212021
ANNUAL
REPORT
01
CORPORATE
DIRECTORY
CORPORATE DIRECTORY
DIRECTORS
Brett Mitchell
Executive Chairman
Nativ Segev
Non-Executive Director
Stephen Parker
Senior Independent Director and Chairman of the Corporate
Governance Committees
COMPANY SECRETARY
David Lim
Rachel Kerr
Roby Zomer
Managing Director and CEO
Ross Walker
Non-Executive Director
Evan Hayes
Non-Executive Director
REGISTERED OFFICE AND PRINCIPAL PLACE OF BUSINESS
1202 Hay Street
West Perth WA 6005
Tel: +61 8 6382 3390
SOLICITORS
Steinepreis Paganin
Level 4, The Read Buildings
16 Milligan Street
Perth WA 6000
AUDITORS
Ernst & Young
EY Building
11 Mounts Bay Road
Perth WA 6000
SECURITIES EXCHANGE LISTING
MGC Pharmaceuticals Ltd securities are listed on the Australian Securities Exchange (ASX) and the London Stock
Exchange (LSE).
ASX Code: MXC
LSE Code: MXC
SHARE REGISTRY
Computershare Investor Services Pty Limited
Level 11
172 St Georges Terrace
Perth WA 6000
WEBSITE
www.mgcpharma.com.au
2
02
CONTENTS
CONTENTS
CORPORATE DIRECTORY
MANAGING DIRECTOR’S LETTER TO SHAREHOLDERS – COMPANY ACTIVITIES
2021 FINANCIAL YEAR HIGHLIGHTS
DIRECTORS’ REPORT
AUDITOR’S INDEPENDENCE DECLARATION
CONSOLIDATED STATEMENT 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 TO MEMBERS
ADDITIONAL ASX INFORMATION
2
4
6
8
29
30
31
32
33
34
67
68
73
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03
MANAGING DIRECTOR’S
LETTER TO
SHAREHOLDERS
MANAGING DIRECTOR’S
LETTER TO SHAREHOLDERS –
COMPANY ACTIVITIES
Dear shareholders,
It scarcely needs to be said that the past year has
proved challenging for many across the globe, given the
continuing impact of COVID-19. I am pleased and proud of
our company and our progress, and of the MGC Pharma
team who have worked to make this possible. We have
continued to build our global strategy and expand our
operations, maintaining our integral “Plant to Medicine”
ethos. Our research and development of the MGC Pharma
products, and the partnerships we have cemented over the
past year mean that we are in a strong position to continue
to expand our commercial strategy and positive growth
trajectory capitalising on immediate market concerns and
opportunities.
We have continued to make excellent progress in
commercialising our proprietary Phytocannabinoid medicines
and treatments, which are now available to patients on a global
scale as we carry out secondary and tertiary clinical trials in
pharmaceutical jurisdictions.
During 2021, MGC Pharma had prescribed 12,457 units
representing a 247% increase on last years sales. This clearly
demonstrates the increasing demand for effective, high quality
Phytocannabinoid medicines.
Our research and development programme, which spans
global markets and pharmaceutical jurisdictions have delivered
material progress in the timeline to delivery. Over the course
of this year, we have advanced clinical trials on our three key
products: CimetrA™, CogniCann® and CannEpil, and have
conducted studies on the efficacy of cannabinoid formulations
in the development of treatment for glioblastoma, delivering
significant results.
Our proprietary non-phytocannabinoid treatment, ArtemiC™,
designed for the alleviation of the symptoms of COVID 19, has
undergone a phase II clinical trial at hospitals in Israel and in
India, meeting all safety and efficacy targets. The treatment
has since been approved as an IMP and has been registered
for a patent application submitted to the Slovenian Intellectual
Property Office under the new name CimetrA™. A phase III
clinical trial for the CimetrA treatment is currently ongoing at
Rambam Health Care Campus and Nazareth Hospital EMMS
in Israel. The construction of our production facility has
commenced in Malta following a cash grant of $4.8m and is
due for completion in Q4 of this year; once fully operational,
the facility will manufacture CimetrA™, in addition to other MGC
Pharma liquid dose medicines. Further to this, and following the
year end, in August we received approval to import CimetrA™
into India for emergency Use authorisation registration. These
are all hugely positive steps on the way to full scale production
and distribution, and the alleviation of the symptoms of
COVID-19 in patients across the globe.
The company received ethics committee approval for Phase
IIb clinical trial for CannEpil® a cannabinoid-based drug for the
treatment of refractory (or drug resistant) epilepsy. The trial will
be carried out at hospitals in Israel, and the drug has now been
added to the Primary Care Reimbursement service in Ireland
under the Medical Cannabis Access Programme, of which we
are proud to be part.
Further R&D includes the phase II clinical trial at University of
Notre Dame in Perth for CogniCann®, which treats the effects of
dementia and Alzheimer’s, and a botanical research partnership
with the Royal Melbourne Institute of Technology.
We have cemented several key relationships over the course
of the year which will enable the broader distribution and
patient access to MGC Pharma products – including signing
4
A TRANSFORMATIONAL YEAR FOR MGC PHARMA,
CEMENTING OUR POSITION AS A PLANT BASED
BIO-PHARAMA COMPANY
agreements with LYPHE Group for the prescription and
dispensation of the Mercury Pharma product range in the UK,
and with Swiss PharmaCan AG for the distribution of ArtemiC™
Rescue. MGC Pharma has now appointed IM Cannabis Corp
as the exclusive importer of CannEpil to Israel. Post year end,
in August, we announced a binding US$24 million supply and
distribution agreement with AMC Holdings, which will introduce
MGC Pharma products to the US, the largest pharmaceutical
market in the world.
Our listing on the London Stock Exchange was a historic
moment for the company as MGC Pharma became the first
medicinal cannabis company quoted on the exchange, this
followed a £6.5m placement. Our dual listing now reflects our
global reach and capacity and has served to bring wider investor
attention to our company as we continue to develop and refine
our products and company offering. The funds raised at IPO
complement a $15m convertible securities financing agreement
with Mercer Street Global – which have allowed us to fully
accelerate our research, trial and production workstreams over
the course of the year.
I’d like to take the opportunity on behalf of the board to thank
our employees for their hard work, and our customers and loyal
shareholders for their continued support, without which the
progress of the company would not be possible. I look forward
to updating shareholders on our developments as we continue
to grow operationally and commercially.
Yours Sincerely,
Roby Zomer
CEO & Managing Director
5
04
2021 FINANCIAL
YEAR HIGHLIGHTS
2021 FINANCIAL
YEAR HIGHLIGHTS
6
AS AT 30 JUNE 2021
12,547 27,164
PHYTOCANNABINOID UNIT SALES
SUPPLEMENT PRODUCT SALES
LSE
LISTING
CLINICAL
RESEARCH
ORGANISATION
Successfully completed a £6.5million placement to
become the first medicinal cannabis company to list on
the London Stock Exchange.
Acquired 100% of MediCaNL, an Israeli company operating
in, and providing specialist services to the pharmaceutical
sector for the development of new medicines.
ETHICS
COMMITTEE
APPROVED
CLINICAL RESEARCH
RESULTS
Received from Schneider Children’s Medical Centre of
Israel for MGC Pharma’s proprietary epilepsy treatment,
CannEpil® to commence a Phase IIb Clinical Trial.
Results from its Phase II clinical and preclinical studies
support ArtemiC™ being effective for addressing cytokine
over production in all tested COVID-19 patients.
CannEpil®
PATENT
ACCEPTED
Added to the Primary Care Reimbursement Service in
the Republic of Ireland making it free of charge for Irish
patients prescribed the treatment under its Medical
Cannabis Access Program.
Patent application for CimetrA™, the Investigational
Medicinal Product assigned to MGC Pharma, has been
accepted by the Slovenian Intellectual Property Office.
7
05
DIRECTORS’
REPORT
DIRECTORS’
REPORT
8
The Directors present their report on MGC Pharmaceuticals Ltd (“the Company” or “the Parent”) and its controlled entities
(collectively, “MGC”, “the Group” or “MGC Pharma”) for the financial year ended 30 June 2021.
DIRECTORS
The names of Directors in office at any time during or since the end of the year are:
DIRECTOR
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayes
TITLE
Executive Chairman
Managing Director & CEO
Non-Executive Director
Non-Executive Director
Non-Executive Director
Non-Executive Director
APPOINTMENT
DATE
4 April 2013
15 February 2016
15 February 2016
15 February 2016
13 March 2019
1 September 2020
RESIGNATION
DATE
-
-
-
-
-
-
Directors were in office for the entire year and up to the date of this report unless otherwise indicated.
COMPANY SECRETARY
Rachel Kerr held the position of Company Secretary for the full financial year. Narelle Warren and Nadine Barry both
assisted in the position during the year to assist in cover for Rachel whilst on maternity leave, until a full-time replacement
was found in David Lim who was appointed on 3 June 2021.
PRINCIPAL ACTIVITIES
MGC Pharma (ASX/LSE: MXC) is a European based bio-pharma company trading on both the Australian Securities
Exchange and the London Stock Exchange, specialising in the development and supply of standardised phytomedicines
to patients globally. It has three key clinical projects today, as well as a pipeline of further potential therapies: CimetrA,
a Phase 3 symptomatic treatment for early COVID-19, CannEpil, a Phase 2b cannabis-based therapy for drug-resistant
Epilepsy, and CogniCann, in a Phase 2 trial for symptomatic relief of Dementia. The Company currently generates
revenues from its ArtemiC range of products, and its cannabinoid products primarily distributed within Australia, the UK,
and South America.
MGC Pharma is focused on the production of pharmaceutical grade phytomedicine products supported by ongoing
research and development activities, as well as the production of Active Pharmaceutical Ingredient (API) of various
cannabinoids, driven through a fully vertically integrated product development pipeline.
OPERATING RESULTS
The consolidated loss of the Group from continuing operations amounted to $15,409,341 (2020: $18,769,799).
DIVIDENDS PAID OR RECOMMENDED
No dividends have been paid or declared for payment during, or since, the end of the financial year.
9
REVIEW OF OPERATIONS
HIGHLIGHTS
Clinical Research & Development Programs
During the year the Company has successfully demonstrated MGC Pharma’s nature to pharma pipeline and clinical
capabilities with a non-phytocannabinoid product, that strategically adds a new dimension of development and revenue to
MGC Pharma’s future. With CimetrA™, MGC Pharma has rapidly moved a new product to the forefront of the Company’s
clinical pipeline based on a global market need, with several benefits to the Company: new territories for distribution
previously off-limits, deeper engagement with doctors and the pharma industry at large, larger scope of possible
formulations and a significant market segment in which to be a first mover.
Additionally, MGC Pharma has continued its work on developing a robust pre-clinical pipeline to ensure a lasting continuity
of products reaching Central Market Authorisation, providing the Company with a longstanding footing in the emerging
plant-based biopharma industry.
With the Company poised to bring three products to Central Market Authorisation over the next three years, the Company
is fulfilling its vision of becoming a leader in the emerging phytopharma sector which has been its focus for the past
six years, as well as significantly expanding the footprint of its clinical engagement and potential geographic market
segment.
These achievements have been powered by:
■ Completion of a Phase II Clinical Trial for MGC Pharma’s anti-inflammatory product, ArtemiC™, results of which were
announced in December 2020. The Clinical Trial delivered excellent results by meeting all primary and secondary
endpoints, demonstrating a full safety profile with no drug related adverse events
■ Recruitment of patients into the CimetrA™ Phase III clinical trial commenced at Rambam Health Care Campus and
Nazareth Hospital EMMS in Israel in June 2021
■ Following research into the treatment of glioblastoma showing MGC Pharma’s proprietary formulation, CBG, impairs
the major hallmarks of glioblastoma progression, commencement of the study into the use of SNEDDS nano
technology for the treatment of aggressive glioblastoma brain cancer
■ Ethics committee approval from Schneider Children’s Medical Centre of Israel for MGC Pharma’s proprietary epilepsy
treatment, CannEpil® to commence a Phase IIb Clinical Trial
■ Enrolment of patients at the University of Notre Dame in Perth, Western Australia for MGC Pharma’s CogniCann®
phase II Clinical Trial on patients with Dementia and Alzheimer’s disease
Global Pharma Operations
MGC Pharma has greatly expanded its ability to sell (and manufacture) its phytocannabinoid products over 2021,
operating in Australia, Brazil, UK, and Ireland, as a result of long-term regulatory contact and finding local distributors able
to provide MGC Pharma products to patients. With the onboarding of a global sales officer and a sales team in Australia,
MGC Pharma’s sales are growing month by month, and with the addition of new products such as flowers and ArtemiC™,
the company is moving towards break even (not including Clinical Trials).
Key highlights during the year relating to pharma operations:
■ Record cumulative sales of phytocannabinoid products in FY 21, with 12,457 units sold worldwide, amounting to
~$2.0million in revenues
■ €3.1million ($4.9million) government grant secured from Malta Enterprise with construction underway for a fully
certified Good Manufacturing Practice (GMP) facility in Malta, for the production of ArtemiC™
■ CannEpil® has been added to the Primary Care Reimbursement Service in the Republic of Ireland making it free of
charge for Irish patients prescribed the treatment under its Medical Cannabis Access Program
10
Key Licences, Approvals and Distributions Agreements
■ Agreements signed with IM Cannabis Corp for the distribution of CannEpil® in Israel.
■ Master supply and distribution agreement secured with leading European nutraceuticals producer and distributor,
Swiss PharmaCan AG for a minimum of 40,000 units of ArtemiC™ Rescue per quarter of which the first two batches
have been delivered
■ Landmark UK import permit granted in September 2021 for MGC Pharma’s CannEpil+, designed to treat Refractory
Epilepsy
■ Subsequent to year end, the Company executed a US$24 million supply agreement with AMC Holdings Inc of MGC
phytomedicine products over three years, with a minimum of US$3 million within the first year, subject to the grant of a
National Clinical Trial Number
Corporate
■ MGC Pharma becomes the first medicinal cannabis company to list on the London Stock Exchange following
a £6.5 million (~A$12m) Placement, strongly supported by UK funds
■ MGC Pharma delivered a breakout result with its strong revenue growth in its phytocannabinoid product sales during
the year, generating $2.726m in FY21 against $1.197m in FY20 (increase of 130%)
■ Acquisition of Medicinal Cannabis Clinics completed, enabling distribution that provides stronger sales with
significantly higher profit margins while maintaining competitive product prices
■ Acquisition of global pharmaceutical clinical research company, MediCaNL, to deliver MGC Pharma significant cost
synergies and expedited clinical trial processes
RESEARCH AND DEVELOPMENT / CLINICAL TRIALS
Phase II ArtemiC™ Clinical Trial
During the year MGC Pharma released further results from its Phase II clinical and preclinical studies on ArtemiC™, which
support ArtemiC™ being effective for addressing cytokine over production in all tested COVID-19 patients. The Preclinical
Trial was performed in the SIA preclinical Lab (Good Laboratory Practice (GLP) certified) in Israel. The ARDC model is the
recommended preclinical animal model for Cytokine Storm, for the prediction of the human model of COVID-19 patients.
The trial delivered strong results across a full safety profile with no drug-related adverse effects and is an immensely
positive result for the treatment of COVID-19 globally.
Recruitment of patients into the CimetrA™ Phase III clinical trial
MGC Pharma received Ethics Committee approvals from Rambam Health Care Campus, Haifa and Nazareth Hospital
EMMS in Israel and began data collection under the Phase III clinical trial to evaluate the efficacy and safety of ArtemiC™
as a treatment for moderate hospitalised patients diagnosed with COVID-19, and to provide additional data for claims on
the product as an Investigational Medicinal Product (IMP).
As part of the Phase III clinical trial, the classification of the product has changed from a food supplement to an IMP.
As a result, the product name under the trial has changed from ArtemiC™ to CimetrA™. CimetrA™ becoming an IMP will
include changing the drug carrier to a new polymeric drug carrier GraftBio™ (SNEDD – Self Nano Drug Delivery), with a
view to potentially being registered as a drug in the future. The trial will ultimately enrol a total of 252 patients and will be
conducted over a 28-day period. The company is confident that the clinical trial will show CimetrA™ to be an effective
treatment against the symptoms of COVID-19.
Successful research results into cannabinoid treatment of glioblastoma
Working in collaboration with the Slovenian National Institute of Biology and Neurosurgery Department at the University
Medical Centre, MGC Pharma has expanded the research program on the use of cannabinoids in the treatment
of aggressive Glioblastoma brain cancer to include testing the effect of both MGC Pharma proprietary treatments
Cannabidiol (‘CBD’) and Cannabigerol (‘CBG’) following successful clinical trial results.
The results from 18 patient tumour samples show for the first time that the Company’s proprietary formulation, CBG,
exerts a superior effect in impairing the major hallmarks of Glioblastoma progression, i.e., fast proliferation and invasion,
and particularly enhancing Glioblastoma cell death. CBG has shown it can destroy therapy-resistant Glioblastoma stem
cells, which are the root of cancer development and extremely resistant to various treatments of this lethal cancer.
The expanded In-vitro cannabinoid study on Glioblastoma treatment is focused on testing cannabinoid formulations on
fresh glioblastoma tumour tissues, obtained from patients after surgical removal of the tumour to determine the optimal
cannabinoid preparation for the effective treatment of the remaining cancer. The aim of this research is to develop
novel formulations and define the clinical protocols for clinical trials for the treatment of high-grade brain tumours with
cannabinoids.
11
Ethics Committee approval for Phase IIb clinical trial for CannEpil®
In May 2021, MGC Pharma announced the receipt of Ethics Committee approval for its Phase IIb randomised, double
blind, placebo controlled clinical study for CannEpil®, a phytocannabinoid derived IMP, designed to treat Drug Resistant
Epilepsy with a high CBD, low THC formula. The Clinical Trial for CannEpil® will take place at the Schneider Children’s
Medical Hospital in Israel and will focus on the safety and efficacy of CannEpil® as an add-on treatment for children and
adolescents with treatment resistant epilepsy, also known as Refractory Epilepsy. The trial is targeting the recruitment of
more than 100 patients which began in July. This trial involves healthy volunteers and aims to demonstrate the safety of
CannEpil® in order to provide supportive data to the regulatory authorities.
Enrolment of patients for CogniCann® Phase II clinical trial
CogniCann®, a formulation of phytocannabinoids that has been developed with the specific aim of treating Alzheimer’s
and Dementia, is undergoing a Phase II clinical trial at the University of Notre Dame in Perth, Western Australia with 21
patients currently enrolled as of 25 May 2021. The Trial is designed to evaluate the potential behavioural benefits
of CogniCann® on patients with Dementia and Alzheimer’s disease. The randomised double blind, crossover,
placebo-controlled Clinical Trial will enrol 50 patients over its duration and is expected to last until Q4 2021.
PHARMA OPERATIONS
Breakout year delivered on phytocannabinoid product sales growth in FY21
Throughout FY21, MGC Pharma delivered a breakout result with its strong revenue growth in its phytocannabinoid
product sales during the year, generating $2.726m in FY21 against $1.197m in FY20 (increase of 130%). This was
complemented with a significant reduction in production costs from the previous year, with cost of goods sold (COGS)
reduced significantly as a result of improved production efficiencies on increased volumes. As at the end of 30 June 2021,
the Company had sold a total of 12,457 prescribed units of its standardised affordable cannabinoid medicines across
Australia, UK & Brazil, a record for the Company.
Additionally, post the financial year end, MGC Pharma has implemented new commercial initiatives which are aimed
at enhancing sales growth in the Company’s key Australian market. These include entering a Contract Sales Team
Agreement with A. Menarini Australia Pty Ltd. (Menarini), the Australian arm of global pharmaceutical company, Menarini
Group, who will provide eight additional sales personnel to the team and the launch of a new form factor, MGC THC 20
whole flower.
12 Month Cumulative Phytocannabinoid Product Sales to June 2021
Units
14,000
12,000
10,000
8,000
6,000
4,000
2,000
0
Jul-20
Aug-20
S ep-20
Oct-20 Nov-20 Dec-20
Jan-21 Feb-21 Mar-21
A pr-21 M ay-21
Jun-21
Cumulative sales
Monthly sales
Cumulative units
$A
$2,000,000
$1,800,000
$1,600,000
$1,400,000
$1,200,000
$1,000,000
$800,000
$600,000
$400,000
$200,000
$0
12
MGC Pharma expects to see strong revenue growth of its phytocannabinoid products in the coming months on the back
of these commercial changes, particularly within the Australian market.
Phytocannabinoid Sales by Product for the FY21
High CBD 54.17%
(MP100, MP1:30 and CannEpil)
High THC 11.13%
(MP7:1, MP15:1 and MP25T)
Balanced 34.70%
(MP1:1 & CogniCann)
Maltese GMP facility construction completion on schedule for October 2021
In Q2 FY 21, the Company was awarded a ~$4.95million (€3.1million) grant from Malta Enterprise to renovate and extend
the Company’s existing Clinical Research Organisation facility in Malta to include a fully functioning GMP certified
manufacturing facility for ArtemiC™. Building work commenced in December 2020, and has made good progress, with
construction expected to be completed in October 2021. The production equipment fit out and commissioning of the
Malta facility to full operational capacity will be completed in 2022.
The facility will enable the Company to immediately increase ArtemiC™ production volumes and reduce logistics costs via
the Malta facility due to its optimal geographic location and shipping access.
Main entrance
Production corridor
CannEpil® made available for patients in Ireland
MGC Pharma’s proprietary cannabis derived epilepsy Investigational Medicinal Product (IMP) CannEpil® was added to
the Republic of Ireland’s Health Service Executive (HSE) following the incorporation of the Medical Cannabis Access
Programme (MCAP) into the HSE’s Service Plan.
CannEpil® will be available free of charge to patients under the Long-Term Illness Scheme, GMS (Medical Card) Scheme,
and the Drugs Payment Scheme on a named patient basis and is an important step in providing Refractory Epilepsy
patients access to CannEpil® across Europe and improving their quality of life.
