting and company secretarial services to Cellmid Limited. The contract is based on normal
commercial terms. A total of $92,125 (2012 $75,250) was received by Lawler Partners Pty Limited in relation to this
contract for the year.
2. Robin Beaumont resigned as director on 27th August 2012.
Cellmid 2013 Annual Report 19
Directors’ Report
Continued
2012
Name
Short-term benefits
Post employment
Benefits
Share-
based
payment
Cash salary and
Cash bonus
Non-monetary
Superannuation
Retirement
Options
Total
fees
benefits
benefits
Non-executive directors
David King (Chairman)
Robin Beaumont
Total non-executive
directors
65,000
30,000
95,000
Executive directors and key Management
Maria Halasz
Nicholas Falzon 1
Total Executive directors
and key Management
Total
400,000
-
400,000
495,000
-
-
-
-
-
-
-
-
-
-
-
-
-
-
5,850
-
5,850
36,000
-
36,000
41,850
-
-
-
-
-
-
-
-
42,499
42,499
70,850
72,499
143,349
30,500
466,500
-
-
-
-
466,500
609,849
1. Nicholas Falzon, company secretary, was appointed on 6 October 2010, is the partner of Lawler Partners Pty Ltd
who provides accounting and company secretarial services to Cellmid Limited. The contract is based on normal
commercial terms. A total of $75,250 (2011 $52,300) was received by Lawler Partners Pty Limited in relation to this
contract for the year.
The relative proportions of remuneration that are linked to performance and those that are fixed are as follows:
Name
Fixed remuneration
At risk STI
At risk LTI
2013
2012
2013
2012
2013
2012
Directors
David King
Maria Halasz
Robin Beaumont
Graeme Kaufman
Martin Rogers
100%
100%
100%
100%
100%
100%
96%
41%
n/a
n/a
Other company and group executives
Nicholas Falzon
Andrew Bursill
100%
100%
100%
n/a
-
-
-
-
-
-
-
-
-
-
-
-
-
n/a
-
-
-
-
-
-
-
-
4%
59%
n/a
n/a
-
-
20 Cellmid 2013 Annual Report
C. Service agreements
The CEO, Maria Halasz, is an employee of the group under an agreement signed on 21 September 2007. Under the terms
of the present contract:
• Ms Halasz may resign from her position and thus terminate this contract by giving six months’ written notice. On
resignation any unvested options will be forfeited.
• The group may terminate the employment agreement by providing six months’ written notice or providing payment in
lieu of the notice period (based on the fixed component of Ms Halasz’s remuneration).
• The group may terminate the contract at any time without notice if serious misconduct has occurred. Where termination
with cause occurs, the CEO is only entitled to that portion of remuneration which is fixed, and only up to the date of
termination. On termination with cause, any unvested options will immediately be forfeited.
• Ms Halasz’s employment agreement provides for issuing performance incentives subject to the discretion of the board.
During the 2013 financial year there has been no performance incentive issued to Ms Halasz.
D. Share-based compensation
Options
2013
Options Granted
in 2013
Value of options
at grant date
Options Vested
In 2013
Value of options
expensed in
2013
Proportion of
Remuneration
$
-
-
-
-
-
-
%
0%
0%
0%
0%
0%
0%
Maria Halasz
David King
Graeme Kaufman
Martin Rogers
Robin Beaumont
Total
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
No options were granted to the directors as share-based compensation during the financial year.
No options have been granted since the end of the financial year.
This concludes the remuneration report which has been audited.
Loan to directors and executives
There were no loans to directors or executives during or since the end of the year.
Cellmid 2013 Annual Report 21
Directors’ Report
Continued
Shares under option
Unissued ordinary shares of Cellmid under option at the date of this report are as follows:
Unlisted options
Unlisted options
Unlisted options
Unlisted options
Unlisted options
Unlisted options
Unlisted options
Unlisted options
Listed options
Unlisted options
Unlisted options
Total
Expiry Date
19 March 2014
01 June 2014
01 July 2014
20 November 2014
20 November 2014
19 February 2015
15 November 2015
15 November 2016
23 October 2016
15 June 2017
14 August 2017
Exercise Price
Number under option
$0.05
$0.05
$0.05
$0.056
$0.035
$0.062
$0.10
$0.03
$0.034
$0.032
$0.034
27,198,435
8,250,000
5,002,006
7,000,000
2,000,000
600,000
100,000
3,971,962
290,542,770
5,000,000
1,440,000
351,105,173
No shares were issued on the exercise of options during the income year ended 30 June 2013 (2012: nil).
No amounts are unpaid on any of the shares for the 2013 income year (2012:$nil).
2,000,000 options were lapsed during the income year ended 30 June 2013 (2012: 6,599,995).
Director and Officer Insurance
During the financial year, the Group paid a premium to insure the directors and officers of the Group.
The liabilities insured are legal costs that may be incurred in defending civil or criminal proceedings that may be brought
against the officers in their capacity as officers of the Group, and any other payments arising from liabilities incurred by the
officers in connection with such proceedings. This does not include such liabilities (other than legal costs) that arise from
conduct involving a wilful breach of duty by the officers or the improper use by the officers of their position or of informa-
tion to gain advantage for them or someone else or to cause detriment to the Company. It is not possible to apportion the
premium between amounts relating to the insurance against legal costs and those relating to other liabilities.
Indemnifying Officers or Auditor
During or since the end of the financial year, the Group has given an indemnity or entered into an agreement to indemnify,
or paid or agreed to pay insurance premiums in favour of its directors as follows:
• a right to access certain Board papers of the Group during the period of their tenure and for a period of seven years
after that tenure ends
• subject to the Corporation Act 2001, an indemnity in respect of liability to persons other the Company and its related
bodies corporate that they may incur while acting in their capacity as an officer of the Company or a related body
corporate, except for specified liabilities where that liability involves a lack of good faith or is for legal costs for defending
certain legal proceedings; and
•
the requirement that the Group maintain appropriate directors’ and officers’ insurance for the officer.
No liability has arisen under these indemnities as at the date of the report.
There is no indemnity cover in favour of the auditor of the Group during the financial year.
22 Cellmid 2013 Annual Report
Proceedings on behalf of the Company
No person has applied to the Court under section 237 of the Corporations Act 2001 for leave to bring proceedings on
behalf of the Group, or to intervene in any proceedings to which the Group is a party, for the purpose of taking responsibility
on behalf of the Group for all or part of those proceedings.
No proceedings have been brought or intervened in on behalf of the Group with leave of the Court under section 237 of
the Corporations Act 2001.
Non-audit services
The Group may decide to employ the auditor on assignments additional to their statutory audit duties where the auditor’s
expertise and experience with the Group and/or the Group are important.
Details of the amounts paid or payable to the auditor, BDO (formerly PKF) for audit and non-audit services provided during
the year are set out below.
Auditing or reviewing the financial statement
BDO (formerly PKF)
BDO Japan
Rounding off of amounts
Consolidated group
2013
$
54,900
10,200
65,100
2012
$
45,000
-
45,000
The Company is of the kind referred to in ASIC Class Order 98/0100, dated 10 July 1998, and in accordance with that
Class Order amounts in the directors’ report and the annual financial report are rounded off to a dollar, unless otherwise
indicated.
Auditor’s Declaration
The lead auditor’s independence declaration under s 307C of the Corporations Act 2001 is set out on page 24 for the
annual report ended 30 June 2013.
This report is signed in accordance with a resolution of the Board of Directors made pursuant to s.298(2) of the Corpora-
tions Act 2001.
On behalf of the directors
Director
Dr David King
Sydney
Dated this day of 28 August 2013
Cellmid 2013 Annual Report 23
24 Cellmid 2013 Annual Report
Corporate
Governance Statement
Unless disclosed below, all the recommendations of the ASX Corporate Governance Council (including 2010 amendments)
have been applied for the entire financial year ended 30 June 2013 (ASX Principles).
Board Composition
The skills, experience and expertise relevant to the position of each director who is in office at the date of the annual report
and their term of office are detailed in the directors’ report.
The names of independent directors that have served on the board of directors of the Company (Board) during the period are:
o David King
o Robin Beaumont (Resigned on 27 August 2012)
o Graeme Kaufman (Appointed on 27 August 2012)
o Martin Rogers (Appointed on 19 September 2012)
Independent directors are those who have the ability to exercise their duties unfettered by any business or other relationship
and are willing to express their opinions free of concern about their position or the position of any third party. The Board
does not believe it is possible to draft a list of criteria which is appropriate to characterise, in all circumstances, whether a
non-executive director is independent. However, in determining the independent status of a director the Board will consider
whether the director:
o
is a substantial shareholder of the Company or an officer of, or otherwise associated directly with, a substantial
shareholder of the Company;
o
is employed, or has previously been employed in an executive capacity by the Company or another group member;
o has within the last three years been a principal of a material professional adviser or a material consultant to the Company
or another group member, or an employee materially associated with the service provided;
o
is a material supplier or customer of the company or another group member, or an officer of or otherwise associated
directly or indirectly with a material supplier or customer;
o has a material contractual relationship with the Company or another group member other than as a director.
In some cases the Board needs to make an assessment of the materiality of a relationship in order to determine if a direc-
tor is independent. A “material relationship” includes a direct or indirect interest or relationship that could reasonably be
considered to influence in a material way the director’s decisions in relation to the Company. When considering whether a
relationship is “material”, the Board will consider the materiality to each of the Company, the director and the person or or-
ganisation with which the director is related (as customer, supplier, or adviser). The Board has not set materiality thresholds,
considering it more effective to assess relationships on the individual circumstances applicable on a case-by-case basis
and where appropriate, with the assistance of external advice.
Independent directors have the right to seek independent professional advice in the furtherance of their duties as directors
at the Company’s expense. Written approval must be obtained from the Chairman prior to incurring any expense on behalf
of the Company.
David King, Graeme Kaufman and Martin Rogers are members of the nomination committee. These members have attend-
ed meetings of the nomination committee on an ad hoc basis as needed during the year. When appointing new directors,
the Board and the nomination committee look to ensure that an appropriate balance of skills, experience, expertise and
diversity is maintained. The Board has not approved a formal nomination committee charter and as such, no such charter
or summary of such charter is disclosed on the company’s website.
Cellmid 2013 Annual Report 25
Corporate Governance
Continued
Ethical Standards
The Board acknowledges and emphasises the importance of all directors and employees maintaining the highest stand-
ards of corporate governance practice and ethical conduct.
A code of conduct has been established requiring directors and employees to:
• act honestly and in good faith;
• exercise due care and diligence in fulfilling the functions of office;
• avoid conflicts and make full disclosure of any possible conflict of interest;
• comply with the law;
• encourage the reporting and investigating of unlawful and unethical behaviour; and
• comply with the share trading policy outlined in the code of conduct.
Directors are obliged to be independent in judgment and ensure all reasonable steps are taken to ensure due care is taken
by the Board in making sound decisions.
Diversity Policy
Diversity includes, but is not limited to, gender, age, ethnicity and cultural background. The Company is committed to
diversity and recognises the benefits arising from employee and Board diversity and the importance of benefiting from all
available talent.
The Board believes that the Company benefits from this diversity.
However, due to the size of the Company and small number of persons employed by the company and its controlled enti-
ties, the Board has not established a formal diversity policy in accordance with Recommendation 3.2 of the ASX Principles.
As such and for the same reasons, the Company is not able to disclose in this annual report the measurable objectives for
achieving gender diversity in accordance with the diversity policy and progress towards achieving those objectives.
