Q4 FY25 Quarterly Activities Report & Appendix 4C
Released
Released
Announcement PDF
ASX Announcement
22 July 2025
Q4 FY25 QUARTERLY ACTIVITIES REPORT & APPENDIX 4C
Strategic Focus Drives Record Core Test Sales and Clinical Adoption
Microba Life Sciences Limited (ASX: MAP) (“Microba” or the “Company”), a company at the forefront of microbiome
diagnostics & therapeutics, is pleased to provide a summary of its activities for the quarter ended 30 June 2025.
Key Highlights
Australia: Continued strong sales momentum for MetaXplore
o Record quarterly sales with Q4 test sales 3,451, up 88% vs PCP
o Q4 annualised run-rate of 13,800 tests sold, up 88% vs PCP
o Growth underpinned by a continued increase in the number of
ordering clinicians
o Landmark GI Study Results from over 4,600 patients with 71.4%
identifying actionable results
•
•
•
Australia: MetaPanel adoption continuing to build
o Q4 test sales 266, up 85% vs PCP
o Breakthrough Study Results in over 800 patients, with 20% of
MetaPanel tests positive for a pathogen, and 78% of results often
missed by routine pathology tests
o Multiple new specialist Key Opinion Leader clinicians engaged
Continued growth in core test volumes
4,500
4,000
3,500
3,000
2,500
2,000
1,500
1,000
United Kingdom: Continued strong growth in MetaXplore test sales
o Q4 MetaXplore test sales 429, up 74% QoQ, PCP not applicable
500
o Full market access was achieved at the end of May, with June
0
delivering strong growth underpinned by successful onboarding
and adoption by new ordering clinicians
o MetaXplore tests now represent 66% of GI tests sold in the UK
business at 30 June 2025
MetaXplore (AUS) MetaPanel (AUS) MetaXplore (UK)
o Total supplement sales $1.1m, down 11% vs PCP reflecting
transition due to greater focus on Invivo branded and owned
supplements
• Invivo branded and owned supplements sales $0.68m, up 12% vs PCP, with leading SKU recording multiple record
sales months
Financial Performance 1
•
•
1
2
FY25 Revenue of $15.67m, up 30% vs PCP, and in line with previous guidance1
o Q4 FY25 Total Revenue of $4.2m up 22% QoQ, down 13.5% vs PCP due to discontinued legacy product revenue
Personal Testing and Supplements revenue of $4.1m, up 25.3% QoQ, up 3.8% vs PCP,
Research Testing revenue of $62k, down 92% vs PCP, following transfer to CMC (see ASX Ann. 10/10/24)
o Q4 FY25 Cash receipts of $3.99m, down 5.6% on QoQ, down 14.2% on PCP, due to reduced receipts from
discontinued legacy products & services phasing out across the period.
$14.5m capital raise completed via $12.5m strategic placement and $2m fully underwritten share purchase plan*
•
$11.74m in Cash or Equivalents at 30 June 2025, including $6.05m from Tranche 1 of the placement. A further $8.45m
will settle in August from Tranche 2 of the placement and the fully underwritten SPP*.
•
The Quarterly Investor Webinar will be held at 12:00pm (midday) AEST on Wednesday, 23 July 2025. You can register
and access the webinar via this link: https://ir.microba.com/webinars/4PKExe-q4-fy25-quarterly-investor-webinar
Financials are preliminary and unaudited.
Subject to shareholder approval at the Extraordinary General Meeting (EGM) scheduled for 8 August 2025.
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Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
ASX Announcement
22 July 2025
“We are pleased to report a strong finish to FY25 aligned to our revenue
guidance, with continued growth and clinical adoption of our core tests in
Australia and the United Kingdom. Having almost completed the strategic
transition to focus on these high-value products, we are now seeing the
benefit in accelerating sales momentum. This shift has positioned us for
sustained revenue growth, and coupled with the successful $14.5 million
capital raise, we are well-funded to execute our growth strategy, and path to
regional break-even points in FY26.”
“To further exemplify our progress in completing the product and revenue
transition mix to our core testing products, see the charts on the right showing
quarterly sales grouped by product into 3 categories: Growth, Base and
Legacy.
2,000,000
1,800,000
1,600,000
1,400,000
1,200,000
1,000,000
800,000
600,000
400,000
“For our Growth products, in Australia, MetaXplore maintained its growth
trajectory, achieving a record quarter. This growth was supported by landmark
GI study results from over 4,600 patients, further validating the clinical utility
of this test for lower gastrointestinal disorders. MetaPanel adoption continues
to gradually build, also supported by breakthrough study results showing its
clinical utility gastrointestinal pathogen detection, combined with
engagement from multiple new specialist KOL clinicians driving education and
uptake in this market development phase.”