LICENCES AND DISTRIBUTION AGREEMENTS
Master Supply Agreement into US signed with AMC Holdings
Landmark agreement signed to enter the US with minimum orders of US$24 million for MGC products
including CannEpil®, CogniCann® and CimetrA™ over the initial 3-year period. As the licensed distributor of MGC
Pharma products in the USA, AMC will undertake all marketing activities in the US, as well as managing the import and
warehousing of the products. To assist with product development activities, AMC will also collect data from the end users
of the products for analysis by MGC Pharma.
13
This is the first dedicated supply agreement executed by MGC Pharma for the supply of MGC Pharma pharmaceutical
products into the USA, the largest healthcare market in the world. The Agreement with AMC is also an important step in
expediting the clinical trials process for both CannEpil® and CogniCann®, as well as providing access to these medicines
to more patients.
Master Supply and distribution agreement signed with Swiss PharmaCan AG for ArtemiC™
MGC Pharma signed a three-year exclusive worldwide supply and distribution agreement with leading European
nutraceuticals producer and distributor, Swiss PharmaCan AG (SPC), for the distribution of ArtemiC™ Rescue as a food
supplement.
This Agreement represents the first sales of ArtemiC™ as a food grade product and Swiss PharmaCan AG has agreed to a
minimum wholesale order quantity to MGC Pharma of 40,000 units per quarter of ArtemiC™ Rescue.
After the first agreement was signed, Swiss PharmaCan AG increased its initial purchase order by 85%. The first two
purchase orders have been received and provide revenues of circa $1,000,000 per quarter based on the minimum order
agreed.
UK Distribution agreement signed with LYPHE Group
MGC Pharma signed a distribution agreement with leading UK medicinal cannabis provider LYPHE Group Limited
(LYPHE), providing the Company direct access to LYPHE’s established distribution channels in the UK. LYPHE has
extensive networks and has developed a patient-access and distribution ecosystem which positions it as the leader in the
UK’s rapidly expanding medicinal cannabis market.
As part of the distribution agreement, LYPHE will prescribe and dispense the Company’s affordable MP Line products
under LYPHE labels to patients at its clinics.
IM Cannabis Corp Agreement for CannEpil® distribution
The Company executed a binding term sheet with IM Cannabis Corp. (IMC), one of the leading cannabis companies in
Israel with operations in Europe, for the exclusive wholesale import, sales, and distribution of CannEpil® in Israel.
Under the terms of the Agreement, IMC will be appointed as the exclusive wholesale importer of CannEpil® in Israel for a
period of five years provided it meets minimum annual sales levels.
CORPORATE
Listing on the London Stock Exchange
In February, MGC Pharmaceuticals successfully completed a £6.5million (circa $12million) placement to become the first
medicinal cannabis company to list on the London Stock Exchange.
The placement was supported by high quality UK institutions and supported by family offices and high net worth
investors. It will enable MGC Pharma to fund further clinical trials and scientific research into the use of medicinal
cannabis, expand its range of proprietary products and bolster its manufacturing capacities to meet the rapidly increasing
global demand.
Acquisition of Medicinal Cannabis Clinics
MGC Pharma signed a binding term sheet with Cannvalate Pty Ltd to acquire 100% of the operating clinic-based
assets, data and intellectual property of its wholly owned subsidiary Medicinal Cannabis Clinic (MCC). MCC is a leading
Australian medicinal cannabis clinic with a large and existing doctor and patient network. MGC Pharma’s acquisition of
MCC’s assets, along with its import and distribution capability will reduce supply chain costs which will in turn lead to
increasingly more affordable, high-quality cannabinoid medications for an expanding patient base across Australia.
Acquisition of MediCaNL - Driving efficiencies in medical research
MGC Pharma, through its acquisition of MediCaNL Inc., acquired MediCaNL Israel 2019 Ltd (MediCaNL), an Israeli
company operating in, and providing specialist services to the pharmaceutical sector for the development of new
medicines. MediCaNL offers clinical and preclinical trial services, as well as providing assistance with clinical trials,
including supplying research data from past Phase I to IV studies.
As part of the acquisition, MediCaNL will continue to work with its existing clients and its current 40 projects and clinical
trials. It will enable MGC Pharma to streamline the process of bringing medicines and products to market by increasing
its clinical trial capacity and making clinical trial performance and design an insourced activity. The acquisition will also
deliver significant and ongoing cost savings to the Company, with MGC Pharma undertaking a number of Phase I,
Phase II, and Phase III clinical trials.
As part of the agreement, Dr Nadya Lisodover, CEO of MediCaNL Inc, who had been working with MGC Pharmaceuticals
over the past two years, has joined permanently as MGC’s Chief Medical Officer.
14
Key appointments
MGC Pharma have made a number of key appointments to the company, to help drive growth in the next phase of the
company’s development. In the year the following appointments have been made:
■ Nicole Godresse, Global Chief Sales Officer: as part of its global sales strategy, MGC pharma appointed industry
leading sales executive Nicole Godresse to implement a focused, global growth strategy, beginning with Australia
and New Zealand. Nicole brings over 20 years’ experience in the pharmaceutical/healthcare industry, holding senior
commercial roles with major multi-national companies including Eli Lilly, Johnson & Johnson, Schering-Plough,
Merck Sharp & Dohme and most recently Tilray
■ Evan Hayes, Independent Non-Executive Director: Evan Hayes is a highly experienced Board member and brings over
20+ commercial and leadership experience within the healthcare and biotechnology sectors. Mr Hayes is currently the
Asia Pacific Managing Director of Factors Group, Canada’s largest natural health company. Prior to this Mr Hayes was
the Director of Sourcing and Product Development at Australia’s largest natural health company, Blackmores, leading
the Procurement, Technical, New product development, and Strategic sourcing divisions and managed a budget of
$250m.
OUTLOOK FOR THE PERIOD AHEAD
MGC Pharma anticipates significant growth in the coming year, both of its sales of existing product and in its clinical
pipeline. Via its existing relationships and through new distribution and access agreements in existing and new
geographies, MGC Pharma is focused on increasing sales in key markets as well as facilitating awareness and clinical
activities supporting the company’s product lines enroute to Market Authorisation.
MGC Pharma has taken significant steps towards becoming a global biopharma Company with a focus on
phytocannabinoid and plant-based treatments, available to patient populations in need around the world. Our research
and development agenda, coupled with our robust clinical platform, sets us at the forefront of this significant emerging
segment of the global pharmaceutical market. MGC Pharma intends to ensure our position over the coming years by
continually bringing products to markets with full market authorization and in keeping with global regulations, offering
cost effective treatments to patients with underserved indications the world over.
SUBSEQUENT TO FINANCIAL YEAR END
Subsequent to year end, the Company had the following events for disclosure:
On 8 July 2021 Mercer Street Global Opportunity Fund LLC elected to convert $500,000 of its convertible notes into
14,792,899 ordinary shares, leaving a balance of $2,100,000 (face value) in convertible notes at the date of this report.
On 12 August 2021 the Company held a General Meeting with performance rights issued to the Directors. As these
performance rights were agreed to be issued during the financial year, and have been expensed over the relevant service
conditions within the current year.
On 26 August, the Company executed a US$24 million supply agreement with AMC Holdings Inc of MGC Pharma
phytomedicine products over three years, with a minimum of US$3 million within the first year, subject to the grant of a
National Clinical Trial Number.
Significant Changes in State of Affairs
In the opinion of the Directors, there have been no significant changes to the state of affairs of the Group during the year
other than those disclosed elsewhere in the financial report or the notes thereto.
ENVIRONMENTAL REGULATIONS AND PERFORMANCE
The Group’s operations are subject to various environmental laws and regulations under the relevant Governments’
legislation. Full compliance with these laws and regulations is regarded as a minimum standard for all operations to
achieve. There have been no significant known breaches by the Group during the financial year.
FUTURE DEVELOPMENTS, PROSPECTS AND BUSINESS STRATEGIES
The Company will continue to pursue its clinical trials on its CimetrA™, CannEpil® and CogniCann® products, along with
preclinical trials in fighting Glioblastoma, an aggressive brain cancer, using a novel combination of cannabinoids.
MGC Pharma is also continuing to grow its sales of phytomedicine products globally, through both existing distribution
channels and new territories.
15
PRODUCT
CATALOGUE
CannEpil
PHYTOCANNABINOID MEDICINES
Cognicann
PHYTOCANNABINOID MEDICINES
CannEpil is a formulation of
phytocannabinoids delivered
as an oral solution to treat
refractory epilepsy (drug
resistant epilepsy).
Formulation: Cannabidiol
(CBD) 100 mg/mL Delta-9-
Tetrahydrocannabinol (THC)
5 mg/mL.
Cognicann is a formulation
of phytocannabinoids
delivered as an oral
solution to treat dementia
and Alzheimer’s.
Formulation: Delta-9-
Tetrahydrocannabinol
(THC) 25 mg/mL
Cannabidiol (CBD)
17 mg/mL.
CimetrA™
P L A N T BA S E D T H E R A PY
ArtemiCTM
P L A N T BA S E D T H E R A PY
CimetrA™ is an Investigational
Medical Product which has
clinically proven effect in
arresting the Cytokine Storm
in COVID-19 patients.
Compounds: Combination
of Curcumin and Boswellia
Serrata: Medical oral spray
Mechanism of action:
Immunomodulation in
inflammatory conditions.
16
ArtemiC™ Rescue (ArtemiC™) is
designed with the scientific aim to
target viral infections with inflammatory
complications and was successfully
evaluated on COVID-19 infected
patients in a double-blind, placebo
controlled, Phase II clinical trial.
Compounds: Combination
of Ascorbic Acid, Curcumin,
Boswellia Serrata and
Artemisinin Administration:
Medical oral spray Mechanism
of action: Immunomodulation
in inflammatory conditions.
MP 100
PHYTOCANNABINOID RATIO PRODUCTS
MP 1:30
PHYTOCANNABINOID RATIO PRODUCTS
MP 100 is a Phytocannabinoid
based product containing
Cannabidiol (CBD) in an
oil vehicle. 1 ml of MP 100
contains 25 mg of THC and 1.7
mg of CBD.
MP 1:30 is a Phytocannabinoid
based product containing
Tetrahydrocannabinol (THC)
and Cannabidiol (CBD) in an
oil vehicle. 1 ml of MP 1:30
contains 100 mg of THC and
3.3 mg of CBD.
MP 1:1
PHYTOCANNABINOID RATIO PRODUCTS
MP 15:1
PHYTOCANNABINOID RATIO PRODUCTS
MP 1:1 is a Phytocannabinoid
based product containing
Tetrahydrocannabinol (THC)
and Cannabidiol (CBD) in an oil
vehicle. 1 ml of MP 1:1 contains
100 mg of CBD.
MP 15:1 is a Phytocannabinoid
based product containing
Tetrahydrocannabinol (THC)
and Cannabidiol (CBD) in an
oil vehicle. 1 ml of MP 15:1
contains 25 mg of THC and
1.7 mg of CBD.
MP 25T
PHYTOCANNABINOID RATIO PRODUCTS
MP 25T is a Phytocannabinoid
based product containing
Tetrahydrocannabinol (THC) in
an oil vehicle. 1 ml of MP 25T
contains 25 mg of THC.
ROBUST PIPELINE, DEMONSTRATING
THE EFFICACY AND VALUE OF
PLANT-BASED PRODUCTS
17
INFORMATION ON DIRECTORS AND SECRETARIES
Names, special responsibilities, qualifications and experience of current directors and company secretaries:
Brett Mitchell, B. Ec - Executive Chairman
Mr Mitchell is a corporate finance executive with over 25 years of experience in the venture capital, equity capital markets,
technology and resources sectors. He has been involved in the founding, financing and management of both private and
publicly listed companies, and was instrumental in the successful LSE listing for MGC Pharma in February 2021.
Mr Mitchell is a founder and director of Chieftain Securities Pty Ltd, a Perth based Corporate Advisory & Venture Capital
firm and founder and shareholder of Graft Polymer (UK) Ltd. Mr Mitchell is also currently Non-Executive Director of
ASX Listed company Red Dirt Metals Limited (RDT), and Executive Chairman of an Australian unlisted public company,
Australian Cannabis Ventures Limited.
Interest in MGC securities held as at date of this report
Mr Brett Mitchell and Mrs Michelle Mitchell (jointly controlled)
22,542,221 Fully Paid Ordinary Shares
20,000,000 Performance Rights
Mr Brett and Mrs Michelle Mitchell (jointly controlled)
8,418,337 Fully Paid Ordinary Shares
12,400,000 Performance Rights
YCAGAGF Investments Pty Ltd (Mr Mitchell is a Director and holds a 33% shareholding)
1,500,000 unlisted options exercisable at $0.05 expiring 31 August 2023
1,500,000 unlisted options exercisable at $0.06 expiring 31 August 2023
1,500,000 unlisted options exercisable at $0.07 expiring 31 August 2023
Directorships held in other ASX listed entities in the past three years
Red Dirt Metals Limited (27 June 2017 – current)
Sky and Space Global Ltd (12 May 2016 – 31 October 2018)
Roby Zomer – Managing Director and CEO
Mr. Zomer was recruited into MGC Pharma by its founders at the inception of the Company and has since served in
multiple roles within MGC Pharma, culminating with his current role as MD and CEO. With ten years of experience in large
scale projects in the Biotech and Agrotech sectors, Mr. Zomer has been crucial in moving MGC Pharma from a cannabis
concept to a fully functioning biopharma company with global activities. This was part of the vision that has allowed MGC
Pharma to launch, and divest itself of, both a Cannabis Cosmetic company (MGC Derma) and a Lifestyle Company (MGC
Nutra), which were both crucial building blocks to centralising the Company’s pharma vision and activities.
Over the past year, Mr Zomer has been crucial to solidifying the Company’s standing as a leading provider of
phytomedicines in several regions globally, has successfully launched and derived revenue from ArtemiCTM. Additionally,
he has put his engineering and medical background into play and has put significant emphasis on the Company’s
research and development activities, leading to possibilities of distribution and collaboration in several compelling
markets around the globe.
Interest in MGC securities held as at date of this report
Chitta Lu Limited (an entity controlled by Mr Zomer)
3,000,001 Fully Paid Ordinary Shares
32,400,000 Performance Rights
HSBC Custody Nominees (Australia) Limited (shares held via custodial account)
30,000,000 Fully Paid Ordinary Shares
Directorships held in other ASX listed entities in the past three years
Nil.
Nativ Segev – Non-Executive Director
Mr Segev founded MGC Pharma in 2014 with a goal to expand into international markets and raise the quality of medicinal
phytocannabinoid products, in addition to making them accessible to patients all over the world. Prior to establishing MGC
Pharma, Mr. Segev was a leader in the Medical Cannabis industry with a sizeable patient-base.
He has over 10 years of experience in implementation, legislation and lobbying in the global Medical Cannabis industry,
combined with over 15 years of experience in diverse executive roles.
18
Interest in MGC securities held as at date of this report
Nativ Segev
1 Fully Paid Ordinary Share
Brighght Global Limited (an entity controlled by Mr Segev)
500,000 Fully Paid Ordinary Shares
2,100,000 Performance Rights
HSBC Custody Nominees (Australia) Limited (shares held via custodial account)
52,500,000 Fully Paid Ordinary Shares
Directorships held in other ASX listed entities in the past three years
Nil.
Dr Ross Walker, MBBS (Hons), FRACP, FCSANZ - Non-Executive Director and Chairman of Strategic Advisory Board
Dr Ross Walker is an eminent practicing cardiologist with over 35 years’ experience as a clinician. For the past 20 years, he
has been focusing on preventative cardiology and is one of Australia’s leading preventative health experts.
Dr Walker is considered one of the world’s best keynote speakers and life coaches, he is the author of seven best-selling
books and a health presenter in the Australian Media
Interest in MGC securities held as at date of this report
Ross G T Walker Pty Ltd (an entity controlled by Mr Walker)
4,370,370 Fully Paid Ordinary Shares
2,100,000 Performance Rights
Directorships held in other ASX listed entities in the past three years
Nil.
Dr Stephen Parker, D. Phil, MBA – Senior Independent Director and Chairman of the Corporate Governance
Committees
Dr Stephen Parker is a seasoned executive with over thirty years’ experience in the pharmaceuticals and biotechnology
sectors, as a senior executive in the sector, a strategic consultant, a venture capitalist and a senior corporate financier
with Baring’s, Warburg’s and Apax Partners. Dr Parker is currently Chairman of Sareum Holdings plc and a non-Executive
Director of Eternans Limited. Stephen has a D.Phil. from Oxford University and an MBA from City University Business
School.
Interest in MGC securities held as at date of this report
Dr Stephen Parker
2,600,000 Performance Rights
Held through a UK Individual Savings Account (Barclays Bank PLC)
282,316 Fully Paid Ordinary Shares
Directorships held in other ASX listed entities in the past three years
Nil.
Evan Hayes, MSC Biotech, BSC BioChem, NICM Adjunct Fellow, GAICD, MASM – Non-Executive Director
Evan Hayes was appointed a Non-executive director of the Company on 1 September 2020. Mr Hayes is a highly
experienced Board member and brings over 20+ commercial and leadership experience within the healthcare and
biotechnology sectors. Mr Hayes graduated with a Master of Science 1st Class Honours (Biotechnology) from the
National University of Ireland, Galway and prior to this he finished first in his class from the National University of Ireland,
Cork with a Bachelor of Science degree (Honours). Mr Hayes’ has also won the Daniel O’Carroll Award for Scientific
Research.
Mr Hayes is currently the Asia Pacific Managing Director of Factors Group, Canada’s largest natural health company.
Prior to this Mr Hayes was the Director of Sourcing and Product development at Australia’s largest natural health
company, Blackmores, leading the Procurement, Technical, New product development, and Strategic sourcing divisions
and managed a budget of $250m. Evan has served on multiple boards, worked in Europe the USA and in Australia
evidenced by his strong knowledge of both the FDA and the TGA. Mr Hayes is an author of multiple patents including one
world patent.
19
Interest in MGC securities held as at date of this report
Evan Hayes
2,600,000 Performance Rights
Directorships held in other ASX listed entities in the past three years
New Zealand Coastal Seafoods Limited (25 Jan 2021 – current)
David Lim – Company Secretary
Mr Lim is a finance and corporate governance professional with over 15 years of experience working for ASX Listed
companies. He has previously performed the role of Group CFO and Company Secretary at a number of ASX listed
businesses including Equigold NL, Reed Resources Ltd, Aurora Oil and Gas Ltd and Elixir Petroleum Ltd
Mr Lim is a Certified Practicing Accountant and holds a Graduate Diploma of Applied Corporate Governance from, and is
an Associate member of, the Governance Institute of Australia.
Rachel Kerr – Company Secretary
Mrs Kerr has over 10 years’ experience as a Company Secretary on both private and public companies, managing a
number of acquisitions, capital raisings, IPO’s, due diligence reviews and the compliance of public companies.
Remuneration Report (Audited)
This report details the nature and amount of remuneration for each key management person of MGC Pharmaceuticals
Ltd, and for the executives receiving the highest remuneration.
Remuneration Policy
The remuneration policy of MGC Pharmaceuticals Ltd has been designed to align key management personnel objectives
with shareholder and business objectives by providing a fixed remuneration component and offering specific long-term
incentives based on key performance areas affecting the consolidated group’s financial results. The Board of MGC
Pharmaceuticals Ltd believes the remuneration policy to be appropriate and effective in its ability to attract and retain
the best key management personnel to run and manage the Group, as well as create goal congruence between directors,
executives and shareholders.
The Board’s policy for determining the nature and amount of remuneration for key management personnel of the Group is
as follows:
■ The remuneration policy, setting the terms and conditions for the key management personnel, was developed and
approved by the Board.
■ All key management personnel receive a base salary (which is based on factors such as length of service and
experience), superannuation, fringe benefits and performance incentives.
■ The Board reviews key management personnel packages annually by reference to the consolidated group’s
performance, executive performance and comparable information from industry sectors.
The performance of key management personnel is measured against criteria agreed annually with each executive and is
based predominantly on the forecast growth of the Group’s profits and shareholders’ value. All bonuses and incentives
must be linked to predetermined performance criteria. The Board may, however, exercise its discretion in relation to
approving incentives, bonuses and options. Any changes must be justified by reference to measurable performance
criteria. The policy is designed to attract the highest calibre of executives and reward them for performance that results in
long-term growth in shareholder wealth.
Key management personnel are also entitled to participate in the employee security arrangements.
All remuneration paid to key management personnel is valued at the cost to the Company and expensed. Shares given to
key management personnel are valued as the difference between the market price of those shares and the amount paid
by key management personnel. Options and other convertible securities are valued using the Black-Scholes methodology.
20
The Board policy is to remunerate Non-Executive Directors at market rates for time, commitment, and responsibilities.
The Board determines payments to the Non-Executive Directors and reviews their remuneration annually, based on
market practice, duties, and accountability. Independent external advice is sought when required. The maximum
aggregate amount of fees that can be paid to Non-Executive Directors is subject to approval by shareholders at the Annual
General Meeting. Fees for Non-Executive Directors are not linked to the performance of the consolidated group. However,
to align directors’ interests with shareholder interests, the Directors are encouraged to hold shares in the Company and
are able to participate in the employee securities plan.
At the 2020 Annual General Meeting, the Company received 35.28% of votes against the non-binding resolution to approve
the 2020 remuneration report. It was noted the votes against only represented 2.92% of the issued Capital at that time,
and a number of changes were made to service agreements with the Directors with effect from 1 July 2020. Both the
remuneration committee and Board feel the current remuneration is commensurable with a Company of its size and
complexity.
Performance-based Remuneration
During the year, discretionary cash bonuses were issued as a reward for the successful IPO on the London Stock
Exchange. In addition, the Board deemed it appropriate to ensure both management and the Directors had incentive
performance rights issued. These performance rights are considered a combination of service-based criteria and
milestones linked to share price growth. The Board considers this appropriate, as it aligns with creating shareholder value
and also assists retaining key people which are paid at or below market rates to reduce cash outlay.
Company Performance, Shareholder Wealth and Director and Executive Remuneration
Overview of Company Performance
The table below sets out information about MGC Pharmaceuticals Ltd’s earnings and movements in shareholder wealth
for the past five years up to and including the current financial year.
