Q1 FY25 Quarterly Activities Report & Appendix 4C
Released
Released
Announcement PDF
ASX Announcement
29 October 2024
Q1 FY25 QUARTERLY ACTIVITIES REPORT & APPENDIX 4C
Continued Strong Sales & Clinical Adoption in Australia. First Orders of MetaXplore
in the United Kingdom, Post Quarter End.
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 September 2024.
Key Highlights
•
•
Financial Performance 1
• Cash receipts of $5.07m, up 184% vs Previous Corresponding
Period (PCP)
• Revenue of $3.65m, up 239% vs PCP
Personal Testing & Supplements revenue of $3.39m, up
317% vs PCP
Research Testing revenue of $0.26m, down 1% vs PCP
Testing Business
• Australia: Continued strong sales momentum for MetaXplore
Q1 annualised run rate of 7,328 MetaXplore tests sold
Strong start in Q2, with October a record sales month as
of the 25th, with a week left in the month
•
•
1
Australia: MetaPanel sales continuing to build across all
major states through Sonic Healthcare (ASX: SHL) network.
MetaPanel presented at Australian Gastroenterology Week
2024 (hosted by GESA)
MetaXplore Australian Sales Annualised Run Rate
8000
7000
6000
5000
4000
3000
2000
1000
0
2HFY23
1HFY24
2HFY24
Q1FY25
United Kingdom: Invivo Clinical transitioning to a new growth phase in H2 FY25
Sales force doubled at end of quarter aligned to the growth strategy
MetaXplore access commenced in October 2024 with first orders already received
•
Accelerating Growth Through Strategic Appointments
Eric Davis, Ex Abbott and Cochlear appointed as Chief Growth Officer
Chris Saad, Ex Uber appointed as Chief Product Officer
•
$16.4m in Cash or Equivalents at 30 September 2024, with $6.0m expected from Microba’s FY24 R&D
Tax Incentive, which was lodged during the quarter and is expected to be received in Q2 FY25
•
The Quarterly Investor Video Presentation is now available via the Company’s Investor Hub where
investors and stakeholders can ask questions of management via this link
https://ir.microba.com/announcements
Financials are preliminary and unaudited
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ASX Announcement
29 October 2024
Commenting on the quarter, Microba’s CEO, Dr Luke Reid, said:
“We continued to deliver positive sales momentum for our testing business led by MetaXplore test sales in Australia”
“In the United Kingdom, Q1 results were impacted through an intentional focus of the team on actively preparing for
MetaXplore access in the UK across August and September. Through that focus, the team successfully achieved first
MetaXplore orders in the UK in October under an Early Access Program to key clinician accounts, and doubled the size of the
sales force setting up for growth and full market access in 2025”
“Microba’s Therapeutic Development Programs continue to advance aligned to plan. Actively advancing MAP 315 to a Phase
2 clinical trial to demonstrate clinical efficacy. Growth in data for our Immuno-Oncology program. Generating further data
supporting the leads for our Autoimmune Program. Active in our global partnering efforts. The potential of our groundbreaking
therapeutic platform, innovative pipeline, and assets is incredibly exciting for patients and our shareholders.
“We continue to attract world class talent to spearhead our growth momentum. The attraction of this calibre of top tier talent
is testament to the quality of the organisation we have built, the significance of the global opportunity, and our conviction for
future success and impact of Microba”
“Microba is intensively focused on executing its testing and therapeutic business strategies. This quarter’s continued strong
results demonstrate the traction we are gaining in the market, giving us great confidence and excitement for the growth ahead
with an expected strong close to H1, and continued growth acceleration into H2.”
TESTING BUSINESS
Strategic transfer of Research Services Business Unit
On 10 October 2024, Microba announced it had entered into an agreement for the strategic transfer of its non-core
Research Services business unit to Clinical Microbiomics A/S (CMC), a Denmark headquartered, global contract research
organisation (CRO) specialising in microbiome genetic and metabolic analysis to industry and academic institutions.
The transfer of Microba’s Research Services business unit will allow Microba to allocate 100% of its testing operations
and business development resources to the growth of its core diagnostic microbiome testing business. This reinforces
Microba’s commitment to growth through intensive focus and operational excellence.