The Company is able to disclose the following gender diversity statistics for the company and its controlled entities as at
the date of this annual report:
• women employees (67%);
• women in senior executive positions (57%); and
• women on the Board (25%).
Trading Policy
The Company has a policy on the sale and purchase of its securities by its directors and employees. In addition, this policy
applies to advisers, contractors and consultants who may obtain confidential or price sensitive information in relation to
the Company.
The purpose of the policy is to avoid conduct known as ‘insider trading’. In some respects, the Company’s policy extends
beyond the strict requirements of the Corporations Act 2001 (Cth) (Corporations Act).
Audit Committee
The names and qualifications of those appointed to the audit committee and their attendance at meetings of the committee
are included in the directors’ report.
26 Cellmid 2013 Annual Report
CEO/CFO Declaration
As required by section 295A of the Corporations Act, the CEO and CFO have declared that in their opinion:
a. the financial records of the company and controlled entities for the financial year have been properly maintained in
accordance with section 286 of the Corporations Act;
b. the financial statements and notes for the financial year comply with accounting standards;
c. the financial statements and notes for the financial year give a true and fair view of the financial position and performance
of the company and its controlled entities in accordance section 297 of the Corporations Act;
d. any other matters prescribed by the Corporations Regulations in relation to the financial statements and notes for the
financial year have been satisfied.
In addition, in accordance with Recommendation 7.3 of the ASX Principles, the CEO and CFO stated to the Board that
the declaration provided under section 295A of the Corporations Act is founded on a sound system of risk management
and internal control and that the system is operating effectively in all material respects in relation to financial reporting risks.
Performance Evaluation
An annual performance evaluation of the Board has not been made during the year.
A performance evaluation for the CEO has taken place during the financial year in accordance with the evaluation process
disclosed by the Company. This evaluation has been conducted by the Chairman on a quarterly basis during the year with
regard to performance measures set at the commencement of the year.
A performance evaluation for other senior management has been conducted by the CEO during the financial year in ac-
cordance with the evaluation process disclosed by the Company.
Board Roles and Responsibilities
The Board is first and foremost accountable to its shareholders through delivery of timely and balanced disclosures.
The Board sought external guidance to assist the drafting of its “Board Charter” which has been made publicly available on
the Company’s website. This document details the adopted practices and processes in relation to matters reserved for the
Board’s consideration and decision-making. The Board is ultimately responsible for ensuring its actions are in accordance
with key corporate governance principles.
Shareholder Rights
Shareholders are entitled to vote on significant matters impacting on the business, which include the election and remu-
neration of directors and changes to the constitution. Shareholders are strongly encouraged to attend and participate in
the Annual General Meetings of the Company, to lodge questions to be answered by the Board and/or the CEO, and are
able to appoint proxies.
Risk Management
The Board considers identification and management of key risks associated with the business as vital to maximise share-
holder wealth. A yearly assessment of the risk profile of the business is undertaken and reviewed by the Board, covering
all aspects of the business from the operational level through to strategic level risks. The CEO has been delegated the
task of implementing internal controls to identify and manage risks for which the Board provides oversight and is required
to report to the Board on whether such risks are being managed effectively. The effectiveness of the implemented internal
controls is monitored and reviewed regularly. During the year, the CEO has reported to the Board as to the effectiveness of
the Company’s management of its material business risks.
Cellmid 2013 Annual Report 27
Remuneration Policies
The Company’s remuneration committee comprises of the following non-executive directors:
o David King (Chair, independent)
o Graeme Kaufman (independent)
o Martin Rogers (independent)
The remuneration committee reviews the senior executive packages annually by reference to company performance, ex-
ecutive performance, comparable information from industry sectors and other listed companies and independent advice.
Executives may also be entitled to participate in the Company’s employee incentive plan.
The amounts of remuneration for all key management personnel for the Company, including all monetary and non-mon-
etary components, are detailed in the directors’ report under the heading key management personnel compensation. All
remuneration paid to executives is valued at the cost to the Company and expensed. Shares given to executives are valued
as the difference between the market price of those shares and the amount paid by the executive. Options are valued using
the Black-Scholes methodology.
The Board expects that the remuneration structure implemented will result in the Company being able to attract and retain
the best executives to run the consolidated group. It will also provide executives with the necessary incentives to work to
grow long-term shareholder value.
The payment of bonuses, options and other incentive payments are reviewed by the remuneration committee annually as
part of the review of executive remuneration and a recommendation is put to the Board for approval. All bonuses, options
and incentives must be linked to predetermined performance criteria. The Board can exercise its discretion in relation to
approving incentives, bonuses and options and can recommend changes to the committee’s recommendations. Any
changes must be justified by reference to measurable performance criteria.
Remuneration Committee
The names of the members of the remuneration committee and their attendance at meetings of the committee are detailed
in the directors’ report.
The Board has not approved a formal remuneration committee charter and as such, no such charter or summary of such
charter is disclosed on the Company’s website.
There are no schemes for retirement benefits other than statutory superannuation for non-executive directors.
28 Cellmid 2013 Annual Report
Financial
Report
31
32
33
34
35
70
71
Contents
Statements of Profit or Loss and Other Comprehensive Income
Consolidated Statement of Financial Position
Consolidated Statement of Changes in Equity
Consolidated Statement of Cash Flows
Notes to the Financial Statements
Directors' declaration
Independent Auditor's Report
Cellmid 2013 Annual Report 29
Consolidated Statement of
Profit or Loss and Other
Comprehensive Income
For the year ended 30 June 2013
Consolidated Group
Note
3
3
3
Revenue
Other revenue
Other income
Less Expenditure
Cost of sales
Advertisement & marketing expenses
Bad debts
Consultancy expenses
Communication expenses
Depreciation and amortisation expenses
Director's remuneration
Employee benefits expenses
Finance costs
(Gain) / Loss on foreign exchange
Reclassification of impairment loss on available for sale asset
20
Occupancy expenses
Professional fees
Research and development expenses
Share - based compensation
Subscriptions expenses
Travel expenses
Other expenses
Loss before income tax
Income tax benefit
Loss for the year
Other comprehensive income, net of tax
Total comprehensive loss for the year
Net loss attributable to
Owners of Cellmid Limited
Non-controlling interests
Earnings per share for loss attributable to the ordinary equity
holders of the Company
Basic earnings per share (cents)
Diluted earnings per share (cents)
8
8
2013
$
541,649
170,764
48,875
761,288
84,606
214,411
1,227
422,171
37,122
16,634
150,640
885,483
1,124
(13,338)
-
102,058
108,434
475,361
4,032
71,035
201,255
326,206
2012
$
132,826
38,447
-
171,273
33,157
58,454
-
300,122
38,339
11,419
108,350
873,947
39,714
(49,237)
7,090
95,864
164,721
599,047
228,999
88,018
155,674
126,598
3,088,461
2,880,276
4
5
(2,327,173)
(2,709,003)
785,866
736,520
(1,541,307)
(1,972,483)
-
-
(1,541,307)
(1,972,483)
(1,528,041)
(1,970,360)
(13,266)
(2,123)
(1,541,307)
(1,972,483)
Cents
(0.27)
(0.27)
Cents
(0.46)
(0.46)
The above statement of profit or loss and other comprehensive income should be read in conjunction with the accompanying notes
Cellmid 2013 Annual Report 31
Consolidated Statement of
Financial Position
As at 30 June 2013
ASSETS
CURRENT ASSETS
Cash and cash equivalents
Trade and other receivables
Inventories
Other assets
TOTAL CURRENT ASSETS
NON-CURRENT ASSETS
Other financial assets
Plant and equipment
Intangibles assets
TOTAL NON-CURRENT ASSETS
TOTAL ASSETS
LIABILITIES
CURRENT LIABILITIES
Trade and other payables
Provisions
TOTAL CURRENT LIABILITIES
NON-CURRENT LIABILITIES
Provisions
TOTAL NON-CURRENT LIABILITIES
TOTAL LIABILITIES
NET ASSETS
EQUITY
Contributed equity
Reserves
Accumulated Losses
Capital and reserves attributable to owners of Cellmid Limited
Non-controlling interest
TOTAL EQUITY
Note
Consolidated Group
2013
$
2012
$
9
10
11
15
12
13
14
16
17
17
18
19
19
1,754,994
1,050,593
255,695
71,168
1,694,926
1,289,237
73,321
30,638
3,778,936
2,441,636
-
51,633
2,163,150
2,214,783
5,993,719
42,910
32,276
1,440
76,626
2,518,262
501,299
134,755
636,054
52,508
52,508
688,562
258,577
135,448
394,025
34,753
34,753
428,778
5,305,157
2,089,484
25,336,522
20,799,831
1,966,375
1,746,085
(21,969,496)
(20,441,455)
5,333,401
2,104,461
(28,244)
(14,978)
5,305,157
2,089,483
This consolidated statement of financial position should be read in conjunction with the accompanying notes.
32 Cellmid 2013 Annual Report
Consolidated Statement of
Changes in Equity
For the year ended 30 June 2013
Consolidated Group
Attributable to owners of Cellmid Limited
Reserves
General
Reserve
Foreign
exchange
reserve
Available
for Sale
Reserve
Accumu-
lated
Losses
Total
Non-
controlling
interest
Total
equity
Note
Issued
Capital
Share
Based
Payments
Reserve
$
$
Balance at 1 July 2011
18,838,712
1,660,231
Loss for the year as reported in
the 2011 financial statements
Other comprehensive income
Total comprehensive income
for the year 30 June 2012
Transactions with equity
holders:
Contributions of equity
Share based compensation
Movement in share based
payment reserve
Movement in available for sale
reserve
Net movement as a result of
shares issued to minority interest
-
-
-
1,805,120
156,000
-
-
-
-
-
-
-
-
62,999
-
-
$
-
-
-
-
(11,005)
-
-
-
33,860
Total
1,961,120
62,999
22,855
Balance at 30 June 2012
18 & 19
20,799,832
1,723,230
22,855
Balance at 1 July 2012
20,799,832
1,723,230
22,855
Loss for the year as reported in
the 2013 financial statements
Other comprehensive income
Total comprehensive income
for the year 30 June 2013
Transactions with equity
holders:
-
-
-
Contributions of equity
4,536,690
Share based compensation
Movement in share based
payment reserve
Movement in available for sale
reserve
Movement in foreign exchange
reserve
Net movement as a result of
shares issued to minority interest
-
-
-
-
-
-
-
-
-
4,033
-
-
-
-
Total
4,536,690
4,033
-
-
-
-
-
-
-
-
-
-
$
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
216,257
-
216,257
$
$
$
10,120
(18,471,095)
2,037,968
$
-
$
2,037,968
-
(1,970,360)
(1,970,360)
(2,123)
(1,972,483)
-
-
-
-
-
-
(1,970,360)
(1,970,360)
(2,123)
(1,972,483)
-
-
-
(10,120)
-
-
-
-
-
-
1,794,115
21,005
1,815,120
156,000
62,999
(10,120)
-
-
-
156,000
62,999
(10,120)
33,860
(33,860)
-
(10,120)
(1,970,360)
66,494
(14,978)
51,516
-
(20,441,455)
2,104,462
(14,978)
2,089,484
-
-
-
(20,441,455)
2,104,462
(14,978)
2,089,484
(1,528,041)
(1,528,041)
(13,266)
(1,541,307)
-
-
-
-
-
(1,528,041)
(1,528,041)
(13,266)
(1,541,307)
-
-
-
-
-
-
-
-
-
-
-
-
-
4,536,690
4,033
-
-
216,257
-
-
-
-
-
-
-
4,536,690
4,033
-
-
216,257
-
-
4,756,980
-
4,756,980
Balance at 30 June 2013
18 & 19
25,336,522
1,727,263
22,855
216,257
-
(21,969,496)
5,333,401
(28,244)
5,305,157
This statement of changes in equity should be read in conjunction with the accompanying notes.