2,000,000
“In the United Kingdom, MetaXplore is gaining traction and has accelerated
following full market access at the end of May, with record results in June.
800,000
For our Base products, where we expect sales and revenue to remain largely
stable and consistent. Supplement sales dipped slightly for the quarter,
reflecting our transition to more focus on our higher margin Invivo branded (as
opposed to third party distributed products) products where we achieved
strong growth with our top selling PHGG prebiotic supplement.”
For our remaining Legacy products, in the United Kingdom, the migration of
customers from the legacy EcologiX products to MetaXplore is on track with
MetaXplore now representing over half of all GI tests sold in the UK.
We are focused on continuing to accelerate sales of our core testing products
across Australia and the United Kingdom, and are optimistic about our FY26
growth, which we expect to build across the financial year aligned to the
growth profile of FY25 stepping up each quarter aligned to growth in clinician
adoption and higher usage aligned to planned key product feature releases”
GROWTH
MetaXplore & MetaPanel
200,000
0
BASE
Supplements & Intl test partners
1,600,000
1,200,000
400,000
0
2,000,000
LEGACY
Insight, Research & EcologiX
1,600,000
1,200,000
800,000
400,000
0
For our therapeutics business, we moved to finalise all R&D activity, preserve
all core intellectual property for our therapeutic assets, and remain active in
partnering opportunities aligned to upcoming clinical data catalysts in the
sector expected before the end of the calendar year.
With a solid cash position, and intensive focus on growth of our core products
we are confident in our trajectory to capture this initial $25 billion market
opportunity for this major new diagnostic category.”
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announcements and updates, visit ir.microba.com/welcome
Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
ASX Announcement
22 July 2025
KEY HIGHLIGHTS
Landmark GI Study Results from over 4,600 patients
Results were released from the analysis of over 4,600
MetaXplore™ GI Plus test results.
The study demonstrated that MetaXplore™ can support
clinicians to identify and address underlying gut issues that
often go undetected by conventional testing.
In over 70% of cases, the test revealed findings, such as
abnormalities in gut bacteria, signs of infection, markers of
inflammation or insufficiency that could inform targeted
treatment strategies.
Further, two-thirds of MetaXplore™ patients in a separate
study of follow up survey results reported improvement of
symptoms after their care was guided by the test results.
These results highlight the clinical value of MetaXplore™ test results in advancing outcomes for patients with chronic
lower gastrointestinal disorders, highlighting the potential to reshape clinical management of these conditions and set a
new standard of care.
Associate Professor Graham Radford-Smith, a leading gastroenterologist and expert in functional GI disorders, is currently
working with Microba on a clinical utility study of MetaXplore™ in his practice. He commented:
“MetaXplore is a powerful addition to the diagnostic toolbox for patients with persistent gastrointestinal symptoms. It enables
me to objectively identify microbiome dysbiosis, evaluate dietary quality, and direct patients toward evidence-based nutritional
strategies. Importantly, it helps differentiate patients with normal GI and microbial profiles who may benefit from
psychological support rather than further invasive testing or pharmacological escalation.”
MetaPanel Pathogen Study Delivers Breakthrough Results
Results were released from analysis of 889 MetaPanel™ tests
from a patient cohort characterised by long-term
gastrointestinal symptoms, who have not resolved their
condition through routine testing. The data demonstrates the
ability of MetaPanel™ to identify clinically significant
pathogens that are often missed by standard diagnostic
approaches, guide treatment, and achieve symptom
resolution.
•
20.0% of patients test positive for a pathogen that can
cause gastrointestinal infection
•
78.4% of the pathogens detected by MetaPanel are often
missed by routine pathology tests
•
100% of patients treated for a pathogen detected by
MetaPanel experienced complete symptom resolution in an independent study
Associate Professor Michael Wehrhahn, Director of Molecular Biology/Infectious Serology at Douglass Hanly Moir
Pathology, who is leading this study, commented:
“These findings are an important advancement in how we diagnose and treat chronic gastrointestinal symptoms. The
ability of MetaPanel to detect pathogens that evade routine testing — and achieve complete symptom resolution in many
treated cases — highlights its potential to transform patient outcomes.”