30 JUNE 2021
30 JUNE 2020
Net loss after tax ($)
Share price at year end ($)
Basic loss per share (cents)
Dividends paid
* The net loss after tax and basic loss per share presented for each period prior to 30 June 2020 have been restated as a result of the
(19,370,226)
0.02
(1.40)
-
(15,871,978)
0.037
(0.83)
-
30 JUNE 2019
(RESTATED)*
(8,623,856)
0.052
(0.71)
-
30 JUNE 2018
(RESTATED)*
(7,089,432)
0.066
(0.56)
-
30 JUNE 2017
(RESTATED)*
(7,212,025)
0.046
(0.71)
-
correction of the prior period error disclosed in the 2020 financial statements.
Key Management Personnel Remuneration Policy
The Board’s policy for determining the nature and amount of remuneration of key management for the Group is as follows:
The remuneration structure for key management personnel is based on a number of factors, including length of service,
particular experience of the individual concerned, and overall performance of the Company. The contracts for service
between the Company and key management personnel are on a continuing basis, the terms of which are not expected
to change in the immediate future. Upon retirement key management personnel are paid employee benefit entitlements
accrued to date of retirement.
21
All Directors had contracts in place with the Company during the financial year as detailed below.
Material terms of agreements in place during the financial year:
BRETT MITCHELL, EXECUTIVE CHAIRMAN
■ Director Agreement dated 1 July 2020, no termination date or payment on termination;
■ $4,000 per month.
■ MGC Pharma (UK) Ltd Non-Executive Director agreement commenced 30 June 2016; no termination date or payment on termination;
■ Fees of £910 per month.
Addendum to Services Agreement with Sibella Capital Pty Ltd, an entity controlled by Mr Mitchell, valid from 1 March 2021
■ MGC Pharmaceuticals Ltd executive services agreement. This is a 12-month rolling contract with 90 days’ notice and no termination
fee payable;
■ Fees increased from $12,000 per month to £14,000 per month.
■ Performance Rights as approved at the General Meeting on 12 August 2021.
ROBY ZOMER, CEO & MANAGING DIRECTOR
■ Director Agreement dated 1 July 2020, no termination date or payment on termination;
■ Standard director fee of $4,000 per month.
■ MGC Pharma (UK) Ltd Non-Executive Director agreement commenced 30 June 2016; no termination date or payment on termination;
■ Fees of £910 per month.
■ MGC Pharmaceuticals d.o.o (the Group’s Slovenian subsidiary) director agreement commenced 1 July 2018; no termination date or
payment on termination;
■ Fees of €1,024 per month (excluding taxes).
Addendum to Services Agreement with Chitta Lu Limited, an entity controlled by Mr Zomer, valid from 1 March 2021
■ MGC Pharmaceuticals Ltd executive services agreement. This is a 12-month rolling contract with 90 days’ notice and no termination
fee payable;
■ Fees increased from $12,500 per month to £14,500 per month.
■ Performance Rights as approved at the General Meeting on 12 August 2021.
MR NATIV SEGEV, NON-EXECUTIVE DIRECTOR - CURRENT DIRECTOR AGREEMENT
■ Director Agreement dated 1 July 2020, no termination date or payment on termination;
■ Standard director fee of $4,000 per month.
Services Agreement with Brighght Global Limited, an entity controlled by Mr Segev, valid from 1 July 2020 to current
■ MGC Pharmaceuticals Ltd services agreement this automatically renews every 12 months unless terminated, 90 days’ notice;
■ Fees reduced to $5,000 per month.
■ No termination fee payable.
DR ROSS WALKER, NON-EXECUTIVE DIRECTOR AND CHAIRMAN OF STRATEGIC ADVISORY BOARD
■ Director Agreement dated 1 July 2020, no termination date or payment on termination;
■ Non-Executive Director fees of $4,000 per month.
DR STEPHEN PARKER, SENIOR INDEPENDENT DIRECTOR AND CHAIRMAN OF THE CORPORATE GOVERNANCE
COMMITTEES
■ Director Agreement dated 1 July 2020, no termination date or payment on termination;
■ Non-Executive Director fees of $4,000 per month.
■ With effect from 1 April 2021 an additional $1,000 per month for acting as the Strategic Independent Director and acting as the
Chairman of the Corporate Governance Committees.
DR EVAN HAYES, NON-EXECUTIVE DIRECTOR
■ Director Agreement dated 1 September 2020, no termination date or payment on termination;
■ Non-Executive Director fees of $4,000 per month.
In accordance with clause 14.7 and 14.8 of the Company’s constitution, the total aggregate fixed sum per annum to be
paid to non-executive Directors, for Director related services, shall not exceed $250,000 and may be varied by ordinary
resolution of the shareholders at a general meeting.
22
Details of Remuneration
Key Management Personnel Remuneration
CASH
SHORT-TERM BENEFITS
PERFOR-
MANCE
BONUS OTHERii
CASH
AND
SALARY
NON-CASH
POST-EMPLOYMENT BENEFITS
SUPER-
ANNUATION
TERMINATION
BENEFITS
SHARE
BASED
PAYMENTSi
PERFOR-
MANCE
RELATED %
TOTAL
EQUITY
-
-
-
-
-
-
-
-
-
-
-
-
-
-
50,000
50,000
-
-
-
-
267,397
280,556
107,540
48,000
56,557
40,000
800,050
-
(9,620)
(28,462)
-
-
-
100,000 (38,082)
DIRECTORS
2021
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayesiii
Total
2020
230,532
Brett Mitchell
290,319
Roby Zomer
240,319
Nativ Segev
52,000
Ross Walker
60,608
Stephen Parker
873,778
Total
All Directors have contracts with the Company.
i. Refer to Share-based and other performance based compensation section below for detail.
II. “Other” includes expat expenses in Malta and Slovenia. During the current year, credit notes were issued against these expenses that
477,705
481,244
106,460
75,382
84,867
68,310
432,000 1,293,968
351,988
439,986
265,520
52,000
60,608
124,391 1,170,102
160,308
160,308
27,382
27,382
28,310
28,310
30,000
30,000
30,000
-
-
90,000
-
28,211
53,722
-
-
81,933
91,456
91,456
(58,521)
-
-
44.02%
43.70%
25.72%
36.32%
33.36%
41.44%
22.43%
17.95%
5.26%
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
were expensed and unpaid at 30 June 2020, as a result of cost reductions due to Covid-19.
iii. Mr Evan Hayes was appointed a director of the Company on 1 September 2020.
Option Holdings of Key Management Personnel
DIRECTORS
2021
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayesii
Total
2020
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Total
OPENING BALANCE
GRANTED AS
COMPENSATION
OPTIONS
EXERCISED
NET OTHER
CHANGES
CLOSING BALANCE
(VESTED AND
EXERCISABLE)
9,500,000
-
-
-
-
-
9,500,000
5,000,000
-
-
-
-
5,000,000
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
(4,444,446)i
-
-
-
-
-
(4,444,446)
4,500,000
-
-
-
-
4,500,000
5,055,554
-
-
-
-
-
5,055,554
9,500,000iii
-
-
-
-
9,500,000
i. 5,000,000 of the 9,500,000 options held by YCAGAGF Investments Pty Ltd, of which Mr Mitchell, is a director expired unexercised
on 30 June 2021, 555,554 Listed Options were granted to Trusts controlled by Mr Mitchell as part of a placement undertaken in
July 2020.
ii. Mr Evan Hayes was appointed a director of the Company on 1 September 2020.
iii. Chieftain Securities Pty Ltd held these options of which Mr Mitchell is a director and 25% shareholder.
23
Performance Rights held by Key Management Personnel
Details of performance rights held directly, indirectly or beneficially by KMP and their related parties are as follows:
DIRECTORS
2021
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayesiv
Total
2020
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Total
OPENING BALANCE
GRANTED AS
COMPENSATIONi
PERFORMANCE
RIGHTS EXERCISED
NET OTHER
CHANGES
CLOSING BALANCE
10,000,000
10,000,000
-
-
-
-
20,000,000
-
-
-
-
-
-
-
(2,500,000)
(2,500,000)
-
-
-
-
(5,000,000)
(2,500,000)ii
(2,500,000)ii
-
-
-
-
(5,000,000)
-
-
-
-
-
-
10,000,000
10,000,000
-
-
-
20,000,000
-
-
-
-
-
-
-
-
-
-
-
-
5,000,000iii
5,000,000iii
-
-
-
-
10,000,000
10,000,000
10,000,000
-
-
-
20,000,000
i. Refer to “Share-based and other performance-based compensation” section below for details of rights granted and vested during the
period, which were still subject to shareholder approval at 30 June 2021 and therefore had not yet been issued.
ii. Lapsed as Milestones not satisfied.
iii. 5,000,000 unvested at balance date.
iv. Mr Evan Hayes was appointed a director of the Company on 1 September 2020.
Shareholdings of Key Management Personnel
Details of equity instruments (other than options and rights) held directly, indirectly or beneficially by KMP and their parties
are as follows:
Shareholdings
DIRECTORS
2021
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayesiii
Total
2020
Brett Mitchell
Roby Zomer
Nativ Segev
Ross Walker
Stephen Parker
Evan Hayesiii
Total
OPENING BALANCE
GRANTED AS
COMPENSATION
PERFORMANCE
RIGHTS EXERCISED
NET OTHER
CHANGES
CLOSING BALANCE
27,905,004
30,500,001
53,000,001
4,370,370
-
-
115,775,376
26,793,894
30,500,001
53,000,001
4,000,000
-
-
114,293,896
-
-
-
-
-
-
-
-
-
-
-
-
-
-
2,500,000
2,500,000
-
-
-
-
5,000,000
-
-
-
-
-
-
-
-
-
-
-
282,316ii
-
282,316
1,111,110i
-
-
370,370i
-
-
1,481,480
30,405,004
33,000,001
53,000,001
4,370,370
282,316
-
121,057,692
27,905,004
30,500,001
53,000,001
4,370,370
-
-
115,775,376
i. Net other changes are as a result of rights allotted as part of the Share Purchase Plan issue and other movement due to changes in
directors and directors’ related entities.
ii. Acquired on market.
iii. Mr Evan Hayes was appointed a director of the Company on 1 September 2020.
24
Share-based and other performance-based compensation
Performance rights
On 31 March 2021, the remuneration committee agreed to issue performance rights to the Directors and other
management personnel, to incentivise and retain its workforce. The performance rights issued to Directors were subject
to shareholder approval, which was received subsequent to year-end on 12 August 2021 (grant date):
#
A
B
C
VESTING MILESTONE
If and once the share price of MGC Pharma, at any time prior to or
on 1 April 2022, has a 10- trading day VWAP equal to or exceeding
$0.0875 and the participant remaining a director as at 1 April 2022
If and once the share price of MGC Pharma, at any time prior to or on
1 April 2023, has a 10- trading day VWAP equal to or exceeding $0.105
and the participant remaining a director as at 1 April 2022
18 months continued service up to 30 June 2021 or if employment
commenced after 1 January 2020, continued employment from the
commencement date until 30 June 2021
PERFORMANCE RIGHTS MILESTONE DATE
17,100,000
1 Apr 22
39,900,000
1 Apr 23
7,200,000
64,200,000
30 Jun 21
The performance conditions were chosen to best align with the Company’s strategic goals and objectives to enhance
shareholder value. There was no performance condition associated with Milestone C. The grant of the performance
rights, including those without performance conditions, is considered by the Company to be a reasonable and appropriate
method to provide cost effective remuneration as the non-cash form of this benefit will allow the Company to spend a
greater proportion of its cash reserves on its operations than it would if alternative cash forms of remuneration were given
to the Related Parties
The fair value of the performance rights for milestones C was estimated to be $0.041/right at 30 June 2021. A Monte
Carlo valuation was applied to milestones A and B to estimate the fair values at 30 June 2021, with the following inputs
and assumptions:
Valuation date
Share price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Vesting hurdle
Dividend yield
Value per right
MILESTONE A
12 Aug 21
$0.041
Nil
1 Apr 22
66%
0.0355%
$0.0875
nil
$0.038
MILESTONE B
12 Aug 21
$0.041
Nil
1 Apr 23
70%
0.0388%
$0.105
nil
$0.009
Although grant date has occurred subsequent to year-end, there was an agreement in place during the year to issue the
performance rights, and therefore they have been expensed over the relevant service periods based on an estimated
valuation at 30 June 2021, which was consistent to the valuation subsequently determined at the grant date of
12 August 2021. The milestone C performance rights fully vested during the period, while the milestone A and B rights
remained unvested and are being expensed over the service period to 1 April 2022.
Performance bonuses
During the year, the Remuneration and Nomination Committee reviewed the performance of the executive team, and
concluded that a cash bonuses were to be issued to those that assisted with the LSE Listing. The executive Directors,
namely Mr Roby Zomer and Mr Brett Mitchell, both received an amount of $50,000 during the year.
Options
There were no options over ordinary shares granted to and/or vested by directors and other key management personnel
as part of compensation during the year ended 30 June 2021 or 30 June 2020.
25
Transactions with Director related entities
Directors and officers, or their personally-related entities, hold positions in other entities that result in them having controls
or significant influence over the financial or operating policies of those entities.
Details of non-remuneration related transactions including amounts receivable and payable at the end of the year are as follows:
RELATED PARTY
CHIEFTAIN SECURITIES
PTY LTD (CHIEFTAIN)
CHIEFTAIN SECURITIES
PTY LTD (CHIEFTAIN)
CHIEFTAIN SECURITIES
(WA) PTY LTD
(CHIEFTAIN WA)
GRAFT POLYMER (UK)
LIMITED
AUSTRALIA CANNABIS
VENTURES LIMITED
(ACV)
RELATIONSHIP NATURE OF TRANSACTIONS
(i)
(i)
(ii)
(iii)
(iv)
Corporate services from
Chieftain – 1 Jul 20 to 31 Dec 20
Charges from Chieftain for
capital raising costs
Corporate services from
Chieftain – 1 Jan 21 to
30 June 21
Services charges from/
(recharges to) GPO for
development for MGC Proprietary
drug delivery technology
(Re-charges) to ACV for
corporate administrative costs
TRANSACTIONS
FULL YEAR
30-JUN-21
$
FULL YEAR
30-JUN-20
$
BALANCES
(OWING TO)/ OWED BY
FULL YEAR
30-JUN-21
$
FULL YEAR
30-JUN-20
$
30,000
60,000
-
116,594
30,000
-
-
-
-
(5,500)
-
-
409,446
510,859
(6,820)
(40,000)
(10,000)
-
-
-
(i) Mr Brett Mitchell is a Director and holds a 25% shareholding in Chieftain Securities Pty Ltd.
(ii) Mr Brett Mitchell is a Director and holds a 25% shareholding in Chieftain Securities (WA) Pty Ltd.
(iii)
Mr Roby Zomer is Executive Chairman and shareholder of Graft Polymer (UK) Limited, who is developing the proprietary
nano-emulsion and nano-particle drug delivery platform for MGC Pharma medicines.
(iv) Mr Brett Mitchell is an Executive Chairman and shareholder of Australian Cannabis Ventures Limited.
End of Remuneration Report
Meetings of Directors
The Directors attendances at Board meetings held during the year were:
BOARD MEETINGS
Brett Mitchell
Nativ Segev
Roby Zomer
Ross Walker
Stephen Parker
Evan Hayes
HELD
6
6
6
6
6
6
ATTENDED
6
6
6
6
6
6
The Company has remuneration, nomination and audit and risk committees in place. The attendances of the Committee
Members for the meetings held during the year were:
Brett Mitchell
Ross Walker
Stephen Parker
REMUNERATION COMMITTEE
ATTENDED
2
2
2
HELD
2
2
2
NOMINATION COMMITTEE
ATTENDED
1
1
1
HELD
1
1
1
AUDIT AND RISK COMMITTEE
HELD
2
2
2
ATTENDED
2
2
2
Mr Evan Hayes was added to each of the sub-committees during the year, but not during the time any meetings were held.
26
Corporate Governance
In recognising the need for the highest standards of corporate behaviour and accountability, the Directors of MGC
Pharmaceuticals Ltd support and have adhered to the principles of sound corporate governance. The Board recognises
the recommendations of the Australian Securities Exchange Corporate Governance Council, and considers that the
Company is in compliance with many of those guidelines which are of importance to the commercial operation of the
Company. During the financial year, shareholders continued to receive the benefit of an efficient and cost-effective
corporate governance policy for the Company. The Company’s Corporate Governance Policy is available for review on
the Company’s website www.mgcpharma.com.au.
Options
At the date of this report the options on issue for MGC Pharmaceuticals Ltd are as follows:
DATE OF EXPIRY
31 August 2023
31 August 2023
31 August 2023
31 March 2023
31 March 2023
TOTAL
EXERCISE PRICE
$0.05
$0.06
$0.07
$0.026
£0.01475
Rights
At the date of this report the performance rights on issue for MGC Pharmaceuticals Ltd are as follows:
DESCRIPTION
Dec 19 Director Rights
Apr 21 Employee class A
Apr 21 Employee class B
Apr 21 Employee class C
Apr 21 Director class A
Apr 21 Director class B
Apr 21 Director class C
TOTAL
EXERCISE PRICE
nil
nil
nil
nil
nil
nil
nil
VESTED (YES/NO)
no
no
no
yes
no
no
yes
NUMBER
16,300,000
17,500,000
17,500,000
7,692,308
26,440,678
85,432,986
NUMBER
10,000,000
3,725,000
9,275,000
10,600,000
17,100,000
39,900,000
7,200,000
97,800,000
Convertible Notes
At the date of this report the convertible notes on issue for MGC Pharmaceuticals Ltd are as follows:
ISSUE DATE
20 November 2020
CONVERSION PRICE
$0.0351
FACE VALUE PER SECURITY
$1.00
MATURITY DATE
20 November 2021
NUMBER
2,100,000
1. The conversion price will be the lower of $0.035 or 92% of the lowest daily VWAP of the Company’s shares selected by Mercer over
the 10 trading days on which the Company’s shares are traded on the ASX immediately prior to the issue of the conversion notice,
subject to the conversion price being no less than $0.018
Indemnifying Officers or Auditor
The Company has given an indemnity or entered into an agreement to indemnify, or paid or agreed to pay insurance
premiums as follows:
The Company has paid premiums to insure all of the Directors of the Company as named above, the company secretary
and all executive officers of the Company against any liability incurred as such by a director, secretary or executive officer
to the extent permitted by the Corporations Act 2001. The contract of insurance prohibits disclosure of the notice of the
liability and the amount of the premium.
To the extent permitted by law, the Company has agreed to indemnify its auditors, Ernst & Young Australia, as part of
the terms of its audit engagement agreement against claims by third parties arising from the audit (for an unspecified
amount). No payment has been made to indemnify Ernst & Young Australia during or since the financial year.
Proceedings on behalf of Company
No person has applied for leave of Court to bring proceedings on behalf of the Company or intervene in any proceedings
to which the Company is a party for the purpose of taking responsibility on behalf of the Company for all or any part of
those proceedings. The Company was not a party to any such proceedings during the year.
27
Non-audit Services
The following non-audit services were provided by the entity’s auditor, Ernst & Young Australia. The directors are satisfied
that the provision of non-audit services is compatible with the general standard of independence for auditors imposed
by the Corporations Act 2001. The nature and scope of each type of non-audit service provided means that auditor
independence was not compromised.
Ernst & Young Australia received or are due to receive $40,580 for the provision of non-audit services in relation to the
Group’s R&D rebate application for the 2020 financial year.
Auditor’s Independence Declaration
The lead auditor’s independence declaration for the year ended 30 June 2021 has been received and can be found on
page 29 of the financial report.
This report is made in accordance with a resolution of Directors. These financial statements were authorised for issue in
accordance with a resolution by the Directors of the Company on 29 September 2021.
Roby Zomer
Managing Director
Dated 30 September 2021
28
06
AUDITOR’S INDEPENDENCE
DECLARATION
Auditor’s independence declaration to the directors of MGC Pharmaceuticals
Limited
As lead auditor for the audit of the financial report of MGC Pharmaceuticals Limited for the financial
year ended 30 June 2021, I declare to the best of my knowledge and belief, there have been:
a. No contraventions of the auditor independence requirements of the Corporations Act 2001 in
relation to the audit; and
b. No contraventions of any applicable code of professional conduct in relation to the audit.
This declaration is in respect of MGC Pharmaceuticals Limited and the entities it controlled during the
financial year.