Cellmid 2013 Annual Report 33
Consolidated Statement of
Cash Flows
For the year ended 30 June 2013
CASH FLOWS FROM OPERATING ACTIVITIES
Receipts (inclusive of GST)
Payments to suppliers and employees (inclusive of GST)
Research and development expenses
Interest received
Income tax benefit
Other grant income
Finance costs
Net cash used in operating activities
CASH FLOWS FROM INVESTING ACTIVITIES
Payment for acquisition of subsidiary, net of cash acquired
Proceeds on sale of financial asset
Purchase of non-current assets
Net cash used in investing activities
CASH FLOWS FROM FINANCING ACTIVITIES
Proceeds from issue of shares (net of share issue costs)
Repayment of borrowings
Net cash provided by financing activities
Net increase / (decrease) in cash held
Cash and cash equivalents at beginning of financial year
Effect of exchange rate changes
Consolidated Group
2013
$
2012
$
Note
20
28
644,080
116,225
(2,552,229)
(1,977,623)
(475,361)
30,833
785,866
115,167
(1,124)
(599,047)
5,370
736,520
-
(39,714)
(1,452,768)
(1,758,269)
(803,911)
91,785
(26,734)
(738,860)
-
-
(31,931)
(31,931)
2,864,561
-
2,864,561
672,933
1,805,120
(556,835)
1,248,285
(541,915)
1,050,593
1,592,508
31,468
-
Cash and cash equivalents at end of financial year
9
1,754,994
1,050,593
This statement of cash flows should be read in conjunction with the accompanying notes.
34 Cellmid 2013 Annual Report
Notes to the
Financial Statements
Contents
1 Summary of Significant Accounting Policies
2 Parent Information
3 Revenue and Other Revenue
4 Profit/(Loss) for the year
5
Income Tax Expense
6
Interests of Key Management Personnel (KMP)
7 Auditor’s Remuneration
8 Earnings per Share
9 Cash and Cash Equivalents
10 Trade and Other Receivables
11
Inventories
12 Other Financial Assets
13 Plant and Equipment
14
Intangible Assets
15 Other Assets
16 Trade and Other Payables
17 Provisions
18 Contributed Equity
19 Reserves and Accumulated Losses
20 Cash Flow Information
21 Critical Accounting Estimates and Judgements
22 Events after the Reporting Period
23 Related Party Transactions
24 Financial Risk Management
25 Subsidiary and Transactions with non-controlling Interest
26 Segment Information
27 Commitments
28 Business Combinations
29 Contigent Liabilities
30 Company Details
36
45
46
46
47
48
51
51
52
52
53
53
54
54
55
55
55
56
60
61
62
62
62
63
65
65
68
68
69
69
Cellmid 2013 Annual Report 35
Notes to the Financial Statements
Continued
NOTE 1: SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Statement of compliance
The company is a public company, listed on the Australian Stock Exchange. It is incorporated in Australia and is domiciled
in Australia.
The financial statements are general purpose financial statements that have been prepared in accordance with Austral-
ian Accounting Standards, Australian Accounting Interpretations, other authoritative pronouncements of the Australian
Accounting Standards Board (AASB) and the Corporations Act 2001, as appropriate for-profit oriented entities. These
financial statements also comply with International Financial Reporting Standards as issued by the International Accounting
Standards Board (IASB)
The financial statements comprise the consolidated financial statements of the Group.
The financial statements were authorised for issue by the directors on 28 August 2013.
Basis of Preparation
The financial statements have been prepared on an accruals basis and are based on historical costs, except for certain
non-current assets and financial instruments that are measured at re-valued amounts or fair values, as explained in the
accounting policies below. Historical cost is generally based on the fair values of the consideration given in exchange for
assets. All amounts are presented in Australian dollars, unless otherwise noted.
The preparation of financial statements in conformity with AIFRS requires the use of certain accounting estimates. It also
requires management to exercise its judgement in the process of applying the group’s accounting policies. The areas
involving a higher degree of judgement or complexity, or areas where assumptions and estimates are significant to the
financial statements, are disclosed in Note 21.
New, revised or amending Accounting Standards and Interpretations adopted
The Group has adopted all of the new, revised or amending Accounting Standards and Interpretations issued by the Aus-
tralian Accounting Standards Board (‘AASB’) that are mandatory for the current reporting period.
Any new, revised or amending Accounting Standards or Interpretations that are not yet mandatory have not been early
adopted.
Any significant impact on the accounting policies of the Group from the adoption of these Accounting Standards and
Interpretations are disclosed below. The adoption of these Accounting Standards and Interpretations did not have any
significant impact on the financial performance or position of the Group.
The following Accounting Standards and Interpretations are most relevant to the Group:
AASB 2011-9 Amendments to Australian Accounting Standards - Presentation of Items of Other Comprehensive Income
The Group has applied AASB 2011-9 amendments from 1 July 2012. The amendments requires grouping together of
items within other comprehensive income on the basis of whether they will eventually be ‘recycled’ to the profit or loss
(reclassification adjustments). The change provides clarity about the nature of items presented as other comprehensive
income and the related tax presentation. The amendments also introduced the term ‘Statement of profit or loss and other
comprehensive income’ clarifying that there are two discrete sections, the profit or loss section (or separate statement of
profit or loss) and other comprehensive income section.
36 Cellmid 2013 Annual Report
a. Going Concern
The Directors have prepared the financial statements on a going concern basis, which contemplates continuity of normal
business activities and the realisation of assets and the settlement of liabilities in the ordinary course of business. Based on
anticipated levels of operational cash flow, the Group has sufficient cash to fund current operations for more than one year.
b. Principles of Consolidation
The consolidated financial statements incorporate the assets, liabilities and results of entities controlled by Cellmid Limited
at the end of the reporting period. A controlled entity is any entity over which Cellmid Limited has the ability and right to
govern the financial and operating policies so as to obtain benefits from the entity’s activities.
Income and expenses of subsidiaries acquired or disposed of during the year are included in the consolidated statement
of profit or loss and other comprehensive income from the effective date of acquisition and up to the effective date of dis-
posal, as appropriate. Total comprehensive income of subsidiaries is attributed to the owners of the company and to the
non-controlling interests even if this results in the non-controlling interest having a deficit balance.
Where necessary, adjustments are made to the financial statements of subsidiaries to bring their accounting policies into
line with those used by other members of the group.
All intra-group transactions, balances, income and expenses are eliminated in full on consolidation.
c. Segment Reporting
Operating segments are reported in a manner consistent with the internal reporting provided to the chief operating decision
maker. The chief operating decision makers, who are responsible for allocating resources and assessing performance of
the operating segments, is the Board of Directors.
d. Revenue and Other Income Recognition
Revenue is measured at the fair value of the consideration received or receivable after taking into account any trade
discounts and volume rebates allowed. Revenue from the sale of goods is recognised at the point of delivery as this cor-
responds to the transfer of significant risks and rewards of ownership of the goods and the cessation of all involvement in
those goods.
Interest revenue is recognised using the effective interest rate method.
Royalties determined on a time basis are recognised on a straight-line basis over the period of the agreement. Government
grants are recognised in profit and loss on a systematic basis over the periods in which the Group recognises as expenses
the related costs for which the grants are intended to compensate, but not before the receipt of the grant is relatively certain.
e. Income Tax
The income tax expense (revenue) for the period is the tax payable on the current period’s taxable income based on the
national income tax rate for each jurisdiction adjusted by changes in deferred tax assets and liabilities attributable to tem-
porary differences between the tax bases of assets and liabilities and their carrying amounts in the financial statements,
and to unused tax losses.
Deferred tax assets and liabilities are calculated at the tax rates that are expected to apply to the period when the asset is
realised or the liability is settled and their measurement also reflects the manner in which management expects to recover
or settle the carrying amount of the related asset or liability.
Deferred tax assets relating to temporary differences and unused tax losses are recognised only to the extent that it is prob-
able that future taxable profit will be available against which the benefits of the deferred tax asset can be utilised.
Cellmid 2013 Annual Report 37
Notes to the Financial Statements
Continued
Current tax assets and liabilities are offset where a legally enforceable right of set-off exists and it is intended that net set-
tlement or simultaneous realisation and settlement of the respective asset and liability will occur. Deferred tax assets and
liabilities are offset where: (a) a legally enforceable right of set-off exists; and (b) the deferred tax assets and liabilities relate
to income taxes levied by the same taxation authority on either the same taxable entity or different taxable entities where
it is intended that net settlement or simultaneous realisation and settlement of the respective asset and liability will occur
in future periods in which significant amounts of deferred tax assets or liabilities are expected to be recovered or settled.
f. Cash and Cash Equivalents
Cash and cash equivalents include cash on hand, deposits available on demand with banks, other short-term highly liquid
investments with original maturities of three months or less, and bank overdrafts. Bank overdrafts are reported within short-
term borrowings in current liabilities in the statement of financial position.
g. Receivables
Receivables are recognised initially at fair value and subsequently measured at amortised cost, less provision for doubtful
debts.
Collectability of receivables is reviewed on an ongoing basis. Debts which are known to be uncollectible are written off. A
provision for doubtful receivables is established when there is objective evidence that the Group will not be able to collect
all amounts due according to the original terms of receivables.
h. Inventories
Inventories are measured at the lower of cost and net realisable value. The cost of manufactured products includes direct
materials, direct labour and an appropriate portion of variable and fixed overheads. Overheads are applied on the basis of
normal operating capacity. Costs are assigned on the basis of weighted average costs. Costs of purchased inventory are
determined after deducting rebates and discounts. Net realisable value is the estimated selling price in the ordinary course
of business less the estimated costs of completion and the estimated cost necessary to make the sale.
i. Plant and Equipment
Plant and equipment are measured on the cost basis and therefore carried at cost less accumulated depreciation and any
accumulated impairment.
The cost of fixed assets constructed within the Group includes the cost of materials, direct labour, borrowing costs and an
appropriate proportion of fixed and variable overheads.
Subsequent costs are included in the asset’s carrying amount or recognised as a separate asset, as appropriate, only when
it is probable that future economic benefits associated with the item will flow to the group and the cost of the item can be
measured reliably. All other repairs and maintenance are charged to the statement of profit or loss and other comprehen-
sive income during the financial period in which they are incurred.
Depreciation
The depreciable amount of all fixed assets is depreciated on a straight-line basis over the asset’s useful life to the Group
commencing from the time the asset is held ready for use. Leasehold improvements are depreciated over the shorter of
either the unexpired period of the lease or the estimated useful lives of the improvements.
The depreciation rates used for each class of depreciable assets are:
Class of Fixed Asset
Furniture and fittings
Office equipment
Depreciation Rate
20%
6.7-33.33%
The assets’ residual values and useful lives are reviewed, and adjusted if appropriate, at the end of each reporting period.
An asset’s carrying amount is written down immediately to its recoverable amount if the asset’s carrying amount is greater
than its estimated recoverable amount.
38 Cellmid 2013 Annual Report
Gains and losses on disposals are determined by comparing proceeds with the carrying amount. These gains and losses
are included in the statement of profit or loss and other comprehensive income. When revalued assets are sold, amounts
included in the revaluation surplus relating to that asset are transferred to retained earnings.
j.