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Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
ASX Announcement
22 July 2025
GROWTH
Australia - MetaXplore™ Gastrointestinal Disorder Test
Continued growth momentum for MetaXplore in Australia during Q4 FY25 was driven by strategic clinician education,
focused field sales activity, and ongoing product enhancements, underpinned by an increase in the number of ordering
clinicians.
Tests Sold
Ordering Clinicians
Q4 FY25
3,451
790
vs Q4 FY24 (PCP)
1,835, up 88%
418, up 89%
vs Q3 FY25 (QoQ)
3,225, up 7%
698, up 13%
Australia - MetaPanel™ Gastrointestinal Pathogen Test
Current focus is on development of Gastroenterology specialists which will drive adoption activity in the rest of the
clinician market. Aligned to this, we expect a gradual rate of adoption over the next year, with subsequent years
providing the opportunity for larger volume as our consistent KOL and evidence development work starts to yield results
in routine usage. Dissemination of recent study results, strategic clinician education events, targeted field sales
activities, and KOL led engagement events continue to develop the market and build health care professional awareness
and patient referral confidence in this market development phase.
Tests Sold
Q4 FY25
266
vs Q4 FY24 (PCP)
144, up 85%
vs Q3 FY25 (QoQ)
201, up 32%
United Kingdom - MetaXplore Gastrointestinal Disorder Test
Full market access completed aligned to schedule at the end of May 2025, delivering break-out results for June with 1
month of full-market access captured before the completion of Q4. Strategic clinician education, large industry events,
targeted field sales activities and product enhancements delivered strong growth in Q4 FY25 for MetaXplore in the
United Kingdom, underpinned by a strong increase in number of ordering clinicians on the back of opening full market
access.
MetaXplore Tests Sold
Ordering Clinicians
Q4 FY25
429
162
vs Q4 FY24 (PCP)
Not available
Not available
vs Q3 FY25 (QoQ)
246, up 74%
57, up 184%
BASE
United Kingdom – Nutritional Supplements
Supplement revenues were slightly down this quarter reflecting the transition to a greater focus on our higher margin
Invivo branded and owned supplements vs third party distributed Designs For Health (DFH) branded products. Invivo
branded and owned supplements grew, with strong growth for the hero supplements product, PHGG prebiotic
supplement. Growth was driven by targeted digital campaigns (Google, Instagram), Amazon storefront, and distributor
account management.
Invivo Supplements
Distributed Supplements
(DFH)
Q4 FY25
$0.68m
$0.46m
vs Q4 FY24 (PCP)
$0.61m, up 12%
$0.67m, down 31%
vs Q3 FY25 (QoQ)
$0.63m, up 8%
$0.65m, down 29%
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announcements and updates, visit ir.microba.com/welcome
Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
ASX Announcement
22 July 2025
International Testing Product Partners
Microba has strategically maintained its distribution partnership with SYNLAB in EU and LATAM and Genova in the US.
These relationships are not in our core active markets today (Australia and the United Kingdom –we are focused with
Sonic Healthcare). These strategic relationships continue to be actively maintained aligned to our future European and
United States geographical expansion strategy.
Q4 FY25
$0.33m
SYNLAB & Genova Sales ($)
vs Q4 FY24 (PCP)
$0.30m, up 10%
vs Q3 FY25 (QoQ)
$0.30m, up 11%
LEGACY
United Kingdom – EcologiX Test Range
The migration of customers from the legacy EcologiX products to MetaXplore is on track with MetaXplore now
representing over half of all GI tests sold in the UK. Customers were notified of EcologiX range discontinuation in May25, sales formally close in at the end of July-25, and EcologiX test processing will close in October-25.
EcologiX Tests Sold
Q4 FY25
912
vs Q4 FY24 (PCP)
1,688, down 46%
vs Q3 FY25 (QoQ)
1,323, down 31%
THERAPEUTICS
After a heavy research, development and de-risking phase over the last 5 years for Microba’s Therapeutics business, the
team have now shifted to stop all investment in research and development, whilst maintaining all therapeutic core asset
intellectual property, and focus is now exclusively on partnering.
Microba maintains a competitive advantage in human data driven discovery from the human microbiome and holds
field leading live biotherapeutic assets with deep preclinical and early clinical validation.
Prospective partners are awaiting definitive Phase 1b/2a efficacy data from the live biotherapeutic modality. Two trials
are expected to read out for peer companies before the end of the calendar year. If positive, it is expected that this
could be a key catalyst for transaction activity.