Ernst & Young
Timothy Dachs
Partner
30 September 2021
A member firm of Ernst & Young Global Limited
Liability limited by a scheme approved under Professional Standards Legislation
TD:TGF:MGC:004
29
07
CONSOLIDATED STATEMENT
OF PROFIT OR LOSS
Consolidated Statement of Profit or Loss and Other
Comprehensive Income
Note
5a)
6a)
5c)
6b)
6c)
20
6d)
6e)
5b)
7
4
For the year ended 30 June 2021
Continuing operations
Revenue from contracts with customers
Cost of sales
Gross profit
Other operating income
Administrative expenses
Other operating expenses
Fair value movement on financial instruments
Write-off/impairment expense
Operating loss
Finance costs
Finance income
Other income
Loss before income tax from continuing operations
Income tax expense
Loss for the year from continuing operations
Discontinued operations
Loss after tax for the year from discontinued operations
Loss for the year
Attributable to:
Members of the parent entity
Non-controlling interest
Other comprehensive income for the year
Items that may be reclassified subsequently to profit or loss
Exchange differences on the translation of foreign operations
Other comprehensive income (net of tax) for the year
Total comprehensive loss for the year
Total comprehensive loss attributable to:
Members of the parent entity
Non-controlling interest
Earnings per share
Basic loss for the year attributable to ordinary equity holders of the parent
Diluted loss for the year attributable to ordinary equity holders of the parent
Earnings per share for continuing operations
Basic loss for the year attributable to ordinary equity holders of the parent
Diluted loss for the year attributable to ordinary equity holders of the parent
18
18
18
18
The accompanying notes form part of these financial statements
30
30-Jun-21
$
2,962,897
(1,652,485)
1,310,412
606,745
(8,287,864)
(5,250,690)
(3,704,592)
-
(15,325,989)
(369,135)
7,632
250,873
(15,436,619)
30-Jun-20
$
2,079,169
(1,904,504)
174,665
518,851
(6,609,147)
(5,520,556)
(2,098,064)
(5,117,767)
(18,652,018)
(135,582)
12,336
5,465
(18,769,799)
27,278
(15,409,341)
-
(18,769,799)
(462,637)
(15,871,978)
(600,427)
(19,370,226)
(15,869,978)
(2,000)
(15,871,978)
(19,363,089)
(7,137)
(19,370,226)
131,416
131,416
51,356
51,356
(15,740,562)
(19,318,870)
(15,738,244)
(2,318)
(15,740,562)
(19,311,733)
(7,137)
(19,318,870)
(0.83)
(0.83)
(0.81)
(0.81)
(1.40)
(1.40)
(1.36)
(1.36)
08
CONSOLIDATED STATEMENT
OF FINANCIAL POSITION
Consolidated Statement of Financial Position
As at 30 June 2021
CURRENT ASSETS
Cash and cash equivalents
Inventory
Trade and other receivables
Prepayments
Disposal group classified as held for sale
Total Current Assets
NON-CURRENT ASSETS
Plant and equipment
Intangible assets and goodwill
Financial assets
Right-of-use assets
Total Non-Current Assets
TOTAL ASSETS
CURRENT LIABILITIES
Trade and other payables
Deferred revenue
Liabilities directly associated with disposal group
Financial liabilities at fair value through profit or loss
Lease liabilities - current
Total Current Liabilities
NON-CURRENT LIABILITIES
Provisions
Deferred income
Lease liabilities – non-current
Total Non-Current Liabilities
TOTAL LIABILITIES
NET ASSETS
EQUITY
Contributed equity
Share based payment reserve
Foreign currency translation reserve
Consolidation reserve
Accumulated losses
Equity attributable to equity holders of the parent
Non-controlling interest
TOTAL EQUITY
Note
8
9
10
4
11
12
20
14
13a)
13b)
4
15
14
13c)
14
16a)
16bi)
16bii)
30-Jun-21
$
5,433,241
872,444
2,348,634
546,576
280,475
9,481,370
5,272,202
7,048,880
564,186
1,869,006
14,754,274
24,235,644
1,796,235
-
89,659
4,034,763
209,433
6,130,090
-
2,506,281
1,773,374
4,279,655
10,409,745
13,825,899
84,511,983
7,490,483
212,381
(382,404)
(77,997,896)
13,834,547
(8,648)
13,825,899
The accompanying notes form part of these financial statements
30-Jun-20
$
1,873,373
402,237
521,684
71,032
362,657
3,230,983
2,192,974
-
673,740
1,831,377
4,698,091
7,929,074
2,705,818
100,440
109,254
-
53,924
2,969,436
19,982
-
1,845,300
1,865,282
4,834,718
3,094,356
60,149,457
5,380,904
85,284
(382,404)
(62,127,918)
3,105,323
(10,967)
3,094,356
31
09
CONSOLIDATED STATEMENT
OF CHANGES IN EQUITY
Consolidated Statement of Changes in Equity
For the year ended 30 June 2021
CONTRIBUTED
EQUITY
$
SHARE
BASED
PAYMENT
RESERVE
$
FOREIGN
CURRENCY
TRANSLATION
RESERVE
$
Balance at 1 July 2019
49,133,819 4,556,418
Other comprehensive income
Loss after income tax expense
Total comprehensive loss for
the year
Shares issued during the year (net
of share issue costs)
-
-
-
9,911,672
-
-
-
-
Transfer to issued capital
869,931
(869,931)
Share based payment
Acquisition of non-controlling
interest
-
1,694,417
234,035
-
Balance at 30 June 2020
60,149,457 5,380,904
Other comprehensive income
Loss after income tax expense
Total comprehensive loss for
the year
Shares issued during the year (net
of share issue costs)
Transfer to issued capital
Share based payment
Acquisition of business
(MedicaNL)
Unissued shares (MedicaNL)
Acquisition of business (MCC)
Equity issued to extinguish
financial liabilities
Conversion of convertible notes
Exercise of options
-
-
-
-
-
-
9,412,411
1,101,977
418,000
(418,000)
453,113
1,425,602
1,800,000
4,200,000
1,000,000
1,231,698
4,810,641
1,036,663
-
-
-
-
-
-
33,928
51,356
-
51,356
-
-
-
-
85,284
127,097
-
127,097
-
-
-
-
-
-
-
-
-
CONSOLIDATION
RESERVE
RETAINED
EARNINGS
NON-
CONTROLLING
INTEREST
TOTAL
$
-
-
-
-
-
-
-
(382,404)
$
$
$
(42,764,829)
(161,163)
10,798,173
-
-
51,356
(19,363,089)
(7,137) (19,370,226)
(19,363,089)
(7,137)
(19,318,870)
-
-
-
-
-
-
-
9,911,672
-
1,694,417
157,333
8,964
(382,404)
(62,127,918)
(10,967)
3,094,356
-
-
-
-
-
-
-
-
-
-
-
-
-
4,319
131,416
(15,869,978)
(2,000)
(15,871,978)
(15,869,978)
2,319 (15,740,562)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
10,514,388
-
1,878,715
1,800,000
4,200,000
1,000,000
1,231,698
4,810,641
1,036,663
Balance at 30 June 2021
84,511,983 7,490,483
212,381
(382,404) (477,997,896)
(8,648)
13,825,899
The accompanying notes form part of these financial statements
32
10
CONSOLIDATED STATEMENT
OF CASH FLOWS
Consolidated Statement of Cash Flows
For the year ended 30 June 2021
Cash flows from operating activities
Receipts from customers
Payments to suppliers and employees
Payments for research expenses
Research and development rebate / grants
Interest received
Interest paid
Income tax (paid) / received
Net cash used in operating activities
Cash flows from investing activities
Subsidiary disposed; net of cash disposed of
Acquisition of business; net of cash acquired (MCC)
Acquisition of business; net of cash acquired (MedicaNL)
Government grant received relating to plant and equipment
Proceeds from sales of plant and equipment
Loans to third parties
Proceeds from sale of investments
Purchase of plant and equipment / assets under construction
Net cash used in investing activities
Cash flows from financing activities
Proceeds from issue of shares and conversion of options
Proceeds from borrowings
Payment of lease liabilities
Transaction costs on issue of shares
Net cash provided by financing activities
Net increase / (decrease) in cash and cash equivalents held
Cash and cash equivalents at beginning of year
Foreign exchange movement in cash
Cash and cash equivalents at end of year
The accompanying notes form part of these financial statements
Note
30-Jun-21
$
30-Jun-20
$
2,162,812
(10,847,944)
(3,839,592)
507,248
7,984
(7,398)
27,278
2,072,246
(8,452,920)
(3,973,805)
518,952
14,242
(135,582)
-
(11,989,612)
(9,956,867)
5c
24
12
12
10
8
(79,687)
(400,000)
106,438
2,450,747
-
(546,995)
302,823
(3,327,105)
(1,493,779)
12,759,697
5,750,000
(255,993)
(1,202,646)
17,051,058
3,567,667
1,873,373
(7,799)
5,433,241
(13,252)
-
-
-
-
-
5,465
(962,097)
(969,884)
11,433,193
-
(183,611)
(787,677)
10,461,905
(464,846)
2,354,086
(15,867)
1,873,373
33
11
NOTES TO THE FINANCIAL
STATEMENTS
NOTES TO THE
FINANCIAL
STATEMENTS
34
Contents of the Notes
to the Financial Statements
1.
2.
3.
4.
5.
6.
7.
8.
9.
CORPORATE INFORMATION
SIGNIFICANT ACCOUNTING POLICIES
CRITICAL ACCOUNTING ESTIMATES AND JUDGEMENTS
DISPOSAL GROUP HELD FOR SALE AND DISCONTINUED OPERATIONS
REVENUE AND OTHER INCOME
COST OF SALES AND EXPENSES
INCOME TAX
CASH AND CASH EQUIVALENTS
INVENTORY
10. TRADE AND OTHER RECEIVABLES
11.
PLANT AND EQUIPMENT
12. BUSINESS COMBINATION
13. PAYABLES AND DEFERRED REVENUE
14.
15.
LEASES
FINANCIAL LIABILITIES AT FAIR VALUE THROUGH PROFIT OR LOSS
16. CONTRIBUTED EQUITY AND RESERVES
17. DIVIDENDS
18.
19.
20.
EARNINGS PER SHARE
FINANCIAL RISK MANAGEMENT
FAIR VALUE MEASUREMENT OF FINANCIAL INSTRUMENTS
21. CONTROLLED ENTITIES
22. SEGMENT REPORTING
23. CONTINGENCIES AND COMMITMENTS
24. CASH FLOW INFORMATION
25. AUDITOR’S REMUNERATION
26. PARENT COMPANY DISCLOSURES
27. RELATED PARTY TRANSACTIONS
28. SHARE BASED PAYMENTS
29. EVENTS AFTER THE REPORTING DATE
36
36
42
42
43
44
44
45
46
46
46
47
49
50
51
52
53
54
54
56
57
57
58
59
59
60
60
61
66
35
Notes to the Financial Statements
1. CORPORATE INFORMATION
The financial statements of MGC Pharmaceuticals Ltd for the year ended 30 June 2021 were authorised for issue in
accordance with a resolution of Directors on 29 September 2021. These consolidated financial statements and notes
represent those of MGC Pharmaceuticals Ltd (the “Company”) and Controlled Entities (the “consolidated group” or
“Group”). MGC Pharmaceuticals Ltd is a for-profit company limited by shares incorporated and domiciled in Australia
whose shares are publicly traded on the Australian Securities Exchange (“ASX”) and the main segment of the London
Stock Exchange (“LSE”). The registered office of the Company is 1202 Hay Street, West Perth WA 6005.
MGC Pharma is a European based bio-pharma company, specialising in the development and supply of standardised
phytomedicines to patients globally. It has three key clinical projects today, as well as a pipeline of further potential
therapies: CimetrA, a Phase 3 symptomatic treatment for early COVID-19, CannEpil, a Phase 2b cannabis-based therapy
for drug-resistant Epilepsy, and CogniCann, in a Phase 2 trial for symptomatic relief of Dementia. The Company currently
generates revenues from its ArtemiC range of products, and its cannabinoid products primarily distributed within
Australia, the UK, and South America.
2. SIGNIFICANT ACCOUNTING POLICIES
a) Statement of Compliance
The financial statements are general purpose financial statements that have been prepared in accordance with Australian
Accounting Standards, Australian Accounting Interpretations, other authoritative pronouncements of the Australian
Accounting Standards Board (“AASB”) and the Corporations Act 2001 as appropriate for ‘for-profit’ orientated entities.
Australian Accounting Standards set out accounting policies that the AASB has concluded would result in financial
statements containing relevant and reliable information about transactions, events and conditions. Compliance with
Australian Accounting Standards ensures that the financial statements and notes also comply with International Financial
Reporting Standards (“IFRS”) as issued by the International Accounting Standard Board (“IASB”). Material accounting
policies adopted in the preparation of these financial statements are presented below and they have been consistently
applied unless otherwise stated.
Basis of Preparation
The financial statements have been prepared on an accruals basis and are based on historical costs, modified, where
applicable, by the measurement at fair value of financial assets and liabilities.
The preparation of the financial statements requires the use of certain critical accounting estimates. It also requires
management to exercise its judgement in the process of applying the consolidated 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 3.
Financial report prepared on a going concern basis
The financial statements have been prepared on the going concern basis of accounting, which assumes the continuity of
normal business activities and the realisation of assets and settlement of liabilities in the ordinary course of business.
During the year ended 30 June 2021 the consolidated group incurred a loss from continuing operations of $15,409,341
(2020: $18,769,799) and net operating cash outflows of $11,989,612 (2020: $9,956,867). At 30 June 2021, the consolidated
group had a working capital surplus of $3,351,280 (2020: surplus $261,547), including a cash and cash equivalents
balance of $5,433,241 (2020: $1,873,373). Within the current liabilities are convertible notes which, under market
conditions at the date of this report are favourable for the holder to elect to convert to equity. There are $2,100,000 (face
value) of unredeemed convertible notes on issue at the date of this report.
The Group’s cashflow forecasts for the 12 months ending 30 September 2022 indicates that the Group will require
additional capital to meet its expenditure requirements and carry out its planned activities. Further to the recent listing
and oversubscribed capital raising on the London Stock Exchange, the Directors are satisfied that additional capital
can be raised as and when required to meet its current commitments and further planned activities , also noting that
the Group has not drawn down $9,250,000 of the existing convertible securities finance agreement (“the agreement”)
with Mercer Street Global Opportunity Fund, LLC (“the investor”). Any further drawdown is at the investor’s discretion,
and the Company having sufficient capacity under Chapter 7 of the ASX Listing Rules to issue the convertible notes, or
shareholder approval being obtained.
36
Based on the matters detailed above, the Directors are satisfied that the going concern basis of preparation is appropriate
and that the Group will be able to realise its assets and settle its obligations in the ordinary course of business over the
next 12 months.
The consolidated financial statements have been prepared on a going concern basis which contemplates continuity of
normal business activities and realisation of assets and settlement of liabilities in the normal course of business. In the
event that the Group is unable to obtain additional funding, there is significant uncertainty as to whether the Group will
be able to meet its debts as and when they fall due and thus continue as a going concern. The consolidated financial
statements do not include any adjustments relating to the recoverability and classification of the recorded asset amounts,
nor to the amounts or classification of liabilities that might be necessary should the Group not be able to continue as a
going concern.
b) Principles of Consolidation
The consolidated financial statements comprise the financial statements of MGC Pharmaceuticals Ltd and its
subsidiaries as at 30 June 2021 (“the Group”).
Control is achieved when the Group is exposed, or has rights, to variable returns from its involvement with the investee
and has the ability to affect those returns through its power over the investee. Specifically, the Group controls an investee
if and only if the Group has:
■ Power over the investee (i.e. existing rights that give it the current ability to direct the relevant activities of the investee);
■ Exposure, or rights, to variable returns from its involvement with the investee; and
■ The ability to use its power over the investee to affect its returns.
When the Group has less than a majority of the voting or similar rights of an investee, the Group considers all relevant
facts and circumstances in assessing whether it has power over an investee, including:
■ The contractual arrangement with the other vote holders of the investee;
■ Rights arising from other contractual arrangements; and
■ The Group’s voting rights and potential voting rights.
The Group re-assesses whether or not it controls an investee if facts and circumstances indicate that there are changes
to one or more of the three elements of control. Consolidation of a subsidiary begins when the Group obtains control over
the subsidiary and ceases when the Group loses control of the subsidiary. Assets, liabilities, income and expenses of a
subsidiary acquired or disposed of during the year are included in the statement of comprehensive income from the date
the Group gains control until the date the Group ceases to control the subsidiary.
Profit or loss and each component of other comprehensive income (“OCI”) are attributed to the equity holders of the
parent of the Group and to the non-controlling interests, even if this results in the non-controlling interests having a deficit
balance. When necessary, adjustments are made to the financial statements of subsidiaries to bring their accounting
policies into line with the Group’s accounting policies. All intra-group assets and liabilities, equity, income, expenses and
cash flows relating to transactions between members of the Group are eliminated in full on consolidation.
A change in the ownership interest of a subsidiary, without a loss of control, is accounted for as an equity transaction.
If the Group loses control over a subsidiary it, de-recognises the assets (including goodwill) and liabilities of the
subsidiary; de-recognises the carrying amount of any non-controlling interests; de-recognises the cumulative translation
differences recorded in equity; recognises the fair value of the consideration received; recognises the fair value of any
investment retained; recognises any surplus or deficit in profit or loss; and reclassifies the parent’s share of components
previously recognised in OCI to profit or loss or retained earnings, as appropriate, as would be required if the Group had
directly disposed of the related assets or liabilities.
The Group applies the acquisition method in accounting for business combinations. The cost of an acquisition is
measured as the aggregate of the consideration transferred, measured at acquisition date fair value and the amount of
any non-controlling interest (NCI) in the acquiree. Acquisition costs are expensed as incurred.
Goodwill is initially measured at cost being the excess of the aggregate of the consideration transferred and the amount
recognised for NCI over the fair value of the identifiable net assets acquired and liabilities assumed.
37
c) Foreign Currency
Functional and Presentation Currency
Items included in the financial statements of each of the Group’s entities are measured using the currency of the primary
economic environment in which the entity operates (“the functional currency”). The consolidated financial statements are
presented in Australian dollars, which is the Company’s functional and presentation currency.
Transactions and Balances
Foreign currency transactions are translated into the functional currency 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 period-end exchange rates of monetary assets and liabilities denominated in foreign currencies are
recognised in the statement of profit and loss and other comprehensive income, except when they are attributable to part
of the net investment in a foreign operation.
Foreign exchange gains and losses that relate to borrowings are presented in the statement of comprehensive income,
within finance costs. All other foreign exchange gains and losses are presented in the statement of profit or loss on a net
basis within other income or other expenses.
Non-monetary items that are measured at fair value in a foreign currency are translated using the exchange rates at the
date when the fair value was determined. Transaction differences on assets and liabilities carried at fair value are reported
as part of the fair value gain or loss.
Foreign operations
On consolidation, the assets and liabilities of foreign operations are translated into Australian dollars at the rate of
exchange prevailing at the reporting date and their statements of profit or loss are translated at exchange rates prevailing
at the dates of the transactions. The exchange differences arising on translation for consolidation purposes are
recognised in other comprehensive income. On disposal of a foreign operation, the component of other comprehensive
income relating to that particular foreign operation is recognised in profit or loss.
Any goodwill arising on the acquisition of a foreign operation and any fair value adjustments to the carrying amounts of
assets and liabilities arising on the acquisition are treated as assets and liabilities of the foreign operation and translated
at the spot rate of exchange at the reporting date.
d) Trade Receivables and Other Short Term Debtors
Trade receivables and other short term debtors are all classified as financial assets held at amortised cost on the basis
they are held with the objective of collecting contractual cash flows and the cash flows relate to payments of principal and
interest on the principal amount outstanding.
The Group applies the simplified approach in measuring expected credit losses (ECLs) for trade receivables and other
short-term debtors, whereby an allowance for impairment is considered across all trade receivables and other short-
term debtors, regardless of whether a credit event has occurred, based on the expected losses over the lifetime of the
receivable. Therefore, the Group does not track changes in credit risk but instead recognises a loss allowance based
on lifetime ECLs at each reporting date. The Group’s exposure to bad debts is not significant and default rates have
historically been very low. Trade and other short term receivables are written off when there is no reasonable expectation
of recovery, which may be indicated by the debtor failing to engage in a payment plan or the debtor failing to make timely
contractual payments.
e) Other Financial Assets
Other financial assets are initially measured at fair value. Transaction costs are included as part of the initial
measurement, except for financial assets at fair value through profit or loss. Other financial assets are subsequently
measured at either amortised cost or fair value depending on their classification. Classification is determined based on
both the business model within which such assets are held and the contractual cash flow characteristics of the financial
asset unless, an accounting mismatch is being avoided.
Financial assets are derecognised when the rights to receive cash flows have expired or have been transferred and the
consolidated entity had transferred substantially all the risks and rewards of ownership. When there is no reasonable
expectation of recovering part, or all, of a financial asset, it’s carrying value is written off.
Financial assets at fair value through profit or loss
Financial assets not measured at amortised cost or at fair value through other comprehensive income are classified as
financial assets at fair value through profit or loss. Typically, such financial assets will be either: (i) held for trading, where
they are acquired for the purpose of selling in the short-term with an intention of making a profit, or a derivative; or
(ii) designated as such upon initial recognition where permitted. Fair value movements are recognised in profit or loss.
38
f) Impairment of Non-Financial Assets
Non-financial assets are tested for impairment when there is an indication that the asset may be impaired (which is
assessed at least each reporting date).Impairment exists when the carrying value of an asset or cash generating unit
exceeds its recoverable amount, which is the higher of its fair value less costs of disposal and its value in use. Fair value
less costs of disposal calculations are based on available data from binding sales transactions, conducted at arm’s length,
for similar assets or observable market prices less incremental costs of disposing of the asset. Value in use calculations
are based on a discounted cash flow (“DCF’) model, where relevant. The cash flows are derived from the budget for the
next five years and do not include restructuring activities that the Group is not yet committed to or significant future
investments that will enhance the performance of the assets of the CGU being tested.
g) Current and Non-Current Classification
The Group presents assets and liabilities in the statement of financial position based on current/non-current
classification. An asset is current when it is:
■ Expected to be realised or intended to be sold or consumed in the normal operating cycle;
■ Held primarily for the purpose of trading;
■ Expected to be realised within twelve months after the reporting period; or
■ A Cash or cash equivalent unless restricted from being exchanged or used to settle a liability for at least twelve months
after the reporting period.
All other assets are classified as non-current. A liability is current when it is:
■ Expected to be settled in normal operating cycle;
■ Held primarily for the purpose of trading;
■
It is due to be settled within twelve months after the reporting period; or
■ There is no unconditional right to defer the settlement of the liability for at least twelve months after the reporting
period.
The Group classifies all other liabilities as non-current.
Deferred tax assets and liabilities are classified as non-current assets and liabilities.
h) Government Grants
Government grants are recognised when there is a reasonable assurance that the grant will be received and all attached
conditions will be compiled with. When the grant relates to an expense item, it is recognised as income on a systematic
basis over the periods that the costs, which it is intended to compensate, are expensed. When the grant relates to an
asset, it is recognised as income in equal amounts over the expected useful life of the related asset.
i) 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 Tax Office. In these circumstances the GST is recognised as part of the cost of
acquisition of the asset, or as part of an item of the expense. Receivables and payables in the statement of financial
position are shown inclusive of GST.