Investments and Other Financial Assets
The Group classified its investments in the following categories: loans and receivables and available for sale financial assets.
The classification depends on the nature and purpose of the investment and is determined at the time of initial recognition.
(i) Loans and receivables
Loans and receivables are non-derivative financial assets with fixed or determinable payments that are not quoted in
an active market and are subsequently measured at amortised cost.
Loans and receivables are included in current assets, where they are expected to mature within 12 months after the
end of the reporting period.
Loan and receivables are measured at amortised cost using the effective interest method, less any impairment. Interest
income is recognised by applying the effective interest rate, except for short-term receivables when the recognition of
interest would be immaterial.
(ii) Available-for-sale financial assets
Listed shares and listed redeemable notes held by the group that are traded in an active market are classified as
available-for-sale financial assets and are stated at fair value.
Gains and losses arising from changes in fair value are recognised in other comprehensive income and accumulated
in the investments revaluation reserve.
Where the investment is disposed of or is determined to be impaired, the cumulative gain or loss previously
accumulated in the investment revaluation reserve is reclassified to profit and loss. The fair value of available-for-
sale assets denominated in a foreign currency is determined in that foreign currency and translated at the spot rate
at the end of the reporting period. The foreign exchange gains and losses that are recognised in profit and loss are
determined based on the amortised cost of the monetary asset. Other foreign gains and losses are recognised in other
comprehensive income.
k. Intangibles Other than Goodwill
Patents and trademarks
Patents and trademarks are recognised at cost of acquisition. Patents and trademarks have a finite life and are carried at
cost less any accumulated amortisation and any impairment losses. The Group has determined the useful life of the intan-
gible assets at 20 years. There is no amortisation charge to the intangible assets in the 2013 financial Year.
Research and development
Expenditure on research activities is recognised as an expense in the period in which is incurred.
Expenditure on development projects (relating to the design and testing of new or improved products) are capitalised as
intangible assets when it is probable that the project will be a success considering its commercial and technical feasibility
and its costs can be measured reliably. The expenditure capitalised comprises all directly attributable costs, including costs
of materials, services, direct labour and an appropriate proportion of overheads. Development expenditures that do not
meet these criteria are recognised as an expense as incurred. Development costs previously recognised as an expense are
not recognised as an asset in a subsequent period.
Cellmid 2013 Annual Report 39
Notes to the Financial Statements
Continued
I.
Impairment of Assets
At the end of each reporting period, the Group assesses whether there is any indication that an asset may be impaired.
The assessment will include the consideration of external and internal sources of information including dividends received
from subsidiaries, associates or jointly controlled entities deemed to be out of pre-acquisition profits. If such an indication
exists, an impairment test is carried out on the asset by comparing the recoverable amount of the asset, being the higher
of the asset’s fair value less costs to sell and value in use, to the asset’s carrying amount. Any excess of the asset’s carrying
amount over its recoverable amount is recognised immediately in profit or loss, unless the asset is carried at a re-valued
amount in accordance with another Standard (e.g. in accordance with the revaluation model in AASB 116). Any impairment
loss of a re-valued asset is treated as a revaluation decrease in accordance with that other Standard.
Where it is not possible to estimate the recoverable amount of an individual asset, the Group estimates the recoverable
amount of the cash-generating unit to which the asset belongs.
Impairment testing is performed annually for goodwill and intangible assets with indefinite lives.
m. Trade and Other Payables
These amounts represent liabilities for goods and services provided to the Group prior to the end of financial year which are
unpaid. The amounts are unsecured and are usually paid within 30 days of recognition.
n. Provisions
Provisions are recognised when the Group has a legal or constructive obligation, as a result of past events, for which it is
probable that an outflow of economic benefits will result and that outflow can be reliably measured.
Provisions are measured using the best estimate of the amounts required to settle the obligation at the end of the reporting
period.
o. Employee Benefits
Provision is made for the Group’s liability for employee benefits arising from services rendered by employees to the end
of the reporting period. Employee benefits that are expected to be settled within the income year have been measured at
the amounts expected to be paid when the liability is settled. In determining the liability, consideration is given to employee
wages increases and the probability that the employee may satisfy vesting requirements.
Wages and salaries, annual leave and sick leave
Liability for wages and salaries, including non monetary benefits, annual leave and accumulating sick leave expected to be
settled within 12 months of the reporting date are recognised in other payables in respect of employees’ services up to the
reporting date and are measured at the amounts expected to be paid when the liabilities are settled.
Long service leave
Liability for long service leave is recognised in the provision for employee benefits and measured as the present value of
expected future payments to be made in respect of services provided by employees up to the reporting date using the
projected unit credit method. Consideration is given to expected future wage and salary levels, experience of employee
departures and period of service.
Retirement benefit obligations
Contributions to the defined contribution fund are recognised as an expense as they become payable. Prepaid contribu-
tions are recognised as an asset to the extent that a cash refund or a reduction in the future payment is available. Contribu-
tions are paid into the fund nominated by the employee.
40 Cellmid 2013 Annual Report
Share-based payments
The fair value of options granted is recognised as a benefit expense with a corresponding increase in equity. The fair value
is measured at grant date and recognised over the period during which the directors and executives become uncondition-
ally entitled to the options.
The fair value at grant date is determined using binomial option pricing model that takes into account the exercise price,
the term of option, the impact of dilution, the share price at grant date and expected price volatility of the underlying share,
the expected dividend yield and the risk free interest rate for the term of the option.
The fair value of the options granted is adjusted to reflect market vesting conditions, but excludes the impact of any non
market vesting conditions. Non market vesting conditions are included in assumptions about the number of options that
are expected to become exercisable. The benefit expense recognised each period takes into account the most recent
estimate.
Upon the exercise of options, the balance of the share based payments reserve relating to those options is transferred to
share capital and the proceeds received, net of any directly attributable transaction costs, are credited to share capital.
p. Equity-settled compensation
The Group operates an employee share ownership plan. Share-based payments to employees are measured at the fair
value of the instruments issued and amortised over the vesting periods. Share-based payments to non-employees are
measured at the fair value of goods or services received or the fair value of the equity instruments issued, if it is determined
the fair value of the goods or services cannot be reliably measured, and are recorded at the date the goods or services are
received. The corresponding amount is recorded to the option reserve. The fair value of options is determined using the
binominal pricing model. The number of shares and options expected to vest is reviewed and adjusted at the end of each
reporting period such that the amount recognised for services received as consideration for the equity instruments granted
is based on the number of equity instruments that eventually vest.
Upon the exercise of options, the balance of the share based payments reserve relating to those options is transferred to
share capital and the proceeds received, net of any directly attributable transaction costs, are credited to share capital.
q. Functional and Presentation Currency
The functional currency of each of the Group’s entities is measured using the currency of the primary economic environ-
ment in which that entity operates. The consolidated financial statements are presented in Australian dollars which is the
parent entity’s functional and presentation currency.
Foreign currency transactions
Foreign currency transactions are translated into Australian dollars using the exchange rates prevailing at the dates of the
transactions. Foreign exchange gains and losses resulting from the settlement of such transactions and from the translation
at financial year-end exchange rates of monetary assets and liabilities denominated in foreign currencies are recognised in
profit or loss.
Foreign operations
The assets and liabilities of foreign operations are translated into Australian dollars using the exchange rates at the reporting
date. The revenues and expenses of foreign operations are translated into Australian dollars using the average exchange
rates, which approximate the rate at the date of the transaction, for the period. All resulting foreign exchange differences
are recognised in other comprehensive income through the foreign currency reserve in equity.
The foreign currency reserve is recognised in profit or loss when the foreign operation or net investment is disposed.
Cellmid 2013 Annual Report 41
Notes to the Financial Statements
Continued
r. Goods and Services Tax (GST)
Revenues, expenses and assets are recognised net of the amount of GST, except where the amount of GST incurred is not
recoverable from the Australian Taxation Office (ATO).
Receivables and payables are stated inclusive of the amount of GST receivable or payable. The net amount of GST recover-
able from, or payable to, the ATO is included with other receivables or payables in the statement of financial position.
Cash flows are presented on a gross basis. The GST components of cash flows arising from investing or financing activi-
ties which are recoverable from, or payable to, the ATO are presented as operating cash flows included in receipts from
customers or payments to suppliers.
s. Business Combinations
The acquisition method of accounting is used to account for business combinations regardless of whether equity instru-
ments or other assets are acquired.
The consideration transferred is the sum of the acquisition-date fair values of the assets transferred, equity instruments
issued or liabilities incurred by the acquirer to former owners of the acquiree and the amount of any non-controlling inter-
est in the acquiree. For each business combination, the non-controlling interest in the acquiree is measured at either fair
value or at the proportionate share of the acquiree’s identifiable net assets. All acquisition costs are expensed as incurred
to profit or loss.
On the acquisition of a business, the Group assesses the financial assets acquired and liabilities assumed for appropriate
classification and designation in accordance with the contractual terms, economic conditions, the Group’s operating or
accounting policies and other pertinent conditions in existence at the acquisition-date.
Where the business combination is achieved in stages, the Group remeasures its previously held equity interest in the
acquiree at the acquisition-date fair value and the difference between the fair value and the previous carrying amount is
recognised in profit or loss.
Contingent consideration to be transferred by the acquirer is recognised at the acquisition-date fair value. Subsequent
changes in the fair value of contingent consideration classified as an asset or liability is recognised in profit or loss. Con-
tingent consideration classified as equity is not remeasured and its subsequent settlement is accounted for within equity.
The difference between the acquisition-date fair value of assets acquired, liabilities assumed and any non¬controlling inter-
est in the acquiree and the fair value of the consideration transferred and the fair value of any pre¬existing investment in
the acquiree is recognised as goodwill. If the consideration transferred and the pre-existing fair value is less than the fair
value of the identifiable net assets acquired, being a bargain purchase to the acquirer, the difference is recognised as a
gain directly in profit or loss by the acquirer on the acquisition-date, but only after a reassessment of the identification and
measurement of the net assets acquired, the non-controlling interest in the acquiree, if any, the consideration transferred
and the acquirer’s previously held equity interest in the acquirer.
Business combinations are initially accounted for on a provisional basis. The acquirer retrospectively adjusts the provisional
amounts recognised and also recognises additional assets or liabilities during the measurement period, based on new in-
formation obtained about the facts and circumstances that existed at the acquisition-date. The measurement period ends
on either the earlier of (i) 12 months from the date of the acquisition or (ii) when the acquirer receives all the information
possible to determine fair value.
t. Earnings per Share
Basic earnings per share
Basic earnings per share is calculated by dividing the profit attributable to the owners of Cellmid Limited, excluding any
costs of servicing equity other than ordinary shares, by the weighted average number of ordinary shares outstanding during
the financial year, adjusted for bonus elements in ordinary shares issued during the financial year.
42 Cellmid 2013 Annual Report
Diluted earnings per share
Diluted earnings per share adjusts the figures used in the determination of basic earnings per share to take into account
the after income tax effect of interest and other financing costs associated with dilutive potential ordinary shares and the
weighted average number of shares assumed to have been issued for no consideration in relation to dilutive potential or-
dinary shares.
u. Comparative Figures
When required by Accounting Standards, comparative figures have been adjusted to conform to changes in presentation
for the current financial year.