FINANCIALS
Microba achieved unaudited FY25 revenue of $15.67 million, representing 30% growth on FY24 and in line with the
revised guidance of $15.4 – $16.0 million. Q4 FY25 revenue totalled $4.2 million, up 22% QoQ, driven by growth in core
testing products, but down 13.5% vs PCP due to the phased discontinuation of legacy products and services.
Revenue (unaudited) for Q4 FY25 from Personal Testing and Supplements grew to $4.1 million, up 25.2% QoQ and 3.7%
vs PCP, reflecting the increasing contribution of core products. Research Testing revenue declined to $0.06 million
(down 92% vs PCP) following the transfer and discontinuation of this legacy business segment.
Q4 FY25 cash receipts totalled $3.99m, down 5.6% QoQ and 14.2% vs PCP primarily due to reduced receipts from
discontinued legacy products and services which phased out across the period.
Total Operating Cash Outflows for the June 2025 quarter totalled $5.56m, driven by:
•
A $0.39 million increase in manufacturing costs to $2.49 million driven by testing volume growth.
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Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
ASX Announcement
22 July 2025
•
An increase in R&D expenditure to $0.45 million (from $0.35 million in Q3), due to final pre-clinical
Therapeutics study close-out. Therapeutics R&D spend will materially decrease from FY26 onwards.
•
Staff costs increased to $4.4 million (up from $4.1 million in Q3), driven by higher test volumes and one-off
costs from strategic employee reductions associated with the discontinuation of legacy products and strategic
focus.
•
Administrative and corporate expenses were elevated in Q4 compared with Q3 due to the timing of several
large payments and settlement of annual pre-paid invoices.
In FY26 it is planned that overall Total Operating Cash Outflows will be lower than in FY25, aligned to our strategic focus
and regional break-even objectives.
As at 30 June 2025, Microba held $11.74m in cash or equivalents including $6.05m from Tranche 1 of the recent
placement. An additional $8.45m is due to settle in August from Tranche 2 of the placement and the fully underwritten
SPP. The Company also expects to receive approximately $2.5 million under the FY25 R&D Tax Incentive in H1 FY26.
In accordance with Listing Rule 4.7C, payments made during the quarter to related parties and their associates included
in item 6.1 of Appendix 4C was $143,052 and included Director fees.
This announcement has been authorised for release by the Board.
For further information, please contact:
Dr Luke Reid
Chief Executive Officer
luke.reid@microba.com
https://ir.microba.com/welcome
About Microba Life Sciences Limited
Microba Life Sciences is a precision microbiome company driven to improve human health. With world-leading technology
for measuring the human gut microbiome, Microba is driving the discovery and development of novel therapeutics for
major chronic diseases and delivering gut microbiome testing services globally to researchers, clinicians, and consumers.
Through partnerships with leading organisations, Microba is powering the discovery of new relationships between the
microbiome, health and disease for the development of new health solutions. For more information visit www.microba.com
JOIN MICROBA’S INTERACTIVE INVESTOR HUB
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announcements and updates, visit ir.microba.com/welcome
Microba Life Sciences Ltd | ABN 82 617 096 652 | L10, 324 Queen Street, Brisbane QLD 4000 Australia | 1300 974 621
Rule 4.7B
Appendix 4C
Quarterly cash flow report for entities
subject to Listing Rule 4.7B
Name of entity
Microba Life Sciences Limited, and controlled entities
ABN
Quarter ended (“current quarter”)
82 617 096 652
30 June 2025
Consolidated statement of cash flows
Current quarter
$A’000
1.
Cash flows from operating activities
1.1
Receipts from customers
1.2
Payments for
Year to date
$A’000
3,996
17,170
(452)
(1,882)
(2,485)
(8,988)
(c) advertising and marketing
(395)
(1,315)
(d) leased assets
(263)
(992)
(e) staff costs
(4,435)
(16,074)
(f)
(1,743)
(5,853)
-
-
(a) research and development
(b) product manufacturing and operating
costs
administration and corporate costs
1.3
Dividends received (see note 3)
1.4
Interest received
234
828
1.5
Interest and other costs of finance paid
(15)
(86)
1.6
Income taxes paid
-
(5)
1.7
Government grants and tax incentives
-
5,993
1.8
Other (provide details if material)
-
-
1.9
Net cash from / (used in) operating
activities
(5,558)
(11,204)
2.