Cash flows are presented in the consolidated statement of cash flows on a gross basis, except for the GST component of
investing and financing activities, which are disclosed as operating cash flows.
j) Leases
Group as Lessee
The Group assesses at contract inception whether a contract is, or contains, a lease. That is, if the contract conveys the
right to control the use of an identified asset for a period of time in exchange for consideration.
Right-of-use assets
The Group recognises right-of-use assets at the commencement date of the lease (i.e. the date the underlying asset is
available for use). Right-of-use assets are measured at cost, less any accumulated depreciation and impairment losses,
and adjusted for any remeasurement of lease liabilities. The cost of right-of-use assets includes the amount of lease
liabilities recognised, initial direct costs incurred, and lease payments made at or before the commencement date less
any lease incentives received. Unless the Group is reasonably certain to obtain ownership of the leased asset at the end of
the lease term, the recognised right-of-use assets are depreciated on a straight-line basis over the shorter of its estimated
useful life and the lease term. Right-of-use assets are subject to impairment.
39
Lease liabilities
At the commencement date of the lease, the Group recognises lease liabilities measured at the present value of lease
payments to be made over the lease term. The lease payments include fixed payments (including in substance fixed
payments) less any lease incentives receivable, variable lease payments that depend on an index or a rate, and amounts
expected to be paid under residual value guarantees. The lease payments also include the exercise price of a purchase
option reasonably certain to be exercised by the Group and payments of penalties for terminating a lease, if the lease term
reflects the Group exercising the option to terminate. The variable lease payments that do not depend on an index or a rate
are recognised as expense in the period on which the event or condition that triggers the payment occurs. In calculating
the present value of lease payments, the Group uses the incremental borrowing rate at the lease commencement date
if the interest rate implicit in the lease is not readily determinable. After the commencement date, the amount of lease
liabilities is increased to reflect the accretion of interest and reduced for the lease payments made. In addition, the
carrying amount of lease liabilities is remeasured if there is a modification, a change in the lease term, a change in the
in-substance fixed lease payments or a change in the assessment to purchase the underlying asset.
Short-term leases and leases of low-value assets
The Group applies the short-term lease recognition exemption to its short-term leases of office rental (i.e. those leases
that have a lease term of 12 months or less from the commencement date and do not contain a purchase option). It also
applies the lease of low-value assets recognition exemption to leases of office equipment that are considered of low
value. Lease payments on short-term leases and leases of low-value assets are recognised as expense on a straight-line
basis over the lease term.
k) Other significant accounting policies
Refer to the relevant notes to the financial statements for other accounting policies, including revenue (note 5), income
taxes (note 7), government grants (note 5), cash and cash equivalents (note 8) inventory (note 9), plant and equipment
(note 11), share-based payments (note 28) and employee benefits (note 13).
l) Rounding of Amounts
The Company is a kind referred to in Legislative Instrument 2016/191 issued by the Australian Securities and Investment
Commission, relating to the “rounding off” of amounts in the financial statements. Amounts in the financial statements
have been rounded off in accordance with that class order to the nearest dollar.
New and amended Accounting Standards and Interpretations adopted by the Group
The Group has adopted all of the new and revised Accounting Standards and Interpretations issued by the Australian
Accounting Standards Board (the AASB) that are relevant to its operations and effective from 1 July 2020, with no material
impact to the Group.
The Group has not early adopted any new or amended Accounting Standards or Interpretations issued but not yet
effective, the impacts of which are not expected to be material to the Group, as follows:
REFERENCE
AASB 2020-3 Amendment to
AASB 9 – Fees in the ‘10 per
cent’ Test for Derecognition of
Financial Liabilities
DESCRIPTION
The application of this Standard is effective from 1 January 2022 and will be adopted by the Group
on 1 July 2022. Under AASB 9, an existing financial liability that has been modified or exchanged is
considered extinguished when the contractual terms of the new liability are substantially different,
measured by the “10 per cent” test. That is, when the present value of the cash flows under the new
terms, including any fees paid or received, is at least 10 per cent different from the present value of the
remaining cash flows of the original financial liability.
The amendment to AASB 9 clarifies that fees included in the 10 per cent test are limited to fees paid
or received between the borrower and the lender, including amounts paid or received by them on the
other’s behalf. When assessing the significance of any difference between the new and old contractual
terms, only the changes in contractual cash flows between the lender and borrower are relevant.
Consequently, fees incurred on the modification or exchange of a financial liability paid to third parties
are excluded from the 10 per cent test.
The application of this Standard is effective from 1 January 2022 and will be adopted by the Group
on 1 July 2022. The amendments to AASB 10 Consolidated Financial Statements and AASB 128
Investments in Associates and Joint Ventures clarify that a full gain or loss is recognised when a
transfer to an associate or joint venture involves a business as defined in AASB 3. Any gain or loss
resulting from the sale or contribution of assets that does not constitute a business, however, is
recognised only to the extent of unrelated investors’ interests in the associate or joint venture.
AASB 2014-10 Amendments
to AASs – Sale or Contribution
of Assets between an Investor
and its Associate or Joint
Venture
40
REFERENCE
AASB 2021-5 Amendments to
AASs – Deferred Tax related to
Assets and Liabilities arising
from a Single Transaction
AASB 2020-3 Amendments
to AASB 3 – Reference to the
Conceptual Framework
AASB 2020-1 Amendments
to AASs – Classification of
Liabilities as Current or
Non-current
AASB 2021-2 Amendments to
AASB 7, AASB 101, AASB 134
Interim Financial Reporting
and AASB Practice Statement
2 Making Materiality
Judgements – Disclosure
of Accounting Policies
AASB 2020-3 Amendments
to AASB 116 – Property, Plant
and Equipment: Proceeds
before Intended Use
DESCRIPTION
The application of this Standard is effective from 1 January 2023 and will be adopted by the Group on
1 July 2023. The amendment clarify the deferred tax accounting on potential exceptions that may or
may not apply. It requires entities to also recognise deferred tax for all temporary differences related to
leases, decommissioning, restoration and similar liabilities at the beginning of the earliest comparative
period presented.
The application of this Standard is effective from 1 January 2022 and will be adopted by the Group
on 1 July 2022. The IASB’s assessment of applying the revised definitions of assets and liabilities
in the Conceptual Framework to business combinations showed that the problem of day 2 gains or
losses would be significant only for liabilities that an acquirer accounts for after the acquisition date
by applying IAS 37 Provisions, Contingent Liabilities and Contingent Assets or IFRIC 21 Levies. The
Board updated IFRS 3 in May 2020 for the revised definitions of an asset and a liability and excluded
the application of the Conceptual Framework to liabilities and contingent liabilities within the scope of
IAS 37 or IFRIC 21.
The application of this amendment is effective from 1 January 2023 and will be adopted by the Group
on 1 July 2023. A liability is classified as current if the entity has no right at the end of the reporting
period to defer settlement for at least 12 months after the reporting period. The AASB recently issued
amendments to AASB 101 Presentation of Financial Statements to clarify the requirements for
classifying liabilities as current or non-current. Specifically:
■ The amendments specify that the conditions which exist at the end of the reporting period are
those which will be used to determine if a right to defer settlement of a liability exists.
■ Management intention or expectation does not affect classification of liabilities.
In cases where an instrument with a conversion option is classified as a liability, the transfer of equity
instruments would constitute settlement of the liability for the purpose of classifying it as current or
non-current.
The application of this amendment is effective from 1 January 2023 and will be adopted by the
Group on 1 July 2023. The amendments to AASB 101 require disclosure of material accounting policy
information, instead of significant accounting policies. Unlike ‘material’, ‘significant’ was not defined
in Australian Accounting Standards. Leveraging the existing definition of material with additional
guidance is expected to help preparers make more effective accounting policy disclosures. The
guidance illustrates circumstances where an entity is likely to consider accounting policy information
to be material. Entity-specific accounting policy information is emphasised as being more useful than
generic information or summaries of the requirements of Australian Accounting Standards.
The application of this amendment is effective from 1 January 2022 and will be adopted by the Group
on 1 July 2022. Under AASB 116 Property, Plant and Equipment, net proceeds from selling items
produced while constructing an item of property, plant and equipment12 are deducted from the cost of
the asset. The IASB’s research indicated practical diversity in interpreting this requirement. As a result,
AASB 116 was amended to prohibit an entity from deducting from the cost of an item of property, plant
and equipment, the proceeds from selling items produced before that asset is available for use.
An entity is also required to measure production costs of the sold items by applying AASB 102
Inventories. Proceeds from selling any such items, and the cost of those items, are recognised in profit
or loss in accordance with applicable standards.
41
3. CRITICAL ACCOUNTING ESTIMATES AND JUDGEMENTS
The Directors evaluate estimates and judgements incorporated into the financial report based on historical knowledge and
best available current information. Estimates assume a reasonable expectation of future events and are based on current
trends and economic data, obtained both externally and within the Group. Judgements and estimates which are material
to the financial report are found at the following notes:
a) Share Based Payments (refer note 28).
b) Valuation of financial liabilities valued at fair value through profit or loss (refer note 15).
c) Leases (refer note 14).
d) Research and Development Rebate (refer note 5c).
e) Impairment Assessment of Non-Current Assets (refer note 11).
f) Expected Credit Losses (refer note 10).
4. DISPOSAL GROUP HELD FOR SALE AND DISCONTINUED OPERATIONS
During June 2020, MGC Pharma signed an agreement to sell its 100% interest in subsidiary MGC Nutraceuticals to a
US OTC publicly traded company, Onassis Holdings Corp. (OTC: “ONSS”). The transaction has been delayed however is
expected to be completed in the latter part of 2021. The transaction will complete upon ONSS conducting an IPO, of which
MGC Pharma will receive shares to the value of US $6,000,000.
MGC Nutraceuticals d.o.o has been classified as a disposal group held for sale and as a discontinued operation,
with results below:
Revenue
Expenses
Pre-tax loss
Income tax expense/benefit
Assets and liabilities of MGC Nutraceuticals d.o.o classified as held for sale:
Non-current assets classified as held for sale
Cash and cash equivalents
Trade and other debtors
Inventory
Liabilities directly associated with non-current assets classified held for sale
Trade and other payables
Deferred revenue
Net assets of disposal group
30-Jun-21
33,156
(495,793)
(462,637)
-
30-Jun-20
148,544
(748,971)
(600,427)
-
30-Jun-21
$
30-Jun-20
$
79,687
200,788
-
280,475
26,269
63,390
89,659
190,816
13,252
155,640
193,765
362,657
43,841
65,413
109,254
253,403
42
5. REVENUE AND OTHER INCOME
Revenue from contracts with customers
Revenue is recognised at an amount that reflects the consideration to which the consolidated entity is expected to be
entitled in exchange for transferring goods or services to a customer. For each contract with a customer, the consolidated
entity: identifies the contract with a customer; identifies the performance obligations in the contract; determines the
transaction price which takes into account estimates of variable consideration and the time value of money; allocates the
transaction price to the separate performance obligations on the basis of the relative stand-alone selling price of each
distinct good or service to be delivered; and recognises revenue when or as each performance obligation is satisfied in a
manner that depicts the transfer to the customer of the goods or services promised.
Variable consideration within the transaction price, if any, reflects concessions provided to the customer such as
discounts, rebates and refunds, any potential bonuses receivable from the customer and any other contingent events.
Such estimates are determined using either the ‘expected value’ or ‘most likely amount’ method. The measurement
of variable consideration is subject to a constraining principle whereby revenue will only be recognised to the extent
that it is highly probable that a significant reversal in the amount of cumulative revenue recognised will not occur. The
measurement constraint continues until the uncertainty associated with the variable consideration is subsequently
resolved. Amounts received that are subject to the constraining principle are initially recognised as deferred revenue in the
form of a separate refund liability.
Revenue from sale of pharma products
Revenue from the sale of cannabinoids is recognised when the goods have been delivered, at which point the customer
obtains control of the goods. In most cases, sales are B2B with revenue recognised as they are delivered to the pharmacy.
Revenue from consulting services
Revenue from providing clinical research services are recognized over time as the performance obligations are satisfied.
Revenue from sale of non-pharma products
Revenue from the sales of cosmetics is recorded when the products have been delivered to the consumer, signifying
transfer of ownership and the point the customer obtains control of the goods.
Interest revenue
Interest revenue is recognized using the effective interest rate method.
a) Revenue from contracts with customers
Pharma sales
Consulting services (clinical research fees and clinic consults)
Non-pharma sales
b) Finance income
Interest income calculated using the effective interest rate method
c) Other operating income
Refund on research and development claim1
Government grants received
30-Jun-21
$
2,726,075
236,822
-
2,962,897
7,632
7,632
507,248
99,497
606,745
30-Jun-20
$
1,197,130
-
882,039
2,079,169
12,336
12,336
429,401
89,450
518,851
1. During the year ended 30 June 2021, the Group received a research and development rebate following lodgement of a
claim for its financial year ended 30 June 2020.
Research and development rebates are accounted for as a government grant. Management judgement is required
to assess that the rebate meets the recognition criteria and in determining the measurement of the rebate including
the assessment of the eligibility and appropriateness of the apportionment of eligible expenses based on research
and development activities undertaken by the consolidated entity and taking into consideration relevant legislative
requirements.
Further, the Research and Development rebate program in Australia is a self-assessment regime and there is a
four-year period from the date of lodgement where the claim may be subject to a review by the Australian Taxation Office
or AusIndustry, with any amounts over-claimed being potentially subject to full repayment with interest and penalties.
43
6. COST OF SALES AND EXPENSES
a) Cost of sales
Cost of goods sold - Pharma
Cost of sales – Consulting services
Cost of goods sold – Non-pharma
b) Administrative expenses
Corporate costs
Professional and consultancy fees
Directors’ fees
Employee benefit expenses
Employee share based payment expense
Travel expenses
Marketing expenses
Depreciation
Office and administrative expenses
c) Other operating expenses
Unrealised foreign exchange
Realised foreign exchange
Inventory write-off
Laboratory operation expenses
Research expense
d) Impairment expense
Write off/impairment of intangible assets
e) Finance cost
Finance costs
30-Jun-21
$
1,482,535
169,950
-
1,652,485
511,705
1,483,060
871,804
1,867,248
1,647,715
309,272
583,185
491,408
522,467
8,287,864
(44,386)
74,400
128,210
3,194,687
1,897,779
5,250,690
-
-
369,135
369,135
30-Jun-20
$
1,242,311
-
662,193
1,904,504
303,681
1,034,810
1,178,114
1,270,134
854,915
399,934
562,125
481,130
524,304
6,609,147
69,896
80,506
-
3,285,946
2,084,208
5,520,556
5,117,767
5,117,767
135,582
135,582
7. INCOME TAX
The income tax expense/(benefit) for the period is the tax payable on the current period’s taxable income based on the
applicable income tax rate for each jurisdiction adjusted by changes in the deferred tax assets and liabilities attributable to
temporary differences and to unused tax losses.
The current income tax charge is calculated on the basis of the tax laws enacted or substantively enacted at the end of the
reporting period in the countries where the company’s subsidiaries and associates operate and generate taxable income.
Deferred income tax is provided on all temporary differences at the statement of financial position date, arising between
the tax bases of assets and liabilities and their carrying amounts in the consolidated financial statements, and are
recognised for all taxable temporary differences,
■ Except where the deferred income tax liability arises from the initial recognition of an asset or liability in a transaction
that is not a business combination and, at the time of the transaction, affects neither the accounting profit nor taxable
profit or loss; and
■
In respect of taxable temporary differences associated with investments in subsidiaries, associates and interests in
joint ventures, except where the timing of the reversal of the temporary differences can be controlled and it is probable
that the temporary differences will not reverse in the foreseeable future.
44
Deferred income tax assets are recognised for all deductible temporary differences, the carry-forward of unused tax
credits and unused tax losses. Deferred tax assets are recognised to the extent that it is probable that taxable profit will be
available against which the deductible temporary differences, and the carry forward of unused tax credits and unused tax
losses can be utilised:
■ Except where the deferred income tax asset relating to the deductible temporary difference arises from the initial
recognition of an asset or liability in a transaction that is not a business combination and, at the time of the transaction,
affects neither the accounting profit nor the taxable profit or loss; and
■
In respect of taxable temporary differences associated with investments in subsidiaries, associates and interests and
joint ventures, deferred tax assets are only recognised to the extent that it is probable that the temporary differences
will reverse in the foreseeable future extent that it is probable that the temporary differences can be utilised.
Deferred income tax assets and liabilities are measured at the tax rates that are expected to apply to the year when
the asset is realised or the liability is settled, based on tax rates (and tax laws) that have been enacted or substantively
enacted at the statement of financial position date.
Income taxes relating to items recognised directly in equity are recognised in equity and not in the statement of profit or
loss and other comprehensive income.
Tax Consolidation
The Company and its wholly-owned Australian subsidiaries have formed an income tax consolidated group under the tax
consolidated legislation. Each entity in the Group recognises its own current and deferred tax assets and liabilities. Such
taxes are measured using the ‘stand-alone taxpayer’ approach to allocation. The Group notified the Australian Taxation
Office that it had formed an income tax consolidated group to apply from 21 October 2005. The tax consolidated group
has entered a tax funding agreement whereby each company in the Group contributes to the income tax payable by the
Group in proportion to their contributions to the Group’s taxable income.
The Group has carried forward tax losses which have not been recognised as deferred tax assets as it is not considered
sufficiently probable that these losses will be recouped by means of future profits taxable in the relevant jurisdictions.
a) Major components of income tax expense for the periods presented:
Current tax
Deferred tax
Income tax expense / (benefit) reported in the Statement of Comprehensive Income
b) The prima facie tax on (loss) from continuing operations and discontinued operations
before income tax is reconciled to the income tax as follows:
Prima facie tax payable on (loss) from continuing operations and discontinued operations
before income tax at 26% (2020: 27.5%)
Adjustments due to permanent differences
Deferred tax assets not brought to account
Under/over provision of prior year
Income tax expense/(benefit)
30-Jun-21
$
(27,278)
-
(27,278)
(4,141,448)
2,004,491
2,136,957
(27,278)
(27,278)
30-Jun-20
$
-
-
-
(5,326,812)
483,339
2,732,232
-
-
Deferred Tax Assets Not Brought to Account, the benefits of which will only be realised if the
conditions for deductibility set out in note above
Tax Losses
Temporary Differences
Total
6,837,338
513,223
7,350,561
6,164,503
428,686
6,593,189
8. CASH AND CASH EQUIVALENTS
For the purpose of presentation in the statement of cash flows, cash and cash equivalents includes cash on hand,
deposits held at call with financial institutions, other short-term, highly liquid investments with original maturities of three
months or less that are readily convertible to known amounts of cash and which are subject to an insignificant risk of
changes in value, and bank overdrafts.
Cash at bank
30-Jun-21
$
5,433,241
5,433,241
30-Jun-20
$
1,873,373
1,873,373
45
9. INVENTORY
Inventories are stated at the lower of cost and net realisable value. Costs of inventories are determined on a first-in-first-
out basis. Net realisable value represents the estimated selling price for inventories less all estimated costs of completion
and costs necessary to make the sale.
Inventories
Raw materials
Work in progress
30-Jun-21
$
300,834
571,610
-
872,444
30-Jun-20
$
92,511
290,940
18,786
402,237
10. TRADE AND OTHER RECEIVABLES
Trade receivables are generally due for settlement between thirty (30) and ninety (90) days from the date of recognition.
They are presented as current assets unless collection is not expected for more than 12 months after reporting date.
Current
Trade receivables
Expected credit loss on trade receivables
Other receivables
GST/VAT receivable
Short term loan to third party
Financial asset at fair value through profit or loss1
Other receivables are non-interest bearing and are generally on terms of 30 days.
1. Financial asset at fair value through profit or loss
Opening - financial asset at fair value through profit or loss
Loans advanced to third parties
Fair value loss on financial assets
Closing – financial asset at fair value through profit or loss
30-Jun-21
$
890,299
(49,340)
818,784
688,891
-
-
2,348,634
30-Jun-21
$
-
546,995
(546,995)
-
30-Jun-20
$
-
-
214,209
254,297
53,178
-
521,684
30-Jun-20
$
-
-
-
-
During the year, funds were loaned to an unrelated entity to advance registration of its phytomedicine products in Russia
and CIS countries, interest-bearing and repayable in 24 months. MGC Pharma is party to a draft agreement to acquire a
54% interest in this entity for nominal consideration, with finalisation of the transaction subject to signing and physical
lodgement of the share transfer document in the country of incorporation, expected to occur in the coming months.
The loan has been classified as a financial asset at fair value through profit or loss, with a fair value determined to be nil
at 30 June 2021 due to the equity risk associated with the loan.
11. PLANT AND EQUIPMENT
Plant and equipment are stated at historical cost less accumulated depreciation and impairment. Historical cost includes
expenditure that is directly attributable to the acquisition of the items.
Depreciation is calculated on a straight-line basis to write off the net cost of each item of plant and equipment over their
expected useful lives as follows:
Plant and equipment
3-5 years
The residual values, useful lives and depreciation methods are reviewed, and adjusted if appropriate, at each reporting
date.
An item of property, plant and equipment is derecognised upon disposal or when there is no future economic benefit
to the Group. Gains and losses between the carrying amount and the disposal proceeds are taken to profit or loss.
Any revaluation surplus reserve relating to the item disposed of is transferred directly to retained profits.
46
During the period, the Group signed a contract with BioPharmax to complete construction on a fully functioning GMP
certified manufacturing facility in Malta for liquid dose form product and the anti-inflammatory product, ArtemiC™.
Construction of the facility, in progress at 30 June 2021, is 80% funded by way of grant from Malta Enterprises (refer to
note 13c).
Plant and equipment*
- gross carrying amount at cost
- accumulated depreciation
Construction in progress
- gross carrying amount at cost
- accumulated depreciation
30-Jun-21
$
1,938,890
(1,105,797)
833,093
4,439,109
-
4,439,109
30-Jun-20
$
1,964,672
(905,455)
1,059,217
1,133,757
-
1,133,757
Total property, plant and equipment
* Plant and equipment primarily comprises laboratory fixtures and fittings and equipment.