Where the group has retrospectively applied an accounting policy, made a retrospective restatement of items in the financial
statements or reclassified items in its financial statements, an additional statement of financial position as at the beginning
of the earliest comparative period will be disclosed.
v. Rounding of Amounts
The parent entity has applied the relief available to it under ASIC Class Order 98/100 and accordingly, amounts in the finan-
cial statements and directors’ report have been rounded off to the nearest $1.
w. New Accounting Standards for Application in Future Periods
The AASB has issued new and amended Accounting Standards and Interpretations that have mandatory application dates
for future reporting periods and which the group has decided not to early adopt. A discussion of those future requirements
as they apply to the group and their impact on the group is as follows:
– AASB 10 Consolidated Financial Statements
This standard is applicable to annual reporting periods beginning on or after 1 January 2013. The standard has a new
definition of ‘control’. Control exists when the reporting entity is exposed, or has the rights, to variable returns (e.g.
dividends, remuneration, returns that are not available to other interest holders including losses) from its involvement
with another entity and has the ability to affect those returns through its ‘power over that other entity. A reporting entity
has power when it has rights (e.g. voting rights, potential voting rights, rights to appoint key management, decision
making rights, kick out rights) that give it the current ability to direct the activities that significantly affect the investee’s
returns (e.g. operating policies, capital decisions, appointment of key management). The Group will not only have to
consider its holdings and rights but also the holdings and rights of other shareholders in order to determine whether
it has the necessary power for consolidation purposes. The adoption of this standard from 1 July 2013 may have
an impact where the Group has a holding of less than 50% in an entity, has de facto control, and is not currently
consolidating that entity.
– AASB 12 Disclosure of Interests in Other Entities
This standard is applicable to annual reporting periods beginning on or after 1 January 2013. It contains the entire
disclosure requirement associated with other entities, being subsidiaries, associates and joint ventures. The disclosure
requirements have been significantly enhanced when compared to the disclosures previously located in AASB 127
‘Consolidated and Separate Financial Statements’, AASB 128 ‘Investments in Associates’, AASB 131 ‘Interests in
Joint Ventures’ and Interpretation 112 ‘Consolidation - Special Purpose Entities’. The adoption of this standard from
1 July 2013 will significantly increase the amount of disclosures required to be given by the Group such as significant
judgements and assumptions made in determining whether it has a controlling or non¬controlling interest in another
entity and the type of non-controlling interest and the nature and risks involved.
Cellmid 2013 Annual Report 43
Notes to the Financial Statements
Continued
– AASB 13 Fair Value Measurement and AASB 2011-8 Amendments to Australian Accounting Standards arising
from AASB 13
This standard and its consequential amendments are applicable to annual reporting periods beginning on or after 1
January 2013. The standard provides a single robust measurement framework, with clear measurement objectives, for
measuring fair value using the ‘exit price’ and it provides guidance on measuring fair value when a market becomes
less active. The ‘highest and best use’ approach would be used to measure assets whereas liabilities would be based
on transfer value. As the standard does not introduce any new requirements for the use of fair value, its impact on
adoption by the Group from 1 July 2013 should be minimal, although there will be increased disclosures where fair
value is used.
– AASB 119 Employee Benefits (September 2011) and AASB 2011-10 Amendments to Australian Accounting
Standards arising from AASB 119 (September 2011)
This revised standard and its consequential amendments are applicable to annual reporting periods beginning on or
after 1 January 2013. The amendments make changes to the accounting for defined benefit plans and the definition of
short-term employee benefits, from ‘due to’ to ‘expected to’ be settled within 12 months. The later will require annual
leave that is not expected to be wholly settled within 12 months to be discounted allowing for expected salary levels
in the future period when the leave is expected to be taken. The adoption of the revised standard from 1 July 2013 is
expected to reduce the reported annual leave liability of the Group.
– AASB 2011-4 Amendments to Australian Accounting Standards to Remove Individual Key Management
Personnel Disclosure Requirement
These amendments are applicable to annual reporting periods beginning on or after 1 July 2013, with early adoption
not permitted. They amend AASB 124 ‘Related Party Disclosures’ by removing the disclosure requirements for
individual key management personnel (XIVIR). The adoption of these amendments from 1 July 2014 will remove the
duplication of information relating to individual KMP in the notes to the financial statements and the directors report.
As the aggregate disclosures are still required by AASB 124 and during the transitional period the requirements may
be included in the Corporations Act or other legislation, it is expected that the amendments will not have a material
impact on the Group.
– AASB 2011-7 Amendments to Australian Accounting Standards arising from the Consolidation and Joint
Arrangements Standards
The amendments are applicable to annual reporting periods beginning on or after 1 January 2013. The amendments
make numerous consequential changes to a range of Australian Accounting Standards and Interpretations, following the
issuance of AASB 10, AASB 11, AASB 12 and revised AASB 127 and AASB 128. The adoption of these amendments
from 1 July 2013 will not have a material impact on the Group.
– AASB 2012-5 Amendments to Australian Accounting Standards arising from Annual Improvements 2009-
2011 Cycle
The amendments are applicable to annual reporting periods beginning on or after 1 January 2013. The amendments
affect five Australian Accounting Standards as follows: Confirmation that repeat application of AASB 1 (IFRS 1) ‘First-
time Adoption of Australian Accounting Standards’ is permitted; Clarification of borrowing cost exemption in AASB
1; Clarification of the comparative information requirements when an entity provides an optional third column or is
required to present a third statement of financial position in accordance with AASB 101 ‘Presentation of Financial
Statements; Clarification that servicing of equipment is covered by AASB 116 ‘Property, Plant and Equipment’, if
such equipment is used for more than one period; clarification that the tax effect of distributions to holders of equity
instruments and equity transaction costs in AASB 132 ‘Financial Instruments: Presentation’ should be accounted for
in accordance with AASB 112 ‘Income Taxes’; and clarification of the financial reporting requirements in AASB 134
‘Interim Financial Reporting’ and the disclosure requirements of segment assets and liabilities. The adoption of the
amendments from 1 July 2013 will not have a material impact on the Group.
44 Cellmid 2013 Annual Report
– AASB 2012-9 Amendment to AASB 1048 arising from the Withdrawal of Australian Interpretation 1039
This amendment is applicable to annual reporting periods beginning on or after 1 January 2013. The amendment
removes reference in AASB 1048 following the withdrawal of Interpretation 1039. The adoption of this amendment will
not have a material impact on the Group.
– AASB 2012-10 Amendments to Australian Accounting Standards - Transition Guidance and Other Amendments
These amendments are applicable to annual reporting periods beginning on or after 1 January 2013. They amend
AASB 10 and related standards for the transition guidance relevant to the initial application of those standards. The
amendments clarify the circumstances in which adjustments to an entity’s previous accounting for its involvement with
other entities are required and the timing of such adjustments. The adoption of these amendments will not have a
material impact on the Group.
NOTE 2: PARENT INFORMATION
STATEMENT OF FINANCIAL POSITION
ASSETS
Current assets
TOTAL ASSETS
LIABILITIES
Current liabilities
TOTAL LIABILITIES
NET ASSETS
EQUITY
Contributed equity
Accumulated losses
Share based payment reserve
TOTAL EQUITY
STATEMENT OF PROFIT OR LOSS AND OTHER COMPREHENSIVE INCOME
Loss of the parent entity
Total comprehensive loss
2013
$
2012
$
2,500,986
6,273,428
2,719,856
2,794,729
480,084
532,593
380,914
415,667
5,740,835
2,379,062
25,273,651
20,799,832
(21,317,677)
(20,144,000)
1,784,862
5,740,836
1,733,350
2,389,182
(1,173,677)
(1,173,677)
(1,842,581)
(1,842,581)
Cellmid 2013 Annual Report 45
Notes to the Financial Statements
Continued
NOTE 3: REVENUE AND OTHER INCOME
Consolidated Group
2013
$
2012
$
541,649
541,649
132,826
132,826
30,833
115,167
24,000
358
406
170,764
712,413
48,875
48,875
5,370
-
24,000
704
8,373
38,447
171,273
-
-
Consolidated Group
2013
$
2012
$
(84,606)
(1,124)
(33,157)
(39,714)
(813,602)
(810,563)
(71,880)
13,338
(63,384)
49,237
(95,842)
(91,176)
(16,634)
(475,361)
(11,419)
(599,047)
Revenue from continuing operations
Sales revenue:
– sale of goods
Other revenue:
– interest received
– government grants received
– rental revenue
– royalties
– other revenue
Total revenue
Other income:
– Gain on disposal of financial assets
Total other income
NOTE 4: LOSS FOR THE YEAR
Loss before income tax from continuing operations includes the following
specific expenses:
Cost of sales
Finance cost
Employee benefits expense
Defined contribution superannuation expenses
Foreign currency translation gain/(losses)
Rental expense on operating leases:
– minimum lease payments
Depreciation and amortisation
– Plant and equipment
Research and development expense
46 Cellmid 2013 Annual Report
NOTE 5: INCOME TAX EXPENSE
a. The components of tax expense comprise:
– Income tax benefit
b. Numerical reconciliation of income tax expense to
Loss before income tax expense
Prima facie tax benefit on loss from ordinary activities
before income tax at 30% (2012: 30%)
A: Add:
Tax effect of:
– Research and development expenditure
– Share based payment
– Deduction on un-deducted & R&D core technology expenditure
– Impairment loss on asset revaluation
– Sundry items
Adjusted income tax
Consolidated Group
2013
$
2012
$
785,866
785,866
736,520
736,520
(2,327,173)
(2,709,003)
(698,152)
(812,701)
396,695
1,210
(190,438)
-
6,406
213,873
(484,279)
523,910
68,700
(190,438)
2,127
13,313
417,612
(395,089)
Tax losses not brought to account
484,279
395,089
Research and development tax benefit
785,866
736,520
Income tax benefit
785,866
736,520
A $785,866 (2012 $736,520) research and development tax offset was received for a claim in accordance with the Com-
monwealth Governments Research and Development Tax Incentive.
c. Tax losses
Carried forward unused tax losses
Current unused tax losses for which no deferred tax asset
has been recognised
Total
Potential future tax benefit at notional tax rate 30%
All unused tax losses were incurred by Australian entities.
This income tax benefit arose from losses will only be obtained if:
11,853,317
10,536,355
1,614,264
1,316,962
13,467,581
11,853,317
4,040,274
3,555,995
i
The group derives future assessable income of a nature and of an amount sufficient to enable to benefit from the
deductions for the losses to be realised;
ii. The group continues to comply with the conditions for deductibility imposed by tax legislation; and
iii. No changes in tax legislation adversely affect the consolidated entity in realising the benefit from the deductions
for the losses.
Cellmid 2013 Annual Report 47
Notes to the Financial Statements
Continued
d. As Advangen International Pty Ltd ceased to be a wholly owned subsidiary of Cellmid Limited on 13 March 2012, it
ceased to be part of the tax consolidated group from that date.
NOTE 6: INTERESTS OF KEY MANAGEMENT PERSONNEL (KMP)
a. Directors and key management personnel
The following persons were directors or key management personnel of Cellmid Limited during the financial year.
David King (Chairman) - appointed from 18 January 2008 to current
Ms Maria Halasz (Chief Executive Officer) - appointed from 19 November 2007 to current
Mr Robin Beaumont (Non executive) - appointed from 12 October 2009 to 27 August 2012
Mr Graeme Kaufman (Non executive) - appointed from 27 August 2012 to current
Mr Martin Rogers (Non executive) - appointed from 19 September 2012 to current
Mr Nicholas Falzon (Secretary and Financial Controller) - appointed from 6 October 2010 to current
Mr Andrew Bald (Secretary) - appointed from 6 August 2012 to 8 April 2013
Ms Jillian McGregor (Secretary) - appointed from 16 July 2013 to current
b. Directors and key management personnel compensation
Refer to the remuneration report contained in the directors’ report for details of the remuneration paid or payable to each
member of the Group’s key management personnel for the year ended 30 June 2013.