Under the terms of the Transfer Agreement, Microba will receive:
• retained revenue payable to Microba from existing contracts assigned to CMC
• commission payments for existing contracts assigned to CMC to the extent performed by CMC for up to a fouryear period after completion;
• commission payments for new contracts with existing customers transitioned to CMC to the extent performed
by CMC for up to a four-year period after completion, and new customers referred by Microba to CMC; and
• potential milestone payments across the next four financial years.
As a result of the above, the potential revenue to be received by Microba under the Transfer Agreement is up to
$3,000,000 across the next four financial years.
Refer to full announcement here
Refer to video with Dr Luke Reid discussing strategic rationale here
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ASX Announcement
29 October 2024
MetaXplore™ Gastrointestinal Disorder Test
Strategic clinician education and sales activities in Australia delivered continued growth. This growth was
represented in tests sales and by growth in ordering clinicians counteracting reduced sales from high volume
accounts impacted by the winter school holiday period.
Sales & Health Care Professional (HCP) Accounts:
Despite the seasonal softness of revenues in Q1 vs Q4 driven by July & September school holiday periods in
Australia, MetaXplore saw strong growth compared to the prior comparable period.
Tests Sold
Ordering Clinicians
Q1 FY25
1,832
487
vs Q1 FY24 (PCP)
913, up 101%
269, up 81%
vs Q4 FY24 (QoQ)
1,835, 0%
414, up 17%
Growth strategy
•
•
•
•
Targeted sales and marketing activities focused on high prescribing potential clinicians
Clinician education
Key Opinion Leader engagement
Utility studies and publications
Commercial Opportunity:
MetaXplore™ is the most comprehensive test available to support diagnosis and management of functional
gastrointestinal disorders. It is estimated that total addressable market for the MetaXplore test in the United States
alone is over US $9.5B 2.
MetaPanel™ - Gastrointestinal Pathogen Test
Through Q1 FY25, further progress was made to bring MetaPanel™, a world-first diagnostic test, to healthcare
professionals and patients nationwide across Australia. Doctor referrals and sales continuing to build across the country.
In collaboration with Sonic Healthcare (ASX: SHL), the team are continuing to drive active KOL engagement, evidence
generation activities and utility publications to support clinician adoption.
National Market Development:
Assoc. Prof. Michael Wehrhahn from Douglass Hanly Moir, the Sonic Healthcare NSW branch, presented on "An early
review of MetaPanel™ a Diagnostic Metagenomic Gastrointestinal Pathogen Assay" to a well-attended workshop
during Australian Gastroenterology Week 2024 hosted by the Gastroenterological Society of Australia (GESA). This is
the leading event of the year for Gastroenterologists.
This event was supported by direct sales activity in Adelaide, seeing the Microba team collaborate with Sonic’s SA
branch, Clinpath, across 20+ clinic visits totalling direct contact with 70+ clinicians.
Early Adoption and Sales:
Doctor referrals and sales continuing to build across the country, focused around the major east coast states New
South Wales, Victoria and Queensland. The sales strategy remains focused on gastroenterology specialists and
general practitioners (GPs). Through executing direct clinician engagement strategies, growing KOL relationships,
2
Assessment of Medicare claims analysis for specific ICD codes related to people with Pain, Bloating or diagnosed with Irritable Bowel Syndrome in the
absence of diarrhea in the United States. Estimated Private and Medicaid numbers extrapolated from Medicare claims analysis. Test pricing assumes
minimum of US $416.78 (aligned to CPT code 57507) for the US, however it is expected that higher pricing opportunity may be available with strong clinical
utility data.
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ASX Announcement
29 October 2024
active clinical utility studies and publications together with the Sonic Healthcare team, we expect adoption to
translate into meaningful sales volume and revenues in FY25.
Commercial Opportunity:
MetaPanel™ is a world-first NATA accredited test for diagnosing gastrointestinal pathogens. It is the most
comprehensive gastrointestinal pathogen test available detecting both common and difficult-to-identify pathogens
capable of causing infection. It is estimated that the total global addressable market for the MetaPanel test is over
US $9B 3.