5,272,202
2,192,974
Property, plant and equipment movement
Opening balance at 1 July
Additions
Disposal
Depreciation
Foreign currency translation
Impairment testing
30-Jun-21
$
2,192,974
3,538,808
(68,417)
(340,024)
(51,139)
5,272,202
30-Jun-20
$
1,470,479
1,120,963
(28,830)
(320,943)
(48,695)
2,192,974
Slovenia
The Group did not identify any indicators of impairment in relation to the Slovenia CGU, primarily the GMP laboratory.
Malta
The Group’s plant and equipment balance in Malta consisted of construction in progress, relating to design and
engineering work for its planned Malta operations. The temporary delay in the larger project as disclosed in note 14 was
identified as an impairment trigger for the balances associated with that project. The Group determined based on a
value-in-use discounted cash flow model using its internally developed feasibility estimates for the project, a discount rate
of 20%, and commencement of construction assumed in 2022, that no impairment existed in relation to the carrying value
of construction in progress associated with this site of $1,097,670 at 30 June 2021, or the associated right-of-use asset.
12. BUSINESS COMBINATION
Medicinal Cannabis Clinics (MCC)
On 23 November 2020 MGC Pharma completed the acquisition of the business of an operating telehealth clinic,
Medicinal Cannabis Clinics (MCC). Alongside revenue generated from consults, this acquisition provides MGC Pharma
with an operating platform with direct access to patients, along with a distribution agreement with Cannvalate, the
current operator of the clinic. The acquisition also allows the Group to continue providing its high-quality GMP certified
medications to patients in Australia and further improves profit margins while keeping its products at the current
competitive prices. A new wholly owned subsidiary, Medicinal Cannabis Clinics Pty Ltd, has been incorporated to acquire
the MCC business.
The total purchase consideration for the business was $1,400,000, comprising $400,000 in cash and $1,000,000 in
ordinary shares (45,454,545 shares issued at a fair value of $0.022 per share on the date of issue).
47
The assets recognised as a result of the acquisition are as follows:
Provisional goodwill
Net identifiable assets acquired
Fair value
$
1,400,000
1,400,000
The fair value of the acquired Goodwill is provisional as the Group has not yet obtained valuations for any separately
identifiable intangibles acquired.
MediCaNL Israel 2019 Ltd (MediCaNL)
On 21 April 2021, MGC Pharma completed the 100% acquisition of MedicaNL Israel 2019 Ltd (MedicaNL), an Israeli
company operating and providing specialist services to the pharmaceutical sector for development of new medicines.
The acquisition will enable MGC Pharma bring inhouse and speed up its pipeline of clinical trials, which will delivery long
term cost savings to the Group. The consideration for the transaction amounted to $6,000,000 calculated using a 10-day
VWAP prior to the acquisition date. The consideration shares are to be issued in tranches, as follows;
■ 30% due upon completion (issued 10 May, refer note 16);
■ 20% on the date which is 4 months from the date of settlement;
■ 20% on the date which is 7 months from the date of settlement;
■ 20% on the date which is 10 months from the date of settlement; and
■ 10% on the date which is 13 months from the date of settlement
Details of the acquisition are as follows:
Cash and cash equivalents
Trade and other receivables
Trade and other payables
Net assets acquired
Provisional goodwill
Net identifiable assets acquired
Representing;
Consideration paid at 30 June 2021
Unissued shares
Provisional fair value
$
106,438
415,781
(171,099)
351,120
5,648,880
6,000,000
1,800,000
4,200,000
6,000,000
The fair value of the acquired assets are provisional as the Group has not yet obtained valuations for any separately
identifiable intangibles acquired.
Goodwill
Opening balance at 1 July
- write-off/provision for impairment
- Goodwill on acquisition of Medicinal Cannabis Clinics
- Goodwill on acquisition of MedicaNL
- Foreign currency translation
30-Jun-21
$
-
-
1,400,000
5,648,880
-
7,048,880
30-Jun-20
$
5,034,309
(5,038,064)
-
-
3,755
-
The provisional goodwill arising from the Group’s current period acquisitions is not yet at a stage to be reliably determined
or allocated to cash generating units. The Group assessed that there were no impairment triggers in relation to the
unallocated provisional goodwill at 30 June 2021.
48
13. PAYABLES AND DEFERRED REVENUE
These amounts represent liabilities for goods and services provided to the Group prior to the end of the financial year,
which remain unpaid at year end. The amounts are unsecured and are usually paid within 60 days of recognition. They are
recognised at fair value on initial recognition and subsequently measured at amortised cost, using the effective interest
rate method.
Liabilities for wages and salaries, including non-monetary benefits, annual leave and accumulating sick leave expected
to be settled within 12 months after the period end in which the employees render the related service are recognised in
respect of employees’ services up to the end of the reporting period and are measured at the amounts expected to be
paid when the liabilities are settled. The liability for annual leave and accumulating sick leave is recognised in the provision
for employee benefits. All other short-term employee benefit obligations are presented as payables.
a) Current trade and other payables
Trade payables
Accruals
Other payables
b) Deferred revenue
Deferred revenues - current
30-Jun-21
$
1,222,143
380,770
193,322
1,796,235
-
-
30-Jun-20
$
2,003,677
556,205
145,936
2,705,818
100,440
100,440
Deferred revenue represents the Group’s obligation to transfer goods or services to a customer for which the Group has
received consideration at 30 June 2021.
Refer to note 19 for details on management of financial risk.
c) Deferred Income
Non-Current
Deferred income - Malta grant*
Closing balance
30-Jun-21
$
2,506,281
2,506,281
30-Jun-20
$
-
-
* During the year, the Group received approval for a grant from Malta Enterprises to cover 80% of the construction costs of
a production facility, to the value of €3,073,000 ($4,925,000). As at 30 June, an amount of $2,506,281 had been received
from Malta Enterprise. In accordance with AASB 120, the grant will be recognised as income on a systematic basis over
the useful life of the building once completed. Under the conditions of the grant, the Group was to complete construction
of the facility within 6 months of 10 December 2020 and, should the Group cease operations in Malta within five years
from the start of operations, Malta Enterprise retains the right to take possession of assets funded through the grant. In
March 2021 the Group received approval from Malta Enterprise to extend the period for completion of construction to
October 2021.
49
14. LEASES
At reporting date the Group has two long-term leases for the use of the land for the construction of facilities in Malta – a
65 year lease entered into in the prior period for the larger site and a 5 year lease entered into the current period for the
construction of the ArtemiC production facility. The Group also has leases for office and lab rental.
Below are the carrying amounts of right-of-use assets recognised for the period:
Right-of-use assets
Opening balance at 1 July
Additions of right-of-use assets in period
Depreciation of right-of-use assets
Closing balance
Below are the carrying amounts of lease liabilities for the period:
Lease liabilities
Opening balance at 1 July
Additions to lease liabilities
Interest on lease liabilities
Lease payments
Closing balance
Current
Non-current
Total lease liability
30-Jun-21
$
1,831,377
189,013
(151,384)
1,869,006
30-Jun-21
$
1,899,224
189,013
150,563
(255,993)
1,982,807
209,433
1,773,374
1,982,807
30-Jun-20
$
185,908
1,805,656
(160,187)
1,831,377
30-Jun-20
$
185,908
1,805,656
130,637
(222,977)
1,899,224
53,924
1,845,300
1,899,224
The following amounts were recognised in the consolidated statement of profit or loss and comprehensive income for the
period:
Depreciation on right-of-use asset
Interest expense on lease liabilities
Expense related to short-term leases
Total amounts recognised in profit or loss
The following are amounts recognised in the consolidated statement of cash flows:
Total cash outflows for leases
30-Jun-21
$
151,384
150,563
62,771
364,718
30-Jun-21
$
318,764
30-Jun-20
$
160,187
130,637
183,611
474,435
30-Jun-20
$
406,588
Malta long-term lease agreement
Refer to note 23 for disclosures relating to additional commitments on the Malta leases.
To the extent that the conditions under the lease agreement for the larger site are not met, including the condition
requiring commencement of construction on the site within three months of the date of the necessary approvals being
received, being 8 August 2019, the lessor may issue a notice of breach, 30 days after which it may elect to begin imposing
a penalty of EUR 12,000 per day that the breach persists, or may at its discretion terminate the lease agreement. Due
to changing circumstances arising from the COVID-19 pandemic, the Group prioritised construction of a smaller facility
in Malta for the production of ArtemiC (for which government grant assistance was received as disclosed in Note 13),
and delayed construction of the larger facility. It is anticipated commencement of this construction will not occur until
GMP certification of the current facility in construction, anticipated in mid-late 2022. At 30 June 2021, and to the date of
this report, the Group has not received a notice of breach from the lessor and has had communications with the lessor
supportive of MGC Pharma’s plans.
50
15. FINANCIAL LIABILITIES AT FAIR VALUE THROUGH PROFIT OR LOSS
In September 2020, the Company entered into a convertible note financing facility with Mercer Street Global Opportunity
Fund (Mercer), under which up to $15,000,000 can be drawn down in exchange for the issue of a number of convertible
notes with a face value of $1.00 each equal to 110% of the amount of funding received. The notes are repayable at
face value 12 months from the date of the respective draw down, if not converted or repurchased prior to maturity.
Following the initial tranche of $2,250,000 funding received (Tranche 1 as described below), further drawdowns under the
agreement are subject to the discretion of both the Company and Mercer. Upon commencement of the facility, ordinary
shares to the value of $225,000 were issued to Mercer as transaction costs.
The notes are convertible at the discretion of Mercer at any time prior to maturity, with a conversion price as follows:
■ Tranche 1 ($2,250,000) - any conversion within two months of the issue of the Tranche 1 Notes had a conversion price of
$0.024. After this, the conversion price was the lower of $0.02 or 92% of the lowest daily VWAP of the Company’s shares
selected by Mercer over the 10 trading days on which the Company’s shares were traded on the ASX immediately prior
to the issue of the conversion notice, subject to the Tranche 1 Conversion Price not being less than $0.018.
■ Subsequent tranches (up to $12,750,000) – the conversion price will be the lower of $0.035 or 92% of the lowest daily
VWAP of the Company’s shares selected by Mercer over the 10 trading days on which the Company’s shares are traded
on the ASX immediately prior to the issue of the conversion notice, subject to the conversion price being no less than
$0.018.
During the period, draw downs on the facility were as follows:
■ Tranche 1 (Sept 20) - $2,250,000 drawn down in exchange for convertible notes with a face value of $2,475,000.
Tranche 1 notes were fully converted during the period.
■ Tranche 2 (Nov 20) - $3,500,000 drawn down in exchange for convertible notes with a face value of $3,850,000,
maturing on 20 November 2021.
The entire hybrid contract has been designated as at fair value through profit or loss.
Financial liabilities at fair value through profit or loss
Convertible notes
Opening balance – at 1 July
Issue of convertible notes
Converted to ordinary shares
Loss on remeasurement of financial liability
Closing balance – fair value at 30 June
30-Jun-21
$
-
5,750,000
(4,810,641)
3,095,404
4,034,763
30-Jun-20
$
-
-
-
-
-
The fair value (Level 3) of the hybrid contract was determined using valuation techniques including use of a Black-Scholes
option pricing model and estimates of projected conversion prices and the following significant inputs to the valuation
at 30 June 2021:
Valuation date
Share price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Dividend yield
1. calculated using a weighted average of $0.031
TRANCHE 2
30 June 2021
$0.037
$0.018 to $0.0351
20 Nov 2021
70%
0.05%
0%
51
16. CONTRIBUTED EQUITY AND RESERVES
a) Contributed equity
Issued and paid up capital is recognised at the fair value of the consideration received by the Group. Any transaction costs
arising on the issue of ordinary shares are recognised directly in equity as a reduction of the proceeds received.
Ordinary shares on issue, fully paid
Unissued shares
Reconciliation of movement in share capital
Opening balance at 1 July 2019
Exercise of listed options – 5 Jul 2019
Issue of capital raising placement shares – 29 Aug 2019
Conversion of M3 performance rights – 9 Sep 2019
Issue of shares to vendor of Panax s.r.o – 9 Sep 2019
Issue of priority offer placement shares – 16 Sep 2019
Release of VHL Shares – 12 November 2019
Issue of Shares as consideration for services – 29 Nov 2019
Issue of capital raising placement shares – 26 Feb 2020
Issue of share purchase plan – 18 Mar 2020
Issue of capital raising placement shares – 4 May 2020
Issue of shares in lieu of cash payment – 4 May 2020
Less: share issue costs
Closing balance at 30 June 2020
Conversion of performance rights – 10 Jul 2020
Shares to consultants in lieu of cash – 12 Aug 2020
Issue via cleansing prospectus – 12 Aug 2020
Conversion of performance rights – 12 Aug 2020
Commencement shares Mercer facility1 – 15 Sept 2020
Conversion of Convertible Notes1 – 13 Nov 2020
Shares to consultants in lieu of cash – 23 Nov 2020
Acquisition of MCC2 – 23 Nov 2020
Conversion of Convertible Notes1 – 10 Dec 2020
Conversion of Convertible Notes1 – 21 Dec 2020
Placement shares on LSE listing – 10 Feb 21
Conversion of Convertible Notes1 – 4 Mar 2021
Exercise of $0.065 options – 29 Mar 21
Exercise of $0.05 options – 15 Apr 21
Acquisition of MedicaNL2 (Tranche 1) – 10 May 21
Shares to supplier in lieu of cash – 14 Jun 2021
Exercise of MXCOE options – various dates
Unissued Shares
Less: costs of issue
30-Jun-21
NUMBER
30-Jun-20
NUMBER
2,319,502,595
-
2,319,502,595
1,575,612,348
-
1,575,612,348
30-Jun-21
$
80,311,983
4,200,000
84,511,983
Issue Price
0.065
0.04
0.041
0.04
0.04
0.06974
0.034
0.032
0.027
0.027
0.027
0.031
0.022
0.020
0.034
0.024
0.021
0.022
0.022
0.030
0.024
0.0266
0.070
0.065
0.050
0.067
0.03
0.045
No. Of Shares
1,213,383,685
87,426
118,750,000
3,638,000
5,850,875
25,001,000
-
4,411,765
31,250,000
42,313,301
129,630,000
1,296,296
1,575,612,348
8,000,000
42,717,523
50,000
5,000,000
9,375,000
12,817,884
12,010,756
45,454,545
25,773,196
51,282,051
440,677,967
36,250,000
9,250,000
1,200,000
26,884,731
8,804,103
8,342,491
2,319,502,595
30-Jun-20
$
60,149,457
-
60,149,457
Amount
49,133,819
5,683
4,750,000
149,158
234,035
1,000,040
720,773
150,000
1,000,000
1,142,459
3,500,010
35,000
(1,671,520)
60,149,457
248,000
939,786
1,000
170,000
225,000
269,176
259,475
1,000,000
773,196
1,230,769
11,722,034
2,537,500
601,250
60,000
1,800,000
260,550
375,413
4,200,000
(2,310,623)
84,511,983
1. In September 2020 the Company entered into a $15,000,000 convertible note facility with Mercer Street Global Opportunity Fund,
in exchange for notes with a face value of $1.00 each, being 110% of the funding received. During the period, $225,000 in equity
was issued as transaction costs with $2,250,000 worth of notes converting into ordinary shares. Refer to note 15 for additional
information.
2. During the year, the Company acquired Medicinal Cannabis Clinics, an operating telehealth clinic for $1,400,000 including $1,000,000
by way of equity. In addition, the Company acquired a clinical research organisation MedicaNL for $6,000,000 by way of equity, with
$1,800,000 issued during the year. Refer to note 12 for additional information.
Ordinary shares participate in dividends and the proceeds on winding up of the parent entity in proportion to the number
of shares held. At a shareholders’ meetings each ordinary share is entitled to one vote when a poll is called, otherwise
each shareholder has one vote on a show of hands. Ordinary shares have no par value.
52
Capital risk management
The Group’s objective when managing capital is to safeguard their ability to continue as a going concern, so that they can
continue to provide returns to shareholders and benefits to other stakeholders and to maintain an optimal capital structure
to reduce the cost of capital.
In order to maintain or adjust the capital structure the Group may adjust the amount of dividends paid to shareholders,
return capital to shareholders, issue new shares or sell assets to reduce debt.
Consistent with others in the industry, the Group manages its capital by assessing the Group’s financial risk and adjusts
its capital structure in response to changes in these risks and in the market. These responses include the management of
debt levels, distributions to shareholders and share issues.
There have been no changes in the strategy adopted by management to control the capital of the Group since the prior
year. The Group is not subject to any externally imposed capital requirements.
b) Reserves
i. Share based payment reserve
Opening balance at 1 July
Conversion of performance rights (note 16a)
Release of VHL shares
Share based payment vesting expense (note 28)
ii. Foreign currency translation reserve
Opening balance at 1 July
Currency translation differences arising during the year
30-Jun-21
$
5,380,904
(418,000)
-
2,527,579
7,490,483
30-Jun-21
$
85,284
127,097
212,381
30-Jun-20
$
4,556,418
(149,158)
(720,773)
1,694,417
5,380,904
30-Jun-20
$
33,928
51,356
85,284
Exchange differences arising on translation of the foreign controlled entities are taken to the foreign currency translation
reserve as described above. The reserve is recognised in profit and loss when the net investment is disposed of.
17. DIVIDENDS
No dividends have been paid or provided during the year.
53
18. EARNINGS PER SHARE
Basic earnings per share
Basic earnings per share is calculated by dividing the net profit or loss after income tax attributable to equity holders of the
Company, 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 year.
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 post income tax effect of interest and other financing costs associated with dilutive potential ordinary share and the
weighted average number of shares assumed to have been issued for no consideration in relation to dilutive potential
ordinary shares.
Earning per share
Basic loss per share (cents)
Diluted loss per share (cents)
Reconciliation of earnings to profit or loss
(Loss) used in calculating basic and diluted EPS
Earnings per share for continuing operations
Basic loss per share (cents)
Diluted loss per share (cents)
Reconciliation of earnings to profit or loss
(Loss) used in calculating basic and diluted EPS
Weighted average number of ordinary shares and potential ordinary shares
Weighted average number of ordinary shares used in calculating basic and diluted EPS
30-Jun-21
30-Jun-20
(0.83)
(0.83)
(1.40)
(1.40)
$
(15,869,978)
$
(19,363,089)
(0.81)
(0.81)
(1.36)
(1.36)
$
(15,407,341)
$
(18,762,662)
Number
Number
1,906,114,879
1,382,194,646
At 30 June 2021, the Company had on issue 37,550,000 performance rights (2020: 20,000,000), 163,062,069 options
(2020: 184,334,538) and 3,850,000 convertible notes (2020: nil). Given the Group made a loss during the current financial
year, these potential shares are considered non-dilutive and therefore not included in the diluted EPS calculation.
19. FINANCIAL RISK MANAGEMENT
The Group’s financial instruments consist mainly of cash at bank, payables, receivables and the convertible notes.
The Group has not formulated any specific management objectives and policies in respect to debt financing, derivatives
or hedging activity. As a result, the Group has not formulated any specific management objectives and policies in respect
to these types of financial instruments. Should the Group change its position in the future, a considered summary of these
policies will be disclosed at that time.
The Group’s current exposure to the risk of changes in the market is managed by the Board of Directors.
Market risks
The Group is exposed to a variety of financial risks through its financial instruments for example, interest rate risk, liquidity
risk and credit risk, equity price risk on the convertible notes, as well as foreign currency risk.
54
Interest rate risk
At reporting date, other than leases and the convertible notes carried at fair value, the Group does not have long term
borrowings and its exposure to interest rate risk is assessed as low. The group monitors its interest rate risk through
sensitivity analysis, as outlined below.
The consolidated group’s exposure to interest rate risk which is the risk that a financial instrument’s value will fluctuate as
a result of changes in market interest rates and the effective weighted average interest rates on classes of financial assets
of the Group are summarised in the following tables:
30 June 2021
Financial assets
Cash and cash equivalents
Trade and other receivables
Financial liabilities
Trade and other payables
Convertible note
Lease liabilities
30 June 2020
Financial assets
Cash and cash equivalents
Trade and other receivables
Financial liabilities
Trade and other payables
Lease liabilities
Floating interest
rate
$
1 Year or less
$
Over 1 to 5
years
$
Non-interest
bearing
$
Remaining
contractual
maturities
$
Weighted
average
interest rate
%
5,433,241
-
5,433,241
5,433,241
-
5,433,241
-
-
-
-
1,507,675
1,507,675
5,433,241
1,507,675
6,940,916
0.14%
-
-
1,982,807
1,982,807
1,873,373
-
1,873,373
-
1,899,224
1,899,224
-
-
209,433
209,433
-
-
1,773,373
1,773,373
1,796,235
4,034,763
-
5,830,998
1,873,373
-
1,873,373
-
-
-
-
468,506
468,506
-
53,924
53,924
-
1,845,300
1,845,300
2,705,818
-
2,705,818
1,796,235
4,034,763
1,982,807
7,813,805
1,873,373
468,506
2,341,879
2,705,818
1,899,224
4,605,042
0.65%
1. The initial investment amount for the convertible notes represented a 10% discount to their face value. As the notes are accounted
for at fair value through profit or loss, the Group would have exposure to fair value movements arising from changes in market
interest rates.
At 30 June 2021, a reasonably possible change in interest rates would not have resulted in a material change to the
Group’s post-tax loss or net assets for the year.
Liquidity risk
Liquidity risk is the risk that the Group will not be able to meet its financial obligations as they fall due. The Group’s
approach to managing liquidity is to ensure, as far as possible, that it will always have sufficient cash to meet its liabilities
when due, under both normal and stressed conditions, without incurring unacceptable losses or risking damage to the
Group’s reputation. The Group monitors forecast cash flows on regular basis to manage its liquidity risk.
Credit risk
Management has assessed the credit risk exposure as minimal at reporting date. Credit risk arises from exposure to trade
receivables, deposits with banks and other receivables, the balances of which at 30 June 2021 represent the Group’s
maximum exposure to credit risk. Management monitors its exposure to ensure recovery and repayment of outstanding
amounts. Cash deposits are only made with reputable banking institutions.