The totals of remuneration paid to KMP of the company and the Group during the year are as follows:
Short - term employee benefits
Post - employment benefits
Share - based payments
2013
$
536,887
44,915
-
581,802
2012
$
495,000
41,850
72,999
609,849
c. Equity instrument disclosures relating to key management personnel
Options provided as remuneration and shares issued on exercise of such options
Details of options provided as remuneration, together with terms and conditions of the options, can be found in note 18.
48 Cellmid 2013 Annual Report
(i) KMP Options Holdings
The numbers of options over ordinary shares in the Company held during the financial year by each director of Cellmid
Limited and other key management personnel of the group, including their personally related parties, are set out as table
below.
30 June 2013
Balance at
Beginning
of the Year
Granted as
remuneration
during the
Year
Exercised
during the
Year
Other
Changes
during the
Year
Balance at
end of Year
Vested and
Exercisable
at the end
of the Year
Directors of Cellmid Limited
M Halasz
D King
R Beaumont
G Kaufman
M Rogers
17,000,000
-
3,971,962
Other key management personnel
J McGregor
N Falzon
A Bald
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
(637,375)
16,362,625
16,362,625
11,250,000
11,250,000
11,250,000
-
3,971,962
3,971,962
1,000,000
1,000,000
1,000,000
44,000,000
44,000,000
44,000,000
-
-
-
-
-
-
-
-
-
Maria Halasz owns 16,362,625 options indirectly.
David King owns 11,250,000 options indirectly.
Martin Rogers owns 44,000,000 options indirectly.
30 June 2012
Balance at
Beginning
of the Year
Granted as
remuneration
during the
Year
Exercised
during the
Year
Other
Changes
during the
Year
Balance at
end of Year
Vested and
Exercisable
at the end
of the Year
Directors of Cellmid Limited
M Halasz
D King
R Beaumont
Other key management personnel
N Falzon
(ii) KMP Shareholdings
12,000,000
5,000,000
-
-
-
-
3,971,962
-
-
-
-
-
-
-
-
-
17,000,000
17,000,000
-
-
3,971,962
3,971,962
-
-
The numbers of shares in the Company held during the financial year by each director and key management personnel
of Cellmid Limited, including their personally related parties, are set out below. There were no shares granted during the
reporting period as compensation.
Cellmid 2013 Annual Report 49
Notes to the Financial Statements
Continued
Balance at
Beginning
of the Year
Received
during the
Year on the
exercise of
options
Other
Changes
during the
Year
Balance at
the end of
the Year
2,725,250
22,500,000
1,875,000
-
-
-
-
-
-
-
-
-
-
-
-
4,024,750
6,750,000
-
-
-
22,500,000
1,875,000
-
5,155,700
5,155,700
-
-
-
-
-
-
Balance at
Beginning
of the Year
Received
during the
Year on the
exercise of
options
Other
Changes
during the
Year
Balance at
the end of
the Year
1,365,000
13,476,669
700,000
-
-
-
-
-
1,360,250
2,725,250
9,023,331
22,500,000
1,175,000
1,875,000
-
-
30 June 2013
Directors of Cellmid Limited
M Halasz
D King
R Beaumont
G Kaufman
M Rogers
Other key management personnel
J McGregor
N Falzon
A Bald
Maria Halasz owns 5,700,000 shares indirectly.
David King owns 22,500,000 shares indirectly.
Robin Beaumont owns 1,875,000 shares indirectly.
Martin Rogers owns 5,155,700 shares indirectly.
30 June 2012
Directors of Cellmid Limited
M Halasz
D King
R Beaumont
Other key management personnel
N Falzon
Maria Halasz owns 2,725,250 shares indirectly.
David King owns 22,500,000 shares indirectly.
Robin Beaumont owns 1,875,000 shares indirectly.
(iii) Other KMP Transactions
There have been no other transactions involving equity instruments other than those described in the tables above. The
chief executive officer is employed under an employment service contract.
50 Cellmid 2013 Annual Report
NOTE 7: AUDITOR’S REMUNERATION
During the year the following fees were paid or payable for services provided by the auditor of the parent entity, its related
practices and a non-related audit firm:
–
auditing or reviewing the financial statement BDO
– BDO Japan
NOTE 8: EARNINGS PER SHARE
a. Basic and diluted earnings per share:
Basic EPS and dilutive EPS
Consolidated Group
2013
$
54,900
10,200
65,100
2012
$
45,000
-
45,000
Consolidated Group
2013
$
2012
$
(0.27)
(0.46)
b.
Loss used in calculating basic and diluted earnings per share:
Loss
(1,541,307)
(1,972,483)
c. Weighted average number of shares used as the denominator
Weighted average number of ordinary shares used in calculating dilutive EPS
563,832,659
427,266,234
No.
No.
d.
Information concerning the classification of securities.
Options
Options granted to executives and directors are considered to be potential ordinary shares and have been included in
the determination of diluted earnings per share to the extent to which they are dilutive. In the year ended 30 June 2013,
these options were in fact anti-dilutive, and consequently diluted EPS is the same as basic EPS. The options have not
been included in the determination of basic earnings per share. Details relating to the options are set out in Note18.
Cellmid 2013 Annual Report 51
Notes to the Financial Statements
Continued
NOTE 9: CASH AND CASH EQUIVALENTS
Cash at bank and in hand
Consolidated Group
2013
$
2012
$
1,754,994
1,754,994
1,050,593
1,050,593
The effective interest rate on short term bank deposits was 3.5 - 4.5% (2012: 3.5-4.5%); these deposits were all on call.
Reconciliation of cash
Cash at the end of the financial year as shown in the statement of cash flows is reconciled to items in the statement of
financial position as follows:
Cash and cash equivalents
1,754,994
1,754,994
1,050,593
1,050,593
NOTE 10: TRADE AND OTHER RECEIVABLES
Trade receivables
Other receivables
Total current trade and other receivables
Effective interest rates and credit risk
Consolidated Group
2013
$
41,123
214,572
255,695
2012
$
52,791
18,377
71,168
The Group has no significant concentration of credit risk with respect to any single counterparty, or group of counterpar-
ties other than those receivables specifically provided for and mentioned within Note 10. The class of assets described as
‘trade and other receivables” is considered to be the main source of credit risk related to the group.
There is no interest rate risk for the balances of trade and other receivables.
There is no material credit risk associated with other receivables.
No receivables are past due or impaired.
52 Cellmid 2013 Annual Report
NOTE 11 : INVENTORIES
Inventory at lower of cost and net realisable value
Total inventories
NOTE 12: OTHER FINANCIAL ASSETS
Available-for-sale financial assets
Total non-current financial assets
Available-for-sale financial assets
Listed investments, at fair value:
– shares in listed corporations
Total available-for-sale financial assets
Consolidated Group
2013
$
2012
$
1,694,926
1,694,926
1,289,237
1,289,237
Consolidated Group
2013
$
-
-
-
-
2012
$
42,910
42,910
42,910
42,910
Cellmid 2013 Annual Report 53
Notes to the Financial Statements
Continued
NOTE 13: PLANT AND EQUIPMENT
Consolidated Group
Note
PLANT AND EQUIPMENT
Plant and equipment at cost:
Accumulated depreciation
Total plant and equipment
Note
Consolidated Group
Balance at 1 July 2011
Additions
Disposals
Depreciation expense
Balance at 30 June 2012
Additions through business combinations 28
Additions
Disposals
Depreciation expense
Balance at 30 June 2013
NOTE 14: INTANGIBLE ASSETS
Consolidated Group:
Balance at 1 July 2012:
Intangibles acquired with acquisition of Advangen Incorporated (Note 28)
Patent 1
Patent 2
Closing value at 30 June 2013
2013
$
366,065
(314,432)
51,633
Plant and
Equipment
$
11,764
31,931
-
(11,419)
32,276
9,257
26,734
-
(16,634)
51,633
2012
$
129,759
(97,483)
32,276
Total
$
11,764
31,931
-
(11,419)
32,276
9,257
26,734
-
(16,634)
51,633
Trademarks
& Licences
$
1,440
1,441,140
720,570
2,163,150
Intangible assets, other than goodwill, have finite useful lives. The Group has determined the useful life of the intangible
asset at 20 years.
There is no amortisation charge to the intangible assets in the 2013 financial year.
The net exchange difference regarding intangible assets acquired with the acquisition of Advangen Incorporated arising
on the translation of a foreign operation into the presentation currency is $152,805 (2012: Nil).
54 Cellmid 2013 Annual Report
NOTE 15: OTHER ASSETS
Prepayments
Total other assets
NOTE 16: TRADE AND OTHER PAYABLES
Unsecured liabilities:
Trade payables
Sundry payables and accrued expenses
Total trade and other payables
NOTE 17: PROVISIONS
Consolidated Group
Opening balance at 1 July 2012
Additional (Reversal of) provisions
Balance at 30 June 2013
Analysis of total provisions
Current
Non-current
Provision for Employee Benefits
Consolidated Group
2013
$
73,321
73,321
2012
$
30,638
30,638
Consolidated Group
2013
$
271,936
229,363
501,299
2012
$
112,702
145,875
258,577
Employee Benefits
Annual Leave
Long Service
Leave
$
$
135,448
(693)
134,755
34,753
17,755
52,508
Consolidated Group
2013
$
134,755
52,508
187,263
2012
$
135,448
34,753
170,201
A provision has been recognised for employee entitlements relating to annual leave and long service leave.
Cellmid 2013 Annual Report 55
Notes to the Financial Statements
Continued
NOTE 18: CONTRIBUTED EQUITY
Consolidated Group
Note
2013
No.
2012
No.
2013
$
2012
$
a. Share Capital
At the beginning of the year
520,843,117
392,634,129
20,741,843
18,780,723
Shares issued during the year
129,626,962
128,208,988
3,962,418
1,961,120
At the end of the year
18.c
650,470,079
520,843,117
24,704,261
20,741,843
b. Options
Balance at the beginning
of the year
Listed
Other
Directors
Executives
36,923,968
34,552,001
57,989
57,989
-
-
-
317,181,205
(6,599,995)
574,272
-
-
3,971,962
5,000,000
-
-
-
-
-
At the end of the year
18.d
354,105,173
36,923,968
632,261
57,989
Total contributed equity
25,336,522
20,799,832
Capital Risk Management
The consolidated entity’s objectives when managing capital are to safeguard its ability to continue as a going concern,
so that it can provide returns for shareholders and benefits for other stakeholders and to maintain an optimum capital
structure to reduce the cost of capital.
In order to maintain or adjust the capital structure, the consolidated entity may adjust the amount of dividends paid to
shareholders, return capital to shareholders, issue new shares or sell assets to reduce debt.
The consolidated entity would look to raise capital when an opportunity to invest in a business or company was seen as
value adding relative to the current parent entity’s share price at the time of the investment. The consolidated entity is not
actively pursuing additional investments in the short term as it continues to integrate and grow its existing businesses in
order to maximise synergies.