Cash flows from investing activities
2.1
Payments to acquire or for:
(a) entities
-
-
(b) businesses
-
-
(27)
(1,677)
-
-
(732)
(2,412)
-
-
(c) property, plant and equipment
(d) investments
(e) intellectual property
(f)
other non-current assets
ASX Listing Rules Appendix 4C (17/07/20)
+ See chapter 19 of the ASX Listing Rules for defined terms.
Page 1
Appendix 4C
Quarterly cash flow report for entities subject to Listing Rule 4.7B
Consolidated statement of cash flows
2.2
Current quarter
$A’000
Year to date
$A’000
Proceeds from disposal of:
(a) entities
-
-
(b) businesses
-
-
(c) property, plant and equipment
-
-
(d) investments
-
-
(e) intellectual property
-
-
(f)
-
-
other non-current assets
2.3
Cash flows from loans to other entities
-
-
2.4
Dividends received (see note 3)
-
-
2.5
Other (provide details if material)
-
-
2.6
Net cash from / (used in) investing
activities
(759)
(4,089)
3.
Cash flows from financing activities
3.1
Proceeds from issues of equity securities
(excluding convertible debt securities)
6,046
6,046
3.2
Proceeds from issue of convertible debt
securities
-
-
3.3
Proceeds from exercise of options
-
-
3.4
Transaction costs related to issues of
equity securities or convertible debt
securities
(385)
(385)
3.5
Proceeds from borrowings
410
1,707
3.6
Repayment of borrowings
(202)
(906)
3.7
Transaction costs related to loans and
borrowings
-
-
3.8
Dividends paid
-
-
3.9
Other (provide details if material)
-
-
3.10
Net cash from / (used in) financing
activities
5,869
6,462
4.
Net increase / (decrease) in cash and
cash equivalents for the period
4.1
Cash and cash equivalents at beginning of
period
12,412
20,890
4.2
Net cash from / (used in) operating
activities (item 1.9 above)
(5,558)
(11,204)
4.3
Net cash from / (used in) investing activities
(item 2.6 above)
(759)
(4,089)
4.4
Net cash from / (used in) financing activities
(item 3.10 above)
5,869
6,462
ASX Listing Rules Appendix 4C (17/07/20)
+ See chapter 19 of the ASX Listing Rules for defined terms.
Page 2
Appendix 4C
Quarterly cash flow report for entities subject to Listing Rule 4.7B
Consolidated statement of cash flows
Current quarter
$A’000
Year to date
$A’000
4.5
Effect of movement in exchange rates on
cash held
(222)
(317)
4.6
Cash and cash equivalents at end of
period
12,412
12,412
5.
Reconciliation of cash and cash
equivalents
Current quarter
$A’000
Previous quarter
$A’000
at the end of the quarter (as shown in the
consolidated statement of cash flows) to the
related items in the accounts
5.1
Bank balances
10,742
11,412
5.2
Call deposits
-
-
5.3
Bank overdrafts
-
-
5.4
Other (provide details)*
1,000
1,000
5.5
Cash and cash equivalents at end of
quarter (should equal item 4.6 above)
11,742
12,412
*A term deposit of $1,000,000 was classified as restricted cash as stipulated under the NovaSeqX funding agreement (referred
to at Section 7 of this document). The term deposit will be held for the duration of the agreement (36 months). The term deposit
rolls over every 3 months and is subject to an interest rate review on rollover.
6.
Payments to related parties of the entity and their
associates
6.1
Aggregate amount of payments to related parties and their
associates included in item 1
6.2
Aggregate amount of payments to related parties and their
associates included in item 2
Current quarter
$A'000
(143)
Note: Payments included in item 6.1 above relate to Director Fees and Consulting Fees paid to Directors of Microba Life
Sciences Limited during the period.
ASX Listing Rules Appendix 4C (17/07/20)
+ See chapter 19 of the ASX Listing Rules for defined terms.
Page 3
Appendix 4C
Quarterly cash flow report for entities subject to Listing Rule 4.7B
7.
Financing facilities
Note: the term “facility’ includes all forms of financing
arrangements available to the entity.
Add notes as necessary for an understanding of the
sources of finance available to the entity.
Total facility
amount at quarter
end
$A’000
Amount drawn at
quarter end
$A’000
7.1
Loan facilities
-
-
7.2
Credit standby arrangements
-
-
7.3
Other (please specify)
(1,215)
(1,215)
7.4
Total financing facilities
(1,215)
(1,215)
7.5
Unused financing facilities available at quarter end
7.6
Include in the box below a description of each facility above, including the lender, interest
rate, maturity date and whether it is secured or unsecured. If any additional financing
facilities have been entered into or are proposed to be entered into after quarter end,
include a note providing details of those facilities as well.