Foreign currency risk
The Group operates internationally and is exposed to foreign exchange risk arising from various currency exposures,
primarily with respect to the GBP (£), Euro (€), ILS (₪) and CZK (Kč).
Foreign exchange risk arises from future commercial transactions and recognised assets and liabilities denominated in a
currency that is not the entity’s functional currency. The risk is measured using cash flow forecasting.
The consolidated entity has not entered into any derivative financial instruments to hedge such transactions and
anticipated future receipts or payments that are denominated in a foreign currency. The board manages the purchase of
foreign currency to meet operational requirements.
55
The consolidated entity’s exposure to foreign currency risk at the reporting date was not material. A reasonably possible
change in the value of the Australian dollar against the above currencies at 30 June would not have had a material effect
on the Group’s post-tax loss or net assets.
20. FAIR VALUE MEASUREMENT OF FINANCIAL INSTRUMENTS
All assets and liabilities for which fair value is measured or disclosed in the financial statements are categorised within the
fair value hierarchy, described as follows, based on the lowest level input that is significant to the fair value measurement
as a whole:
■ Level 1 — Quoted (unadjusted) market prices in active markets for identical assets or liabilities
■ Level 2 — Valuation techniques for which the lowest level input that is significant to the fair value measurement is
directly or indirectly observable
■ Level 3 — Valuation techniques for which the lowest level input that is significant to the fair value measurement is
unobservable
For assets and liabilities that are recognised in the financial statements on a recurring basis, the Group determines
whether transfers have occurred between Levels in the hierarchy by re-assessing categorisation (based on the lowest
level input that is significant to the fair value measurement as a whole) at the end of each reporting period.
The following table presents the Group’s financial assets and liabilities measured and recognised at fair value.
30 June 2021
Financial assets
Other financial assets (equity investments)
Closing balance at 30 June 2021
Financial liabilities
Other financial liabilities (convertible note)
Closing balance at 30 June 2021
30 June 2020
Financial assets
Other financial assets (equity investments)
Closing balance at 30 June 2020
Level 1
$
Level 2
$
Level 3
$
564,186
564,186
4,034,763
4,034,763
Level 3
$
Total
$
564,186
564,186
4,034,763
4,034,763
Total
$
-
-
-
-
Level 2
$
-
-
559,597
559,597
673,740
673,740
-
-
-
-
Level 1
$
114,143
114,143
Refer to note 10 for disclosures in relation to the loan accounted for as fair value through profit or loss (level 3).
a) Valuation techniques used to derive Level 1 fair values
The fair value of financial instruments recognised under Level 1 are measured based on the active market value,
determined in this case by the value a third party is willing to pay for the assets.
b) Valuation techniques used to derive Level 3 fair values
The fair value of financial instruments that are not traded in an active market are determined using valuation techniques.
These valuation techniques maximise the use of observable market data where it is available and rely as little as possible
on entity specific estimates.
If one or more of the significant inputs is not based on observable market data, the instrument is included in level 3.
A significant unobservable input to the valuation of the Group’s investment in an unlisted entity classified within level 3 of
the fair value hierarchy was information obtained from the investee in relation to the value per share of the most recent
capital raising announced by the entity, which was CAD 0.21/share ($0.22/share). A 10% increase or decrease in the value
per share of the unlisted entity would have a corresponding fair value movement on the carrying value of the Group’s
investment.
Refer to note 15 for additional disclosures on the other financial liability accounted for at fair value through profit or loss.
c) Fair value of other financial instruments
The Group also has a number of financial instruments that are not measured at fair value in the balance sheet.
The carrying value of cash, trade receivables and payables is a reasonable approximation of their fair values due to their
short-term nature.
56
21. CONTROLLED ENTITIES
The consolidated financial statements of the Group include:
Parent Entity:
MGC Pharmaceuticals Ltd
Subsidiaries of MGC Pharmaceuticals Ltd:
MGC Pharma (UK) Limited
MGC Research (Aus) Pty Ltd
Medicinal Cannabis Clinics Pty Ltd
Subsidiaries of MGC Pharma (UK) Limited:
MGC Pharmaceuticals d.o.o
Panax Pharma s.r.o
MGC Nutraceuticals d.o.o1
MGC Pharma (Malta) Holdings Limited
MGC Pharma (Malta) R&D Limited
MedicaNL Israel 2019 Ltd
Subsidiaries of MGC Pharma (Malta) Holdings Limited
MGC Pharma (Malta) Property Limited
MGC Pharma (Malta) Operations Limited
* Percentage of voting power in proportion to ownership
1. Refer note 4 for further details
Country of
incorporation
Australia
UK
Australia
Australia
Slovenia
Czech Republic
Slovenia
Malta
Malta
Israel
Malta
Malta
Percentage Owned (%)*
30-Jun-21
30-Jun-20
100
100
100
100
87
100
100
100
100
100
100
100
100
-
100
87
100
100
100
-
100
100
22. SEGMENT REPORTING
The Group identifies operating segments on the basis of internal reports about components of the Group that are
regularly reviewed by the chief operating decision maker (“CODM”) in order to allocate resources to the segments and to
assess their performance.
The Group has assessed its operating segments and determined that the Group’s operations comprise one segment,
being production and supply of medicinal cannabis products, on the basis that the Group’s CODM reviews financial
information in relation to operating results at the whole of Group level.
Geographic information on the Group’s revenue by location of operations for the period and non-current assets
at 30 June 2021 is as follows:
30 June 2021
Sales revenue
Total non-current assets
30 June 2020
Sales revenue
Total non-current assets
Malta
$
-
6,363,232
Israel
$
255,102
5,654,899
Slovenia
$
1,091,5781
847,169
Australia
$
1,653,4671
1,400,000
-
2,957,260
-
-
1,938,4281
1,009,824
140,741
-
1. Three external customers individually contributed greater than 10 per cent of Group revenue, being $1,140,513, $686,866
and $487,301 respectively (30 June 2020 two customers comprising: $1,056,390 and $573,772 respectively).
57
23. CONTINGENCIES AND COMMITMENTS
a) Commitments
No later than one year
Later than one year and not later than five years
Total commitments
30-Jun-21
$
175,000
1,036,446
1,211,446
30-Jun-20
$
779,070
536,023
1,315,093
Commitment relate to Research and Development Agreements held with Royal Melbourne Institute of Technology, for
both the Breeding and Pre-clinical Research and the Library of Cannabinoids Project, in addition to the University of Notre
Dame CogniCann® Clinical Trial.
Malta long-term leases – construction commitments
Larger site - 65 year lease
Further to the approval of the Company’s original planned project in Malta, the Company agreed to invest a minimum of
€6,000,000 in improvements to site, plant, machinery and equipment within 3 years from the date of allocation of the site.
On allocation of a site, the Company also entered into a long-term lease with Malta Industrial Parks (refer note 14 for
further details). The Emphyteutical lease requires that the allocated site is used solely for industrial purposes and that
the erection of proper, solid buildings costing no less than €2,700,000, net of value added tax, was to commence within
three months of the date of the necessary approvals being received, being 8 August 2019, but be completed no later than
eighteen months from the date all permits by law are issued. It is the intention of management that construction will not
commence until the current construction site is completed and GMP certified, which is anticipated in mid-late 2022.
Smaller site – 5 year lease – Artemic facility
A second lease has been signed with Malta Enterprise, which includes a commitment to invest €3,841,200 by way of
improvements on the premises within three years. The Group has received a grant to cover 80% of these costs up to
€3,073,000 (~$4,925,000) (refer to Note 13c) and construction on the facility to produce Artemic is underway with a
construction contract signed with BioPharmax with completion expected in October 2021. As at 30 June 2021 an amount
of €1,514,463 ($2,442,682) had been incurred towards this commitment.
Employment Agreement Commitments
On 1 January 2021, the Company engaged a Chief Sales Officer, with a large part of the salary package made up of
performance equity. 7,692,308 options were issued during the year as part of this agreement as outlined in note 28, with
the performance conditions for the following two tranches not yet determined at balance date. The agreement stipulates
the following outstanding commitments as at 30 June 2021;
■ 7,692,307 issued within 15 months from the Commencement Date at an exercise price of $0.026 expiring on
31 March 2024 and vesting on the latest to occur of (i) the second anniversary of the Effective Date, or (ii)
achievement of a key performance indicator to be further agreed upon by the Parties prior to or on the first
anniversary of the commencement date.
■ 7,692,307 issued within 27 months from the Commencement Date at an exercise price of $0.026 expiring on
31 March 2025 and vesting on the latest to occur of (i) the second anniversary of the Effective Date, or (ii)
achievement of a key performance indicator to be further agreed upon by the Parties prior to or on the first
anniversary of the commencement date.
58
24. CASH FLOW INFORMATION
Reconciliation of Cash Flow from Operations with Loss after Income Tax
(Loss) after income tax
Cash flows excluded from loss attributable to operating activities
Non-cash flows in loss
Depreciation and amortisation
Loss on financial asset at fair value
Share based payment expense
Shares issued to extinguish financial liabilities
Loss on financial liabilities at fair value
Exchange differences
Changes in assets and liabilities, net of the effects of purchase of subsidiaries
Decrease / (increase) in inventory
Decrease / (increase) in trade and other receivables
Increase / (decrease) in trade payables and accruals
Cash flow from operations
25. AUDITOR’S REMUNERATION
Fees to Ernst & Young (Australia):
Fees for auditing the statutory financial report of the parent covering the group and auditing the
statutory financial reports of any controlled entities
Fees for other services
– R&D rebate application
Total fees to Ernst & Young (Australia)
Fees to PKF (Australia):
Fees for auditing the statutory financial report of the parent covering the group and auditing the
statutory financial reports of any controlled entities
Fees for other services
– Tax compliance
– Others
Total fees to PKF (Australia)
Fees to other overseas member firms of PKF (Australia):
Fees for auditing the financial report of any controlled entities
Total fees to overseas member firms of PKF (Australia)
Total auditor’s remuneration
30-Jun-21
$
30-Jun-20
$
(15,871,978)
(19,370,226)
491,408
546,995
1,647,715
1,456,698
3,157,597
92,442
481,130
5,117,767
854,916
-
2,098,064
(82,205)
(470,207)
(2,220,312)
(819,970)
(11,989,612)
(263,437)
271,912
935,212
(9,956,867)
30-Jun-21
$
30-Jun-20
$
176,333
163,350
40,580
216,913
-
163,350
-
-
-
-
-
-
216,913
8,548
-
1,900
10,448
1,771
1,771
175,569
59
26. PARENT COMPANY DISCLOSURES
The financial information for the parent entity, MGC Pharmaceuticals Ltd, has been prepared on the same basis as the
consolidated financial statements.
i) Summary of financial information
The individual financial statements for the parent entity show the following aggregate amounts:
Current assets
Non-current assets
Total Assets
Current liabilities
Total Liabilities
Contributed equity
Share based payment reserve
Accumulated losses
Total Equity
Loss for the year
Total comprehensive loss for the year
30-Jun-21
$
3,404,114
14,697,179
18,101,293
30-Jun-20
$
1,723,652
2,400,695
4,124,347
4,275,394
4,275,394
1,029,991
1,029,991
80,311,983
7,490,483
(73,976,567)
13,825,899
60,149,458
4,080,904
(61,136,006)
3,094,356
(11,540,561)
(11,540,561)
(19,543,940)
(19,543,940)
ii) Commitments and contingent liabilities of the parent
The parent entity did not have any contingent liabilities or commitments as at 30 June 2021 (30 June 2020: nil) other than
as disclosed at note 23.
iii) Guarantees entered into the parent entity
There were no guarantees entered into by the parent entity.
27. RELATED PARTY TRANSACTIONS
a) Key Management Personnel Remuneration
Compensation
The aggregate compensation made to directors and other members of key management personnel of the consolidated
entity is set out below:
30-Jun-21
$
861,968
-
-
432,000
1,293,968
30-Jun-20
$
1,045,711
-
-
124,391
1,170,102
Short-term employee benefits
Post-employment benefits
Long-term benefits
Share-based payments
60
b) Transactions with Director related entities
Directors and officers, or their personally related entities, hold positions in other entities that result in them having controls
or significant influence over the financial or operating policies of those entities.
Details of non-remuneration related transactions including amounts receivable and payable at the end of the year are as
follows:
Transactions
Full Year
30-Jun-21
Full Year
30-Jun-20
Balances
(owing to)/ owed by
Full Year
30-Jun-21
Full Year
30-Jun-20
Related Party
CHIEFTAIN SECURITIES
PTY LTD (CHIEFTAIN)
CHIEFTAIN SECURITIES
PTY LTD (CHIEFTAIN)
CHIEFTAIN SECURITIES (WA)
PTY LTD (CHIEFTAIN WA)
GRAFT POLYMER (UK) LIMITED
AUSTRALIA CANNABIS
VENTURES LIMITED (ACV)
Relationship Nature of transactions
$
$
$
$
(i)
(i)
(ii)
(iii)
(iv)
Corporate services from Chieftain –
1 Jul 20 to 31 Dec 20
Charges from Chieftain for capital
raising costs
Corporate services from Chieftain –
1 Jan 21 to 30 June 21
Services charges from/ (recharges
to) GPO for development for MGC
Proprietary drug delivery technology
(Re-charges) to ACV for corporate
administrative costs
30,000
60,000
-
116,594
30,000
-
-
-
-
(5,500)
-
-
409,446
510,859
(6,820)
(40,000)
(10,000)
-
-
-
(i) Mr Brett Mitchell is a Director and holds a 25% shareholding in Chieftain Securities Pty Ltd.
(ii) Mr Brett Mitchell is a Director and holds a 25% shareholding in Chieftain Securities (WA) Pty Ltd.
(iii) Mr Roby Zomer is Executive Chairman and shareholder of Graft Polymer (UK) Limited, who is developing the
proprietary nano-emulsion and nano-particle drug delivery platform for MGC Pharma medicines.
(iv) Mr Brett Mitchell is an Executive Chairman and shareholder of Australian Cannabis Ventures Limited
c) Other related party transactions
There were no other related party transactions.
28. SHARE BASED PAYMENTS
Share based compensation relating to share options are recognised at fair value.
The fair value of the options is recognised as an employee benefit expense in the statement of profit or loss and other
comprehensive income, with a corresponding increase in equity. The total amount to be expensed is determined by
reference to the fair value of the options granted, which includes any market performance conditions and the impact of
any non-vesting conditions but excludes the impact of any service and non-market performance vesting conditions.
The total expense is recognised over the vesting period, which is the period over which all of the specified vesting
conditions are to be satisfied.
Upon exercise of share options, the proceeds received net of any directly attributable transaction costs are allocated to
share capital.
The fair value for all share options, as detailed below, are determined using a binomial option pricing method that takes
into account the exercise price, the term of the option, the probability of exercise, the share price at grant date and
expected volatility of the underlying share, the expected dividend yield and the risk-free interest rate for the term of the
option.
The inputs used for the valuations are tabled below for each class of security issued.
The expected life of the options is based on historical data and is not necessarily indicative of exercise patterns that may
occur. The expected volatility reflects the assumption that the historical volatility is indicative of future trends, which may
also not necessarily be the actual outcome. The probability of the performance conditions occurring, where applicable are
included in determining the fair value of the options.
61
The assessed fair value at grant date of share based payments granted during the period was determined using a
binomial option pricing model that takes into account the exercise price, the price of the underlying share at grant date, the
life of the option, the volatility of the underlying share, the risk-free rate and expected dividend payout and any applicable
vesting conditions.
Management was required to make assumptions and estimates in order to determine the inputs into the binomial option
pricing model.
a) Performance Rights
2021
Directors
On 31 March 2021, the Company agreed to issue performance rights to the Directors and other management personnel,
to incentivise and retain its workforce. The performance rights issued to Directors were subject to shareholder approval,
which was received subsequent to year-end on 12 August 2021:
# VESTING MILESTONE
A If and once the share price of MGC Pharma, at any time prior to or on 1 April 2022,
PERFORMANCE RIGHTS MILESTONE DATE
has a 10- trading day VWAP equal to or exceeding $0.0875 and the
participant remaining a director as at 1 April 2022
B If and once the share price of MGC Pharma, at any time prior to or on 1 April 2023,
has a 10- trading day VWAP equal to or exceeding $0.105 and the
participant remaining a director as at 1 April 2022
C 18 months continued service up to 30 June 2021 or if employment commenced
after 1 January 2020, continued employment from the commencement date until
30 June 2021
17,100,000
1 Apr 22
39,900,000
1 Apr 23
7,200,000
27,550,000
30 Jun 21
The performance conditions were chosen to best align with the Company’s strategic goals and objectives to enhance
shareholder value. There was no performance condition associated with Milestone C. The grant of the performance
rights, including those without performance conditions, is considered by the Company to be a reasonable and appropriate
method to provide cost effective remuneration as the non-cash form of this benefit will allow the Company to spend a
greater proportion of its cash reserves on its operations than it would if alternative cash forms of remuneration were given
to the Related Parties.
The fair value of the performance rights for milestone C was estimated to be $0.041/right at 30 June 2021. A Monte Carlo
valuation was applied to milestones A and B to estimate the fair values at 30 June 2021, with the following inputs and
assumptions:
Valuation date
Share price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Vesting hurdle
Dividend yield
Value per right
MILESTONE A
12 Aug 21
$0.041
Nil
1 Apr 22
66%
0.0355%
$0.0875
nil
$0.038
MILESTONE B
12 Aug 21
$0.041
Nil
1 Apr 23
70%
0.0388%
$0.105
nil
$0.009
Although grant date has occurred subsequent to year-end, there was an agreement in place during the year to issue the
performance rights, and therefore they have been expensed over the relevant service periods based on an estimated
valuation at 30 June 2021, which was consistent to the valuation subsequently determined at the grant date of 12 August
2021. The milestone C performance rights fully vested during the period, while the milestone A and B rights remained
unvested and are being expensed over the service period to 1 April 2022.
62
Employees
On 23 April 2021, the Company agreed to issue its employees with performance rights to assist with both retention and
incentivisation. The terms of the performance rights are summarised below:
# VESTING MILESTONE
A If and once the share price of MGC Pharma, at any time prior to or on 1 April
2022, has a 10- trading day VWAP equal to or exceeding $0.0875 and the
participant remaining an eligible participant as at 1 April 2022
B If and once the share price of MGC Pharma, at any time prior to or on 1 April
2023, has a 10- trading day VWAP equal to or exceeding $0.105 and the
participant remaining an eligible participant as at 1 April 2022
C 18 months continued service up to 30 June 2021 or if employment commenced
after 1 January 2020, continued employment from the commencement date until
30 June 2021
PERFORMANCE RIGHTS MILESTONE DATE
3,725,000
1 Apr 22
9,275,000
1 Apr 23
14,550,000
27,550,000
30 Jun 21
The performance conditions were chosen to best align with the Company’s strategic goals and objectives to enhance
shareholder value. There was no performance condition associated with Milestone C. The grant of the performance
rights, including those without performance conditions, is considered by the Company to be a reasonable and appropriate
method to provide cost effective remuneration as the non-cash form of this benefit will allow the Company to spend a
greater proportion of its cash reserves on its operations than it would if alternative cash forms of remuneration were given
to the employees.
The fair value of the performance rights for milestones C was determined to be $0.061/right, based on the Company’s
share price on the grant date. A Monte Carlo valuation was applied to milestones A and B, with the following inputs and
assumptions:
Valuation date
Share price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Vesting hurdle
Dividend yield
Value per right
MILESTONE A
23 Apr 21
$0.061
Nil
1 Apr 22
100%
0.0355%
$0.0875
nil
$0.0301
MILESTONE B
23 Apr 21
$0.061
Nil
1 Apr 23
100%
0.0388%
$0.105
nil
$0.0365
In addition, a total of 500,000 performance rights have been agreed to be issued to the Australian key account manager,
with service conditions over a one- and two-year period. These have not been issued as yet, however have been valued
and expensed over the contract execution date of 30 April 2021, and valued as at the share price on that day being
$0.06 per right.
Reconciliation of Performance Rights
OPENING
BALANCE
28,000,000
-
2021
2020
GRANTED AS
COMPENSATIONi
EXERCISED
LAPSED
OUTSTANDING AT
30 JUNE
OUTSTANDING AND
EXERCISABLE AT
30 JUNE
27,550,000
28,000,000
(13,000,000)
-
(5,000,000)
-
37,550,000
28,000,000
14,550,000
13,000,000
i. Refer to “Performance rights” section above for details of rights granted and vested during the period, which Director rights were still
subject to shareholder approval at 30 June 2021 and therefore had not yet been issued.
63
2020
Directors
During the prior year, the Company issued performance rights to two Directors following approval at its AGM
on 29 November 2019, with the following key terms and conditions:
# VESTING MILESTONE
1. GMP approval for Malta facility
2. Holding of Director position on the Board of the Company by 31 December
PERFORMANCE RIGHTS MILESTONE DATE
5,000,000
31 Dec 21
2019
5,000,000
31 Dec 19
3. Holding of Director position on the Board of the Company by 31 December
2020 and achieving share value of minimum 8c for a minimum 10
consecutive days
4. Holding of Director position on the Board of the Company by 31 December
2021 and achieving share value of minimum 10c for a minimum 10
consecutive days
5,000,000
31 Dec 20
5,000,000
20,000,000
31 Dec 21
The fair value of the performance rights for milestones 1 and 2 was determined to be $0.034/right, based on the
Company’s share price on the grant date. A Monte Carlo valuation was applied to milestones 3 and 4, with the following
inputs and assumptions:
Valuation date
Share price
Exercise price
Vesting date
Expiry date
Expected future volatility
Risk free rate
Vesting hurdle
Dividend yield
Value per right
Employees
MILESTONE 3
29 Nov 19
$0.0340
Nil
N/A
31 Dec 20
70%
0.68%
$0.08
nil
$0.00848
MILESTONE 4
29 Nov 19
$0.0340
Nil
N/A
31 Dec 21
70%
0.68%
$0.10
nil
$0.01213
The Group also issued 8m performance rights to certain key employees following shareholder approval on 29 November
2019, with both of the following key conditions to be met (upon conversion, these shares are restricted until 30 June 2020):
#
1.