United Kingdom business, Invivo Clinical
The fundamental investment thesis of the Invivo Clinical acquisition was the ability to accelerate Microba’s entry of its
world leading MetaXplore™ test into the United Kingdom through an established team and customer base.
The UK market demand and anticipation for access to MetaXplore has been compelling since the acquisition was
announced, and the team have now commenced MetaXplore testing access in the UK in October with first orders
already received, setting up for full market access in 2025.
Supporting the UK growth strategy, the Invivo sales force was doubled at the end of the quarter.
Sales & HCP Accounts:
The team's focus on executing the transition to MetaXplore had a temporary impact on EcologiX sales and clinician
numbers during the quarter, coupled with the seasonal softness reflective of the UK summer holidays. Pleasingly,
during October, the Invivo business is trading in line with expectations, and testing and supplements sales are ahead
of September, back in line with non-summer months. This focus and investment are expected to translate into
growth from MetaXplore sales in H2 FY25.
Sales
Tests Sold
Supplements Sold
Ordering Clinicians
Q1 FY25
$2.1m
1,740
31,944
771
vs Q1 FY24 (PCP)
$2.3m, down 5%
2013, down 14%
30,846, up 4%
784, down 2%
vs Q4 FY24 (QoQ)
$2.2m, down 4%
1,934, down 10%
31,833, up 0.5%
826, down 7%
Growth strategy
Stage 0 – Complete, expected to impact results in Q3 FY25
Stage 0 Strategy: Bolster sales resourcing for the UK team with recruitment of new talent and experience to unlock
latent growth potential
• Field sales force doubled
Stage 1 – Commenced, expected to impact results in H2 FY25
Stage 1 Strategy: Launch Microba’s MetaXplore™ product into the UK to drive testing growth
• Early Access Program commenced providing select clinician accounts with access to order MetaXplore, and
first orders already received.
• This Early Access Program will be progressively opened to more clinicians over the months ahead, supporting
full market access in 2025
3
Assessment of Medicare claims analysis for specific ICD codes related to people with Diarrhea of Unknown Etiology who receive molecular testing for
gastrointestinal pathogens in the United States (US). Estimated US private and Medicaid patient numbers extrapolated from Medicare claims analysis.
Estimated Australia (AU), United Kingdom (UK), Germany (DE), Italy (IT), Spain (ES) and France (FR) numbers extrapolated from the US data based on
published prevalence and regional pathogen panel testing information. Test pricing assumes minimum of US $416.78 (aligned to CPT code 57507) for the
US, and pricing for other countries based on Gastrointestinal panel pricing predicates in each country. This is viewed to be the minimum with the top
pricing predicate at US $2126.20.
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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
29 October 2024
THERAPEUTICS BUSINESS
Inflammatory Bowel Disease Program – Advancing MAP 315 for Phase 2
The role of the microbiome in health and disease continues to draw widespread interest from both consumers and the
scientific community.
During the quarter, further progress was made to advance lead drug candidate MAP 315 for a Phase 2 clinical trial.
Partnering efforts are active.
Phase 2 trial plans
Further progress was made over the quarter to prepare for a Phase 2 clinical trial with regulatory and manufacturing
(CMC) activities towards an investigation new drug (IND) submission.
Commercial Opportunity
In December 2023 Microba successfully completed a Phase 1, first in human clinical trial for lead drug candidate
MAP 315.
Preclinical characterisation data, together with the Phase 1 clinical study results and feedback from Microba’s
medical advisory board provide strong positive support for continuing to advance the clinical development of MAP
315 for the treatment of UC.
MAP 315 is being developed for the treatment of UC, a debilitating form of Inflammatory Bowel Disease (IBD) with
>50% of patients unable to achieve sustained remission with current standard of care. The market for UC treatment
was valued at US$7.5b in 2020 and is forecast to grow to US$10.8b by 2030 4.
Microba’s novel drug candidate MAP 315 was originally identified using the Company’s data-driven Therapeutic
Platform, demonstrating that this previously unidentified novel bacterial species is commonly observed in healthy
individuals but consistently deficient in individuals with IBD, and in particular UC. Subsequent pre-clinical
investigation of MAP 315 through both in vitro and in vivo models demonstrated that MAP 315 promotes epithelial
restitution and mucosal healing – biological activities that are associated with disease remission but not adequately
addressed through existing therapies. MAP 315 provides a compelling commercial opportunity to fill a key gap in the
current standard of care for UC treatment and represents a potential novel treatment paradigm for patients living
with this debilitating disease.