0
Insurance Premium Funding Agreement: An unsecured insurance premium funding arrangement
was entered into to finance the Group's annual insurance premiums. The balance originally drawn
was $409k on 25 May 2024, the balance owing at quarter end was $316k. The funding arrangement is
repayable over 10 equal monthly instalments, with a fixed interest rate of 2.57%.
NovaSeqX Plus Funding Agreement: A funding arrangement was entered into to finance the
purchase of a state-of-the-art Illumina NovaSeqX Plus sequencing machine. The funding is secured
against the machine. The balance originally drawn was $1.298m on 30 July 2024, the balance owing
at quarter end was $897k. The funding arrangement is repayable over 36 equal monthly instalments,
with a fixed interest rate of 8.52%.
8.
Estimated cash available for future operating activities
$A’000
8.1
Net cash from / (used in) operating activities (item 1.9)
(5,558)
8.2
Cash and cash equivalents at quarter end (item 4.6)
11,742
8.3
Unused finance facilities available at quarter end (item 7.5)
8.4
Total available funding (item 8.2 + item 8.3)
8.5
Estimated quarters of funding available (item 8.4 divided by
item 8.1)
0
11,742
2.1
Note: if the entity has reported positive net operating cash flows in item 1.9, answer item 8.5 as “N/A”. Otherwise, a
figure for the estimated quarters of funding available must be included in item 8.5.
8.6
If item 8.5 is less than 2 quarters, please provide answers to the following questions:
8.6.1
Does the entity expect that it will continue to have the current level of net operating
cash flows for the time being and, if not, why not?
N/A
8.6.2
Has the entity taken any steps, or does it propose to take any steps, to raise further
cash to fund its operations and, if so, what are those steps and how likely does it
believe that they will be successful?
N/A
ASX Listing Rules Appendix 4C (17/07/20)
+ See chapter 19 of the ASX Listing Rules for defined terms.
Page 4
Appendix 4C
Quarterly cash flow report for entities subject to Listing Rule 4.7B
8.6.3
Does the entity expect to be able to continue its operations and to meet its business
objectives and, if so, on what basis?
N/A
Note: where item 8.5 is less than 2 quarters, all of questions 8.6.1, 8.6.2 and 8.6.3 above must be answered.
Compliance statement
1
This statement has been prepared in accordance with accounting standards and policies
which comply with Listing Rule 19.11A.
2
This statement gives a true and fair view of the matters disclosed.
Date:
22 July 2025
Authorised by: The Board of Directors
(Name of body or officer authorising release – see note 4)
Notes
1.
This quarterly cash flow report and the accompanying activity report provide a basis for informing the market about the
entity’s activities for the past quarter, how they have been financed and the effect this has had on its cash position. An
entity that wishes to disclose additional information over and above the minimum required under the Listing Rules is
encouraged to do so.
2.
If this quarterly cash flow report has been prepared in accordance with Australian Accounting Standards, the definitions
in, and provisions of, AASB 107: Statement of Cash Flows apply to this report. If this quarterly cash flow report has been
prepared in accordance with other accounting standards agreed by ASX pursuant to Listing Rule 19.11A, the
corresponding equivalent standard applies to this report.
3.
Dividends received may be classified either as cash flows from operating activities or cash flows from investing activities,
depending on the accounting policy of the entity.
4.
If this report has been authorised for release to the market by your board of directors, you can insert here: “By the board”.
If it has been authorised for release to the market by a committee of your board of directors, you can insert here: “By the
[name of board committee – eg Audit and Risk Committee]”. If it has been authorised for release to the market by a
disclosure committee, you can insert here: “By the Disclosure Committee”.
5.
If this report has been authorised for release to the market by your board of directors and you wish to hold yourself out as
complying with recommendation 4.2 of the ASX Corporate Governance Council’s Corporate Governance Principles and
Recommendations, the board should have received a declaration from its CEO and CFO that, in their opinion, the financial
records of the entity have been properly maintained, that this report complies with the appropriate accounting standards
and gives a true and fair view of the cash flows of the entity, and that their opinion has been formed on the basis of a
sound system of risk management and internal control which is operating effectively.
ASX Listing Rules Appendix 4C (17/07/20)
+ See chapter 19 of the ASX Listing Rules for defined terms.
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