2.
CONDITIONS
Continuous service of the holder in their capacity as an eligible participant, or in a role otherwise agreed by the Board by 31
January 2020
The Company achieves more than 2,000 prescribed products of its phytocannabinoid-derived medicines
The fair value of the performance rights was determined to be $0.031/right based on the Company’s share price on the
grant date. These rights vested on 31 January 2020.
b) Options
2021
As part of the LSE Listing and IPO in February 2021, the Company agreed to issue to its broker 26,440,678 options subject
to shareholder approval, which was subsequently received on 31 March 2021.
In addition, on 1 January 2021 the Company agreed to issue 7,692,308 performance options to its chief sales officer.
These options shall vest upon the later of 12months continued service or the company achieving global sales in excess of
$1million in consecutive months. A 100% probability has been assigned to these options for valuation purposes.
64
Inputs to the valuation of the abovementioned options are identified in the table below.
Number options issued
Grant date
Spot price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Dividend yield
Value per option
BROKER OPTIONS
26,440,678
31 Mar 21
$0.062
£0.01475
31 Mar 23
85%
0.09%
nil
$0.042
EMPLOYEE OPTIONS
7,692,308
01 Jan 21
$0.025
$0.026
31 Mar 23
85%
0.08%
nil
$0.012
The broker options have been valued based on the fair value of the equity instruments issued, as the Company was unable
to reliably determine the fair value of the services provided.
Table of share-based payment options
DESCRIPTION
Unlisted options exercisable at £0.01475 expiring 31 Mar 2023
Unlisted options exercisable at $0.026 expiring 31 Mar 2023
Unlisted options exercisable at $0.05 expiring 31 Aug 2023
Unlisted options exercisable at $0.06 expiring 31 Aug 2023
Unlisted options exercisable at $0.07 expiring 31 Aug 2023
Unlisted options exercisable at $0.065 expiring 31 Mar 2021
TOTAL
LAPSED
OPENING
BALANCE GRANTED EXERCISED
-
-
(1,200,000)
-
-
(9,250,000)
-
- 26,440,678
-
7,692,308
-
-
-
17,500,000
-
-
17,500,000
-
-
17,500,000
16,000,000
(6,750,000)
-
68,500,000 34,132,986 (10,450,000) (6,750,000)
OUTSTANDING
AND
EXERCISABLE
AT 30 JUNE 2021
26,440,678
7,692,3081
16,300,000
17,500,000
17,500,000
-
85,432,986
1. Refer to note 23 for additional options have been agreed and not yet issued
2020
Equity Capital Markets Advisor
Pursuant to agreement with the Group’s Equity Capital Markets Advisor, the Company agreed to issue 43.5m options over
3 tranches, with the first two tranches issued on 16 September 2019, and the final tranche following shareholder approval.
The following table highlights the terms, conditions and inputs used for the valuation of the options using the Hoadley
EOS2 valuation model; a valuation model was applied as the Company were unable to define a suitable fair value on the
services being provided:
Number options issued
Issue date
Valuation date
Spot price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Dividend yield
Value per option
TRANCHE 1
14,500,000
16 Sept 19
16 Sept 19
$0.040
$0.05
31 Aug 23
85%
0.91%
nil
$0.00182
TRANCHE 2
14,500,000
16 Sept 19
16 Sept 19
$0.040
$0.06
31 Aug 23
85%
0.91%
nil
$0.0173
TRANCHE 3
14,500,000
23 Dec 19
18 Oct 19
$0.035
$0.07
31 Aug 23
85%
0.75%
Nil
$0.0135
65
Joint Leading Managers
Pursuant to agreement with two of the Group’s leading managers, the Company agreed to issue 9m options over
3 tranches, issued following shareholder approval at the AGM on 29 November 2019.
The following table highlights the terms, conditions and inputs used for the valuation of the options using the Hoadley
EOS2 valuation model; a valuation model was applied as the Company were unable to define a suitable fair value on the
services being provided:
Number options issued
Issue date
Valuation date
Spot price
Exercise price
Expiry date
Expected future volatility
Risk free rate
Dividend yield
Value per option
TRANCHE 1
3,000,000
23 Dec 19
18 Oct 19
$0.035
$0.05
31 Aug 23
85%
0.91%
nil
$0.0152
TRANCHE 2
3,000,000
23 Dec 19
18 Oct 19
$0.035
$0.06
31 Aug 23
85%
0.91%
nil
$0.0143
TRANCHE 3
3,000,000
23 Dec 19
18 Oct 19
$0.035
$0.07
31 Aug 23
85%
0.75%
Nil
$0.0135
Share-based payment expense
For the year ended 30 June 2021, the Group has recognised $1,419,602 of share-based payment expenses in the
statement of profit or loss (30 June 2020: $854,915) relating to share-based payments to directors and employees.
The Group has also recognised $1,101,977 (30 June 2020: 839,500) of share-based payment expense in relation to capital
raising costs (refer to note 16).
29. EVENTS AFTER THE REPORTING DATE
On 8 July 2021 Mercer elected to convert $500,000 of its convertible notes into 14,792,899 ordinary shares, with
an additional conversion on 3 September 2021 of $1,250,000 into 35,714,286 ordinary shares, leaving a balance of
$2,100,000 (face value) in convertible notes at the date of this report.
On 12 August 2021 the Company held a General Meeting with performance rights issued to the Directors. As these
performance rights were agreed to be issued during the financial year, then have been expensed over the relevant service
conditions within the current year.
On 26 August, the Company executed a US$24 million supply agreement with AMC Holdings Inc of MGC phytomedicine
products over three years, with a minimum of US$3 million within the first year.
66
12
DIRECTORS’
DECLARATION
Directors’ Declaration
The Directors’ of the Company declare that in their opinion:
1. The financial statements and notes, as set out in pages 30 to 66, are in accordance with the Corporations Act 2001
and:
a) comply with Accounting Standards and the Corporations Regulations 2001;
b) are in accordance with International Financial Reporting Standards, as stated in note 2a to the financial statements;
c) give a true and fair view of the consolidated group’s financial position as at 30 June 2021 and its performance for
the year ended on that date; and
d) representations made throughout the Directors report are fair and reasonable.
2. The Directors have been given the declaration required by section 295A of the Corporations Act 2001.
3. The remuneration disclosures contained in the Remuneration Report comply with s300A of the Corporations Act 2001.
4. In the Directors opinion, subject to the matters set out in note 2(b) to the financial statements, there are reasonable
grounds to believe that the Company will be able to pay its debts as and when they become due and payable.
This declaration is made in accordance with a resolution of the Board of Directors.
Roby Zomer
Managing Director
30 September 2021
67
13
INDEPENDENT AUDITOR’S
REPORT TO MEMBERS
Independent Auditor’s Report to Members
Ernst & Young
11 Mounts Bay Road
Perth WA 6000 Australia
GPO Box M939 Perth WA 6843
Tel: +61 8 9429 2222
Fax: +61 8 9429 2436
ey.com/au
Independent auditor's report to the members of MGC Pharmaceuticals
Limited
Report on the audit of the financial report
Opinion
We have audited the financial report of MGC Pharmaceuticals Limited (the Company) and its
subsidiaries (collectively the Group), which comprises the consolidated statement of financial position
as at 30 June 2021, the consolidated statement of profit or loss and other comprehensive income,
consolidated statement of changes in equity and consolidated statement of cash flows for the year
then ended, notes to the financial statements, including a summary of significant accounting policies,
and the directors declaration.
In our opinion, the accompanying financial report of the Group is in accordance with the Corporations
Act 2001, including:
a)
giving a true and fair view of the consolidated financial position of the Group as at 30 June
2021 and of its consolidated financial performance for the year ended on that date; and
b)
complying with Australian Accounting Standards and the Corporations Regulations 2001.
Basis for opinion
We conducted our audit in accordance with Australian Auditing Standards. Our responsibilities under
those standards are further described in the Auditor’s Responsibilities for the Audit of the Financial
Report section of our report. We are independent of the Group in accordance with the auditor
independence requirements of the Corporations Act 2001 and the ethical requirements of the
Accounting Professional and Ethical Standards Board’s APES 110 Code of Ethics for Professional
Accountants (including Independence Standards) (the Code) that are relevant to our audit of the
financial report in Australia. We have also fulfilled our other ethical responsibilities in accordance with
the Code.
We believe that the audit evidence we have obtained is sufficient and appropriate to provide a basis
for our opinion.
Material uncertainty related to going concern
We draw attention to Note 2(a) of the financial report, which describes the principal conditions that
raise doubt about the Group’s ability to continue as a going concern. These events or conditions
indicate that a material uncertainty exists that may cast significant doubt on the Group’s ability to
continue as a going concern. Our opinion is not modified in respect of this matter.
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68
Key audit matters
Key audit matters are those matters that, in our professional judgment, were of most significance in
our audit of the financial report of the current year. In addition to the matter described in the Material
uncertainty related to going concern section of our report, we have determined the matters described
below to be the key audit matters to be communicated in our report. These matters were addressed in
the context of our audit of the financial report as a whole, and in forming our opinion thereon, but we
do not provide a separate opinion on these matters. For each matter below, our description of how
our audit addressed the matter is provided in that context.
We have fulfilled the responsibilities described in the Auditor’s Responsibilities for the Audit of the
Financial Report section of our report, including in relation to these matters. Accordingly, our audit
included the performance of procedures designed to respond to our assessment of the risks of
material misstatement of the financial report. The results of our audit procedures, including the
procedures performed to address the matters below, provide the basis for our audit opinion on the
accompanying financial report.
1.
Impairment assessment for non-current assets
Why significant
How our audit addressed the key audit matter
The quantum of the Group’s non-current assets
is material to the Group’s financial statements
and the assessment of whether impairment
existed at 30 June 2021 in relation to these
assets required significant management
judgement.
Malta
As disclosed in Notes 11 and 14 to the financial
statements, the Group’s non-current assets in
Malta included a balance of $1.10 million for con-
struction in progress and $1.73 million for the
right-of-use asset associated with the 65-year
lease of land on which the Group intends to con-
struct its larger production facility.
As disclosed in Notes 14 and 23, the Group has
not been able to comply with all conditions under
the long-term lease agreement, including the
requirement to commence construction of the
facility within three months of the lease
agreement being signed. At 30 June 2021 and
to the date of this report, no breach notice had
been received from the lessor in this regard.
Our audit procedures included the following:
► We obtained and reviewed the Group’s
assessment of impairment triggers for its non-
current assets
► We obtained the Group’s assessment of
impairment in relation to the construction in
progress and right-of-use asset associated with
the 65-year lease in Malta at 30 June 2021
conducted on a value-in-use basis, and
performed sensitivity analysis over the key
inputs to the model, including cash flows and
discount rates
► We considered the Group’s assessment of
impairment in relation to the provisional
unallocated goodwill at 30 June 2021
► As a consequence of the global COVID-19
pandemic, the Group was unable to meet the
conditions set out in the Malta long-term lease
agreement. Through enquiry and review of the
Group’s correspondence with the lessor, we
determined that the lease agreement remains
active and that no penalties or termination
notices have been imposed by the lessor
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► We considered the adequacy of the financial
report disclosures.
The Group assessed the construction in progress
and right-of-use assets associated with the 65-
year lease for impairment at 30 June 2021 and
concluded that they were not impaired.
Goodwill
As disclosed in Note 12 to the financial
statements, the two business combinations
undertaken by the Group in the current period
resulted in total provisional unallocated goodwill
recognised of $7.05 million at 30 June 2021.
The Group assessed the provisional goodwill for
impairment and concluded that there was no
indication that it was impaired.
Information other than the financial report and auditor’s report thereon
The directors are responsible for the other information. The other information comprises the
information included in the Company’s 2021 Annual Report, but does not include the financial report
and our auditor’s report thereon.
Our opinion on the financial report does not cover the other information and accordingly we do not
express any form of assurance conclusion thereon, with the exception of the Remuneration Report
and our related assurance opinion.
In connection with our audit of the financial report, our responsibility is to read the other information
and, in doing so, consider whether the other information is materially inconsistent with the financial
report or our knowledge obtained in the audit or otherwise appears to be materially misstated.
If, based on the work we have performed, we conclude that there is a material misstatement of this
other information, we are required to report that fact. We have nothing to report in this regard.
Responsibilities of the directors for the financial report
The directors of the Company are responsible for the preparation of the financial report that gives a
true and fair view in accordance with Australian Accounting Standards and the Corporations Act 2001
and for such internal control as the directors determine is necessary to enable the preparation of the
financial report that gives a true and fair view and is free from material misstatement, whether due to
fraud or error.
In preparing the financial report, the directors are responsible for assessing the Group’s ability to
continue as a going concern, disclosing, as applicable, matters relating to going concern and using the
going concern basis of accounting unless the directors either intend to liquidate the Group or to cease
operations, or have no realistic alternative but to do so.
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70
Auditor's responsibilities for the audit of the financial report
Our objectives are to obtain reasonable assurance about whether the financial report as a whole is
free from material misstatement, whether due to fraud or error, and to issue an auditor’s report that
includes our opinion. Reasonable assurance is a high level of assurance, but is not a guarantee that an
audit conducted in accordance with the Australian Auditing Standards will always detect a material
misstatement when it exists. Misstatements can arise from fraud or error and are considered material
if, individually or in the aggregate, they could reasonably be expected to influence the economic
decisions of users taken on the basis of this financial report.
As part of an audit in accordance with the Australian Auditing Standards, we exercise professional
judgment and maintain professional scepticism throughout the audit. We also:
Identify and assess the risks of material misstatement of the financial report, whether due to
fraud or error, design and perform audit procedures responsive to those risks, and obtain audit
evidence that is sufficient and appropriate to provide a basis for our opinion. The risk of not
detecting a material misstatement resulting from fraud is higher than for one resulting from
error, as fraud may involve collusion, forgery, intentional omissions, misrepresentations, or the
override of internal control.
Obtain an understanding of internal control relevant to the audit in order to design audit
procedures that are appropriate in the circumstances, but not for the purpose of expressing an
opinion on the effectiveness of the Group’s internal control.
Evaluate the appropriateness of accounting policies used and the reasonableness of accounting
estimates and related disclosures made by the directors.
Conclude on the appropriateness of the directors’ use of the going concern basis of accounting
and, based on the audit evidence obtained, whether a material uncertainty exists related to
events or conditions that may cast significant doubt on the Group’s ability to continue as a going
concern. If we conclude that a material uncertainty exists, we are required to draw attention in
our auditor’s report to the related disclosures in the financial report or, if such disclosures are
inadequate, to modify our opinion. Our conclusions are based on the audit evidence obtained up
to the date of our auditor’s report. However, future events or conditions may cause the Group
to cease to continue as a going concern.
Evaluate the overall presentation, structure and content of the financial report, including the
disclosures, and whether the financial report represents the underlying transactions and events
in a manner that achieves fair presentation.
Obtain sufficient appropriate audit evidence regarding the financial information of the entities
or business activities within the Group to express an opinion on the financial report. We are
responsible for the direction, supervision and performance of the Group audit. We remain solely
responsible for our audit opinion.
We communicate with the directors regarding, among other matters, the planned scope and timing of
the audit and significant audit findings, including any significant deficiencies in internal control that we
identify during our audit.
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We also provide the directors with a statement that we have complied with relevant ethical
requirements regarding independence, and to communicate with them all relationships and other
matters that may reasonably be thought to bear on our independence, and where applicable, actions
taken to eliminate threats or safeguards applied.
From the matters communicated to the directors, we determine those matters that were of most
significance in the audit of the financial report of the current year and are therefore the key audit
matters. We describe these matters in our auditor’s report unless law or regulation precludes public
disclosure about the matter or when, in extremely rare circumstances, we determine that a matter
should not be communicated in our report because the adverse consequences of doing so would
reasonably be expected to outweigh the public interest benefits of such communication.
Report on the audit of the remuneration report
Opinion on the remuneration report
We have audited the Remuneration Report included in the directors' report for the year ended 30
June 2021.
In our opinion, the Remuneration Report of MGC Pharmaceuticals Limited for the year ended 30 June
2021, complies with section 300A of the Corporations Act 2001.
Responsibilities
The directors of the Company are responsible for the preparation and presentation of the
Remuneration Report in accordance with section 300A of the Corporations Act 2001. Our
responsibility is to express an opinion on the Remuneration Report, based on our audit conducted in
accordance with Australian Auditing Standards.
Ernst & Young
T G Dachs
Partner
Perth
30 September 2021
A member firm of Ernst & Young Global Limited
Liability limited by a scheme approved under Professional Standards Legislation
72
14
ADDITIONAL ASX
INFORMATION
Additional ASX Information
EXCHANGE LISTING
MGC Pharmaceuticals Ltd shares and options are listed on the Australian Securities Exchange under ASX code MXC.
The Company is also listed on the London Stock Exchange via the trading of depositary interests, under code MXC.
SUBSTANTIAL SHAREHOLDERS (HOLDING MORE THAN 5%)
As at 13 September 2021, the Company did not have any substantial shareholders.
CLASS OF SHARES AND VOTING RIGHTS
At 13 September 2021, there were 10,854 holders of 2,385,272,702 ordinary fully paid shares of the Company. The voting
rights attaching to the ordinary shares are in accordance with the Company’s Constitution being that:
a) each Shareholder entitled to vote may vote in person or by proxy, attorney or Representative;
b) on a show of hands, every person present who is a Shareholder or a proxy, attorney or Representative of a shareholder
has one vote; and
c) on a poll, every person present who is a shareholder or a proxy, attorney or Representative of a shareholder shall, in
respect of each fully paid Share held by him, or in respect of which he is appointed a proxy, attorney or Representative,
have one vote for the Share, but in respect of partly paid Shares, shall, have such number of votes as bears the
proportion which the paid amount (not credited) is of the total amounts paid and payable (excluding amounts
credited).
ESCROWED SECURITIES
There are currently 15,151,515 ordinary shares on escrow until 23 November 2021, issued to Cannvalate Pty Ltd as
consideration for the acquisition of Medicinal Cannabis Clinics.
CASH USAGE
Since the time of listing on ASX, the entity has used its cash and assets in a form readily converted to cash that it had at
the time of admission to the official list of ASX in a manner which is consistent with its business objectives.
RANGE OF ORDINARY SHARES AS AT 13 SEPTEMBER 2021
RANGE
1 - 1,000
1,001 - 5,000
5,001 - 10,000
10,001 - 100,000
100,001 and Over
Total
TOTAL HOLDERS
145
301
1,251
7,014
2,143
10,854
SHARES
20,768
1,330,039
10,314,706
298,080,840
2,075,526,349
2,385,272,702
%
0.00
0.06
0.43
12.5
87.01
100.00
The number of shareholders holding less than a marketable parcel is 1,085.
73
UNLISTED SECURITIES AS AT 13 SEPTEMBER 2021
NUMBER
OF
HOLDERS NAME OF HOLDERS HOLDING MORE THAN 20%
SECURITIES
Options exercisable at $0.026
expiring 31/03/2023
Options exercisable at £0.1475
expiring 31/03/2023
Options exercisable at $0.05 expiring
31/08/2023
Options exercisable at $0.06 expiring
31/08/2023
Options exercisable at $0.07 expiring
31/08/2023
Convertible Notes
NUMBER OF
SECURITIES
ON ISSUE
7,692,308
26,440,678
16,300,000
17,500,000
17,500,000
2,475,000
1
1
3
4
4
1
Performance Rights
97,800,000
44
MS NICOLE ANN GODRESSE
JIM NOMINEES LIMITED
CG NOMINEES (AUSTRALIA) PTY LTD
CG NOMINEES (AUSTRALIA) PTY LTD
CG NOMINEES (AUSTRALIA) PTY LTD
MERCER STREET GLOBAL OPPORTUNITY FUND
LLC
CHITTA LU LIMITED
MR BRETT MITCHELL + MRS MICHELLE
MITCHELL +
NUMBER
HELD
7,692,308
26,440,678
14,500,000
14,500,000
14,500,000
2,100,000
32,440,000
32,440,000
TOP 20 SHAREHOLDERS AS AT 13 SEPTEMBER 2021
RANK NAME
NUMBER OF
SHARES
% OF SHARES
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
COMPUTERSHARE CLEARING PTY LTD
HSBC CUSTODY NOMINEES (AUSTRALIA) LIMITED
CITICORP NOMINEES PTY LIMITED
MR GEORGE BISHAY
MERCER STREET GLOBAL OPPORTUNITY FUND LLC
BNP PARIBAS NOMINEES PTY LTD ACF CLEARSTREAM
BNP PARIBAS NOMS PTY LTD
BNP PARIBAS NOMINEES PTY LTD SIX SIS LTD
MR BRETT MITCHELL + MRS MICHELLE MITCHELL
CANNVALATE PTY LTD
THE TRUST COMPANY (AUSTRALIA) LIMITED
CHETCUTI HOLDINGS PTY LTD
SURFIT CAPITAL PTY LTD
MERRILL LYNCH (AUSTRALIA) NOMINEES PTY LIMITED
CS FOURTH NOMINEES PTY LIMITED
MR BRETT MITCHELL + MRS MICHELLE MITCHELL
FADCO INVESTMENTS LIMITED
ANDORYKA HOLDINGS PTY LTD
DR JONATHAN GRUNFELD
J & D PEOS SUPER PTY LTD
861,191,552
115,831,701
41,376,298
36,822,890
34,300,000
27,835,388
24,814,099
19,191,067
17,156,249
15,151,515
12,500,000
12,000,000
11,500,000
11,179,778
8,651,535
8,418,337
6,772,613
6,166,666
6,090,909
5,585,262
36.1
4.86
1.73
1.54
1.44
1.17
1.04
0.8
0.72
0.64
0.52
0.5
0.48
0.47
0.36
0.35
0.28
0.26
0.26
0.23
Total
1,282,535,859
53.75
74
75
MGC Pharmaceuticals Limited ABN 30 116 800 269
1202 Hay Street
West Perth WA 6005
Tel
Email
+61 8 6382 3390
info@mgcpharma.com.au
mgcpharma.com.au
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