Immuno-Oncology Program – Clinical data and sample set grown to over 4,500 patients
During the quarter Microba’s clinical data and sample set was grown to over 4,500 patients. These additional clinical
insights provide a powerful data package in support of potential future clinical development.
Data growth
Through the national Precision Oncology Screening Platform Enabling Clinical Trials (PrOSPeCT) study 5 Microba is
capturing a large and diverse bank of patient specimens for cancer patients receiving treatment and enrolled in
clinical trials. This has quickly grown to over 3,500 patient samples and is expected to be one of the largest clinical
specimen resources with respect to the microbiome and cancer treatment. This resource adds to more than 1,000
patient samples Microba has previously analysed from internally recruited and published studies.
4 https://www.nature.com/articles/d41573-021-00194-5 , https://www.alliedmarketresearch.com/ulcerative-colitis-market
5
https://www.omico.com.au/prospect/
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ASX Announcement
29 October 2024
Commercial Opportunity
This program is targeting the development of a therapeutic to improve response rates in cancer patients receiving
immune checkpoint inhibitor (ICI) therapy. Global ICI sales continue to grow, with Merck announcing sales of the
market-leading drug Keytruda of US$25b for calendar year 2023 6.
There is an increasing body of literature supporting a key role for the microbiome in cancer 7. Cancer
immunotherapy, and more specifically ICIs have become standard of care for a range of tumour types. However,
despite their impact on cancer treatment, up to 70% of patients do not respond to these drugs 8, 9 leaving a large,
underserved patient population. Differences in the microbiomes of responders and non-responders to ICI treatment
have been observed in international studies, and treatment of the microbiome using faecal microbiome transplants
has demonstrated the ability to turn ICI non-responders into responders 10, 11.
Microba has compiled a clinical dataset of over 1,000 individuals treated with ICIs from prospective recruited studies
and published human clinical trial data. Using the Company’s data-driven Therapeutic Platform, this has enabled the
Company to identify organisms that are commonly observed in ICI responders, but consistently deficient in ICI nonresponders Subsequent pre-clinical investigation of these leads through both in vitro models and in vivo animal
models has demonstrated that these organisms induce specific and targeted immune responses, and are able to
significantly reduce tumour burden. A microbiome-based adjuvant therapy that increases response to these drugs
has the potential to become standard of care across a range of cancers, and therefore represents a substantial
commercial opportunity for Microba.
Autoimmune Disease Program – Successful completion of discovery program
During the quarter, leads from the discovery program were advanced through multiple pre-clinical validation models
confirming their disease relevant activity. In addition, both internal work and external autoimmune expert engagement
has advanced study plans towards selection of final target indications.
Pre-clinical validation
The 6 lead strains from the discovery program completed in Q4 were advanced through studies to examine impact
on gut barrier integrity and JAK/STAT pathway inhibition, confirming their disease relevant activity. In addition, the
strains were further characterised for manufacturability and safety.
Commercial Opportunity
In June 2024, Microba completed its lead discovery program in partnership with Ginkgo Bioworks (NYSE: DNA)
identifying 6 leads which demonstrate significant Autoimmune Disease relevant activity.
The data generated through the discovery program provides strong biological validation for further investment in
these assets to move into the next stage of development.
The goal of this program is to discover and develop novel treatments for autoimmune diseases such as lupus,
psoriatic arthritis and certain autoimmune liver diseases. Microba’s Autoimmune Disease program was established in
partnership with Ginkgo Bioworks (NYSE: DNA) in FY22 following Ginkgo’s strategic investment into Microba’s IPO.
Both parties in collaboration committed to a 2-year drug discovery program principally targeting autoimmune
disorders. The partnership brought together Microba’s unique ability to identify and isolate human gut bacteria
associated with health together with the high-throughput microbial screening capabilities of Ginkgo, creating a
powerful drug discovery workflow.