56 Cellmid 2013 Annual Report
c. Movement in ordinary share capital
Consolidated Group
Date
Details
Opening balance 1 July 2011
4/10/2011
Share issue
2/12/2011
Share issue
13/12/2011
Share issue
13/01/2012
Exercise of converting note options
24/01/2012
Share issue
17/02/2012
Exercise of converting note options
20/02/2012
Exercise of converting note options
27/02/2012
Exercise of converting note options
2/03/2012
Exercise of converting note options
16103/2012
Exercise of converting note options
28/03/2012
Exercise of converting note options
4/04/2012
Exercise of converting note options
12/04/2012
Exercise of converting note options
20/04/2012
Exercise of converting note options
4/05/2012
Share issue
7/05/2012
Share issue
30/05/2012
Share issue
12/06/2012
Share issue
Closing balance 30 June 2012
Opening balance 1 July 2012
27/07/2012
Share issue
31/08/2012
Capital raising costs
19/03/2013
Share issue
20/03/2013
Share issue
22/03/2013
Share issue
27/03/2013
Share issue
31/03/2013
Capital raising costs
9/04/2013
Capital raising costs
21/05/2013
Capital raising costs
Number of
shares
392,634,129
4,000,000
23,560,944
4,411,765
1,666,667
22,500
1,442,309
2,083,333
3,191,489
3,191,489
1,595,745
2,105,263
2,777,778
3,333,333
14,196,360
12,283,641
5,175,428
31,689,481
11,481,463
520,843,117
520,843,117
24,242,424
-
14,650,000
14,991,359
13,755,555
6,250,000
-
-
-
10/05/2013
Cellmid FPO escrowed for 3 months from Issue
7,500,000
20/05/2013
Cellmid FPO escrowed for 6 months from Issue
10,217,822
20/05/2013
Cellmid FPO escrowed for 12 months from Issue
38,019,802
Closing balance 30 June 2013
650,470,079
Issued price
$
0.0390
0.0170
0.0160
0.0120
-
0.0104
0.0096
0.0094
0.0094
0.0094
0.0095
0.0090
0.0090
0.0090
0.0165
0.0165
0.0165
0.0165
0.0165
0.0400
0.0400
0.0400
0.0400
0.0300
0.0300
0.0300
18,780,723
156,000
400,708
71,250
20,000
-
15,000
20,000
30,000
30,000
15,000
20,000
25,000
30,000
127,767
202,680
85,395
522,876
189,444
20,741,843
20,741,843
400,000
(20,000)
586,000
599,654
550,222
250,000
(7,014)
(60,000)
(8,573)
225,000
306,535
1,140,594
24,704,261
Cellmid 2013 Annual Report 57
Notes to the Financial Statements
Continued
Ordinary shares
No limit has been set on the total number of ordinary shares that the Company may issue. The ordinary shares do not
carry par value.
Ordinary shares entitle the holder to participate in dividends and the proceeds on winding up of the Company in propor-
tion to the number of and amounts paid on the shares held.
On a show of hand every holder of ordinary shares present at a meeting in person or by proxy, is entitled to one vote, and
upon a poll each share is entitled to one vote.
Consolidated Group
Number of
options
$
34,552,001
(549,995)
3,971,962
(6,050,000)
5,000,000
36,923,968
36,923,968
1,400,000
40,000
244,542,770
18,000,000
3,000,000
-
-
25,000,000
9,825,000
7,370,635
6,002,800
3,375,000
625,000
(2,000,000)
354,105,173
57,989
-
-
-
-
57,989
57,989
-
-
489,086
57,600
6,000
(22,908)
(32,705)
50,000
9,825
7,371
6,003
3,375
625
-
632,261
d. Movement in options
Date
Details
Opening balance 1 July 2011
8 Jan 12
Options lapsed
7 Mar 12
Options issued
8 May 12
Options lapsed
12 Jun 12
Options issued
Closing balance 30 June 2012
Opening balance 1 July 2012
14/08/2012
Options issued
15/08/2012
Options issued
29/10/2012
Options issued
30/10/2012
Options issued
16111/2012
Options issued
1/11/2012
Capital Raising Costs
1/12/2012
Capital Raising Costs
6112/2012
Options issues
19/03/2013
Options issues
20/03/2013
Options issues
22/03/2013
Options issues
27/03/2013
Options issues
2/04/2013
Options issues
16104/2013
Options lapsed
Closing balance 30 June 2013
58 Cellmid 2013 Annual Report
Options
On 14th and 15th August 2012, 1,440,000 share options were granted to Mr Darren Jones, Ms Anita Hicks and Ms Erin
Grant as part of the employee share scheme. The options are exercisable on or before 14th August 2017 with an exer-
cise price at $0.034 each. The options hold no voting or dividend rights and are not transferable.
On 30th October 2012, 18,000,000 share options were granted to Mr Martin Rogers in lieu of cash payment for consult-
ing fees accrued prior to his directorship with Cellmid. The options are exercisable on or before 23rd October 2016 with
an exercise price at $0.034 each. The options hold no voting or dividend rights and are not transferable.
These options vested immediately on grant date. Further details of these options are provided in the directors’ report.
The options hold no voting or dividend rights and are not listed. During the financial year, no other options vested with
key management personnel (2012: Nil).
Cellmid 2013 Annual Report 59
Notes to the Financial Statements
Continued
NOTE 19: RESERVES AND ACCUMULATED LOSSES
a. Reserves
Share based payment reserve
Balance 1 July
Option expense
Balance 30 June
Options
Consolidated Group
2013
$
2012
$
1,723,230
1,660,231
4,033
62,999
1,727,263
1,723,230
On 14th and 15th August 2012, 1,440,000 share options were granted to Mr Darren Jones, Ms Anita Hicks and Ms Erin
Grant as part of the employee share scheme. The options are exercisable on or before 14th August 2017 with an exer-
cise price at $0.034 each. The options hold no voting or dividend rights and are not transferable.
Available for sale reserve
Balance 1 July
Gain (loss) on revaluation
Reclassification impairment loss to profit and loss
Balance 30 June
General reserve
Balance 1 July
Net movement as a result of shams issued to minority interest
Contributions of equity
Balance 30 June
Foreign exchange reserve
Balance 1 July
Foreign exchange expense
Balance 30 June
-
-
-
-
-
22,855
-
22,855
-
22,855
-
216,257
216,257
10,120
(17,210)
(7,090)
7,090
-
-
33,860
33,860
(11,005)
22,855
-
-
-
Foreign exchange reserve is the net exchange difference arising on the translation of the financial statements into the
presentation currency and on the translation of a foreign operation into the presentation currency.
Total reserves
Balance 1 July
Revalution, option expense and foreign exchange expense
Balance 30 June
1,746,085
1,670,351
220,290
75,734
1,966,375
1,746,085
60 Cellmid 2013 Annual Report
b. Accumulated losses
Movements in accumulated losses were as follows:
Balance 1 July
Net income (loss) for the year
Balance 30 June
NOTE 20: CASH FLOW INFORMATION
a. Reconciliation of Cash Flow from Operations with Loss after Income Tax
Loss for the year
Non - cash flows in loss:
- Depreciation and amortisation
- Share base payment
- Bad and doubtful debt
- Gain on sale of financial asset
Consolidated Group
2013
$
2012
$
(20,441,455)
(18,471,095)
(1,528,041)
(1,970,360)
(21,969,496)
(20,441,455)
Consolidated Group
2013
$
2012
$
(1,541,307)
(1,972,483)
16,634
4,033
1,227
(48,875)
11,419
228,999
-
-
- Impairment loss on non - current investment
-
7,090
Changes in assets and liabilities, net of the effects of purchase of subsidiaries :
- (increase)/decrease in trade and other receivables
- (increase)/decrease in prepayments
- (increase)/decrease in inventories
- increase/(decrease) in trade and other payables
- increase/(decrease) in provisions
Cash flow from operations
22,890
(11,583)
(59,303)
146,453
17,063
(43,565)
617
(192,055)
124,873
76,836
(1,452,768)
(1,758,269)
Cellmid 2013 Annual Report 61
Notes to the Financial Statements
Continued
NOTE 21: CRITICAL ACCOUNTING ESTIMATES AND JUDGEMENTS
Estimates and judgements are continually evaluated and are based on historical experience and other factors, including
expectations of future events that may have a financial impact on the entity and that are believed to be reasonable under
the circumstances.
a. Critical accounting estimates and assumptions
The preparation of the financial statements requires management to make judgements, estimates and assumptions that
affect the reported amounts in the financial statements. Management continually evaluates its judgements and estimates
in relation to assets, liabilities, contingent liabilities, revenue and expenses. Management bases its judgements, estimates
and assumptions on historical experience and on other various factors, including expectations of future events, manage-
ment believes to be reasonable under the circumstances. The resulting accounting judgements and estimates will seldom
equal the related actual results. The judgements, estimates and assumptions that have a significant risk of causing a
material adjustment to the carrying amounts of assets and liabilities (refer to the respective notes) within the next financial
year are discussed below.
i. Estimated impairment of intellectual property
The group tests annually whether intellectual property has suffered any impairment, in accordance with the accounting
policy stated in note 1. The recoverable amounts of the intellectual property have been determined based on reviewing
the status of the research and development program, progress on its patent applications and projected cash flow calcu-
lations. These calculations require the use of assumptions, including estimating timing of cash flows, product develop-
ment and availability of resources to exploit the assets.
NOTE 22: EVENTS AFTER THE REPORTING PERIOD
There are two items which have occured after the reporting date as follows:
- Pacific Edge have issued 1,084,622 shares to Cellmid having achieved their requisite milestone. The shares have been
issued pursuant to the midkine diagnostic licence agreement signed on 17 May 2010; and
- The escrow shares issued during the year will be released within the next 12 months;
Other than these items, no other matter or circumstance has arisen since 30 June 2013 that has significantly affected,
or may significantly affect the Group’s operations, the results of those operations, or the Group’s state of affairs in future
financial years.
NOTE 23: RELATED PARTY TRANSACTIONS
Related Parties
a. The group’s main related parties are as follows:
Parent entities:
Cellmid Limited is the ultimate parent entity.
Subsidiaries:
For details of disclosures relating to subsidiaries, refer to Note 25: Controlled Entity.
Key management personnel:
For details of disclosures relating to key management personnel, refer to Note 6: Interests of Key Management
Personnel (KMP) and the remuneration report in the directors’ report.
62 Cellmid 2013 Annual Report
b. Transactions with related parties
Key management personnel:
Martin Rogers received 18,000,000 options in lieu of a consulting fee. The consulting work was performed prior to his
directorship.
There were no other related party transactions during the year ended 30 June 2013.
Subsidiaries:
The transactions with subsidiaries have been eliminated on consolidation of the group.
NOTE 24: FINANCIAL RISK MANAGEMENT
Specific Financial Risk Exposures and Management
The Group’s activities expose it to a number of financial risks as described below. The Group’s overall risk management
program seeks to minimise potential adverse effects on the financial performance of the Group. To date, the group has
not had the need to utilise derivative financial instruments such as foreign exchange contracts or interest rate swaps to
manage any risk exposures identified.
The totals for each category of financial instruments, measured in accordance with AASB 139 as detailed in the account-
ing policies to these financial statements, are as follows:
Financial assets
Cash and cash equivalents
Loans and receivables
Available-for-sale financial assets
Total financial assets
Financial liabilities
Financial liabilities at amortised cost:
- trade and other payables
Total financial liabilities
a. Credit risk
Note
Consolidated Group
2013
$
2012
$
1,754,994
1,050,593
255,695
-
71,168
42,910
2,010,689
1,164,671
501,299
501,299
258,577
258,577
9
10
12
16
Credit risk is managed on a Group basis. The group has no significant concentration of credit risk.
The maximum exposure to credit risk by class of recognised financial assets at the end of the reporting period is
equivalent to the carrying value and classification of those financial assets (net of any provisions) as presented in the
table above.
Trade and other receivables that are neither past due nor impaired are considered to be of high credit quality.
Credit risk related to balances with banks and other financial institutions is managed by management in accord-
ance with approved board policy. Such policy requires that surplus funds are only invested with counterparties with a
Standard & Poor’s rating of at least AA-.
Cellmid 2013 Annual Report 63
Notes to the Financial Statements
Continued
b. Liquidity risk
The Group manages this risk through the following mechanisms:
- preparing forward-looking cash flow analysis in relation to its operational, investing and financing activities;
- managing credit risk related to financial assets;
- only investing surplus cash with major financial institutions The Group is not exposed to any material liquidity risk.
The table below analyse the group’s financial liabilities into relevant maturity groupings based on their contractual
maturities for:
(a) all non-derivative financial liabilities
(b) net and gross settled derivative financial instruments for which the contractual maturities are essential for an
understanding of the timing of the cash flows.
The amounts disclosed in the table are the contractual undiscounted cash flows. Balances due within 12 months equal
their carving balances as the impact of discounting is not significant.
Contractual
maturities of
financial liabilities
Less than
6 months
6-12
months
Between
1 and 2
years
Between
2 and 5
years
Over 5
years
Total
contractual
cash flow
Carrying
amount
liabilities
As 30 June 2013
$
$
$
$
$
$
$
Non-derivative
Trade and other
payable
Total
Derivative
Borrowings
Total
501,299
501,299
-
-
Contractual
maturities of
financial liabilities
Less than
6 months
6-12
months
As 30 June 2012
$
$
Non-derivative
Trade payable
Total
Derivative
Borrowings
Total
258,577
258,577
-
-
c. Market risk
Foreign exchange risk
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
501,299
501,299
-
-
Between
1 and 2
years
Between
2 and 5
years
Over 5
years
Total
contractual
cash flow
Carrying
amount
liabilities
$
$
$
$
$
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
258,577
258,577
-
-
Exposure to foreign exchange risk may result in the fair value or future cash flows of a financial instrument fluctuating
due to movement in foreign exchange rates of currencies in which the Group holds financial instruments which are
other than the AUD functional currency of the Group.
64 Cellmid 2013 Annual Report
The Group has no significant concentration of foreign exchange risk. The maximum exposure to foreign exchange risk
is the fluctuation in the US dollar on its USD denominated bank account and also the Japanese Yen bank accounts.
Price risk
The Group is not exposed to any material price risk.
NOTE 25: SUBSIDIARY AND TRANSACTIONS WITH NON-CONTROLLING INTEREST
a. Significant investments in subsidiary
Country of Incorporation
Percentage Owned (%)
Subsidiaries of Cellmid Limited
Advangen International Pty Limited
Advangen Limited
Advangen Incorporated
Australia
Australia
Japan
2013
2012
95
100
100
95
-
-
NOTE 26: SEGMENT INFORMATION
Identification of reporting segments
The Group’s organised into two operating segments: (1) research and development of diagnostics and therapeutics and
(2) research, development and marketing of hair growth products. These operating segments are based on the internal
reports that are reviewed and used by the Board of Directors (identified as the Chief Operating Decision Makers (CODM))
in assessing performance and in determining the allocation of resources. There is no aggregation of operating segments.
The CODM reviews both adjusted earnings before interest, tax, depreciation and amortisation (segment result) and profit
before income tax.
Types of products and services
The principal products and services of each of these operating segments are as follows:
R&D
R&D and marketing
Diagnostics and therapeutics for cancer and inflammatory conditions
Hair growth products
Geographic segment information
The primary geographic segment within which the Group operates is Australia as at 30 June 2013. For primary reporting
purposes, the Group operates in two geographic segment as described as at 30 June 2013.
Major customers
During the year ended 30 June 2013 approximately 70% of the Group’s external revenue was derived from sales to Frost-
bland Pty Ltd (32%) and Fujikura Kasai Co Limited (38%) through the biotechnology and retailing operating segments.
Cellmid 2013 Annual Report 65
Notes to the Financial Statements
Continued
Operating segment information
30 June 2013
Biotechnology
Retailing
Retailing
Consolidated
Revenue
Sales revenue
Total sales revenue
Interest received
Royalties
Rental revenue
Government grant received
Other revenue
Total Revenue
Expenses
Share-based compensation
Gain on disposal of financial assets
Depreciation
Finance costs
$
$
Australia
Australia
215,279
215,279
30,833
358
24,000
115,167
-
385,637
311,098
311,098
-
-
-
-
398
311,496
$
Japan
15,272
15,272
-
-
-
-
8
15,280
$
541,649
541,649
30,833
358
24,000
115,167
406
712,413
(2,374,994)
(576,661)
(115,015)
(3,066,671)
(4,032)
48,875
(13,919)
(1,110)
-
-
(156)
(14)
-
-
(2,561)
-
(4,032)
48,875
(16,635)
(1,124)
Loss before income tax expenses
(1,959,543)
(265,335)
(102,296)
(2,327,173)
Income tax benefit
Loss after income tax benefit
785,866
(1,541,307)
30 June 2013
Biotechnology
Retailing
Retailing
Consolidated
$
$
Australia
Australia
$
Japan
$
2,545,805
369,363
3,078,552
5,993,720
(532,592)
(79,483)
(76,487)
-
-
5,993,720
(688,562)
(688,562)
Assets
Segment assets
Unallocated assets:
Other financial assets
Total assets
Liabilities
Segment liabilities
Total liabilities
66 Cellmid 2013 Annual Report
30 June 2012
Biotechnology
Retailing
Retailing
Consolidated
$
$
Australia
Australia
$
Japan
$
Revenue
Sales of products
Total sales revenue
Interest received
Royalties
Rental revenue
Government grant received
Other revenue
Total Revenue
Expenses
Share-based compensation
Gain on disposal of financial assets
Depreciation
Finance costs
12,590
12,590
5,370
704
24,000
-
11,077
53,741
115,704
115,704
-
-
-
-
1,828
117,532
(2,412,460)
(236,921)
(228,999)
49,237
(11,110)
(39,509)
-
-
(309)
(205)
Loss before income tax expenses
(2,589,100)
(119,903)
Income tax benefit
Loss after income tax benefit
Assets
Segment assets
Unallocated assets:
Other financial assets
Total assets
Liabilities
Segment liabilities
Total liabilities
2,135,203
340,149
(415,667)
(13,111)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
736,520
-
-
42,910
128,294
128,294
5,370
704
24,000
-
12,905
171,273
(2,649,381)
(228,999)
49,237
(11,419)
(39,714)
(2,709,003)
(1,972,483)
2,475,352
2,518,262
(428,778)
(428,778)
Cellmid 2013 Annual Report 67
Notes to the Financial Statements
Continued
NOTE 27: COMMITMENTS
Lease commitments - operating
Committed at the reporting date but not recognised as liabilities, payable:
Within one year
One to five years
More than five years
Consolidated Group
2013
$
174,039
554,061
728,100
2012
$
-
-
-
Operating lease commitments includes contracted amounts for office space under non-cancellable operating lease expir-
ing within five years with no option to extend.
NOTE 28: BUSINESS COMBINATIONS
On 24 May 2013 Cellmid Limited acquired 100% of the ordinary shares of Advangen Incorporated (Japanese entity) for
the total consideration transferred of JPY¥285,171,564. This has been translated to AUD$2,893,968 using the exchange
rate per Reserve Bank of Australia (RBA) on 24 May 2013. The acquired business contributed revenues of $15,280 and
loss after tax of $102,297 to the Group for the period from 25 May 2013 to 30 June 2013. The values identified in relation
to the acquisition of Advangen Incorporated are final as at 30 June 2013.
Details of the acquisition are as follows:
Book Value
Fair Value Exchange Rate
Fair Value
¥JPY
¥JPY
41,182,636
41,182,636
19,594,272
19,594,272
31,742,886
31,742,886
2,850,035
2,850,035
848,292
848,292
-
198,099,144
(9,145,701)
(9,145,701)
87,072,420
285,171,564
-
-
285,171,564
98.54
98.54
98.54
98.54
98.54
98.54
98.54
Cash and cash equivalents
Trade and other receivables
Inventories
Other assets
Plant and equipment
Intangibles assets
Trade and other payables
Net assets acquired
Goodwill
Acquisition date fair value of the total consideration
transferred
Representing:
- Cash
- Fair value of issued shares
Cash used to acquire business, net of cash acquired:
Cash to acquire subsidiary
Less: Cash and cash equivalents on acquisition
Net cash used
68 Cellmid 2013 Annual Report
$AU
417,928
198,846
322,132
28,923
8,609
2,010,342
(92,812)
2,893,968
-
2,893,968
1,221,839
1,672,129
2,893,968
1,221,839
417,928
803,911
NOTE 29: CONTIGENT LIABILITIES
a.
b.
Contingent liabilities
The parent entity and Group had no contingent liabilities at 30 June 2012 or at 30 June 2013.
Contingent assets
The parent entity and Group had no contingent assets at 30 June 2012 or at 30 June 2013.
NOTE 30: COMPANY DETAILS
The registered office of the company is:
Suite 1802, Level 18,
15 Castlereagh Street Sydney NSW 2000
The principal places of business are:
Cellmid Limited,
Suite 1802, Level 18,
15 Castlereagh Street Sydney NSW 2000
Advangen International Pty Limited.
Suite 1802, Level 18,
15 Castlereagh Street Sydney NSW 2000
Advangen Limited.
Suite 1802, Level 18,
15 Castlereagh Street Sydney NSW 2000
Advangen Incorporated,
Chiba Industry Advancement Centre Tokatsu Techno Plaza
511-6 Kashiwanoha Kashiwa,
Chiba 277-0082 Japan
Cellmid 2013 Annual Report 69
Directors’
Declaration
DIRECTORS’ DECLARATION
The directors of the company declare that:
1. the financial statements and notes, as set out on pages 31-69, are in accordance with the Corporations Act 2001, the
Corporations Regulations 2001 and other mandatory professional reporting equirements and:
a. comply with Accounting Standards, which, as stated in accounting policy Note 1 to the financial statements,
constitutes explicit and unreserved compliance with International Financial Reporting Standards (IFRS); and
b. give a true and fair view of the financial position as at 30 June 2013 and of the performance for the year ended on
that date of the company and the group;
c. the remuneration disclosures contained in the Remuneration Report comply with section 300A of the Corporations
Act 2001;
2. the Chief Executive Officer and Chief Financial Officer have each declared that:
a. the financial records of the company for the financial year have been properly maintained in accordance with s 286
of the Corporations Act 2001;
b. the financial statements and notes for the financial year comply with Accounting Standards; and
c. the financial statements and notes for the financial year give a true and fair view; and
3. in the directors’ opinion there are reasonable grounds to believe that the group will be able to pay its debts as and when
they become due and payable.
Signed in accordance with a resolution of the Board of Directors made pursuant to Section 295 (5) of the Corporations
Act 2001.
Dr David King
Director
Dated 28th day of August 2013
70 Cellmid 2013 Annual Report
Cellmid 2013 Annual Report 71
72 Cellmid 2013 Annual Report
Additional
Information
The information in this section has been prepared as at 12 September 2013.
20 LARGEST SHAREHOLDERS
Holder Name
Cell Signals Inc
Seistend (Super) Pty Ltd
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