6 https://www.merck.com/news/merck-announces-fourth-quarter-and-full-year-2023-financial-results/
7
Sepich-Poore e al. (2021). The microbiome and human cancer. DOI: 10.1126/science.abc4552.
8 Leonardi et al. (2020). International Journal of Oncology. DOI: 10.3892/ijo.2020.5088.
9 Wolchok et al. (2017). New England Journal of Medicine. DOI: 10.1056/NEJMoa1709684.
10 Baruch et al. (2020). Science. DOI: 10.1126/science.abb5920.
11
Davar et al. (2021). Science. DOI: 10.1126/science.abf3363.
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ASX Announcement
29 October 2024
Functional changes in the microbiome have been unequivocally linked to a broad range of autoimmune disease 12 13
Autoimmune diseases are a family of more than 80 chronic and often life-threatening illnesses, which occur when
the body’s own immune system attacks the body’s healthy cells, tissues and organs. Autoimmune conditions now
impact around 5% of the population and their prevalence is rising 14. The global market for autoimmune disease
treatments was estimated to be US$198b in 2023 and forecast to grow to US$288b by 2028 15. This program
represents a compelling opportunity to identify a next generation of autoimmune therapeutics from the human
microbiome.
Team appointments
Supporting our continued growth momentum, a number of recent appointments have been made.
Appointment of Chief Growth Officer – Eric Davis
Eric brings 35 years of experience in global commercial leadership roles across strategic planning, new product
innovation, marketing and sales. Eric has led high-performance teams at Cochlear and Abbott, driving numerous
global product launches and significant revenue growth. Notably he played an instrumental role in the world’s most
successful medical device, the continuous glucose monitor Freestyle Libre, now generating over $5B in annual sales
for Abbott. Eric is leading the next phase of Microba’s global medical diagnostics go-to-market strategy and growth.
Appointment of Chief Product Officer – Chris Saad
Chris is a renowned product leader with 25 years experience building high-growth companies in Australia and Silicon
Valley. A sought-after advisor globally in product leadership and organisation design, product strategy and product
management. Notably, Chris was a product leader at Uber during its critical growth years.
Financial Update
Unaudited revenue for the September 2024 quarter totalled $3.65m, representing 239% growth vs PCP with Personal
Testing & Supplements up 316% to $3.39m, and Research Testing down 1% to $0.26m. Cash receipts for the September
2024 quarter totalled $5.07m, up 184% vs PCP.
As at 30 September 2024, Microba had $16.4m in cash or equivalents, which does not include the approximately $6m
relating to the Company’s FY24 R&D Tax Incentive which was lodged during the quarter and is expected to be received in
H1 FY25.
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 $164,574 and included Director fees.
This announcement has been authorised for release by the Board.
12
Miyauchi, Eiji, et al. "The impact of the gut microbiome on extra-intestinal autoimmune diseases." Nature Reviews Immunology 23.1 (2023): 9-23.
De Luca, F. and Shoenfeld, Y. The microbiome in autoimmune diseases. Clin Exp Immunol. (2019). https://doi.org/10.1111/cei.13158.
14 Fugger, L.et al. Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases. Cell. (2020).
https://doi.org/10.1016/j.cell.2020.03.007https://doi.org/10.1016/j.cell.2020.03.007.
15 https://www.prnewswire.com/news-releases/global-autoimmune-treatment-market-soars-to-288-32-billion-by-2028--driven-by-a-7-72-cagr-from-2023-301909189.html
13
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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
29 October 2024
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
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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 September 2024
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
5,067
5,067
(520)
(520)
(2,159)
(2,159)
(c) advertising and marketing
(260)
(260)
(d) leased assets
(241)
(241)
(e) staff costs
(3,902)
(3,902)
(f)
(1,798)
(1,798)
-
-
(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
240
240
1.5
Interest and other costs of finance paid
(24)
(24)
1.6
Income taxes paid
(5)
(5)
1.7
Government grants and tax incentives
-
-
1.8
Other (provide details if material)
-
-
1.9
Net cash from / (used in) operating
activities
(3,602)
(3,602)
2.
Cash flows from investing activities
2.1
Payments to acquire or for:
(a) entities
-
-
(b) businesses
-
-
(1,387)
(1,387)
-
-
(520)
(520)
-
-
(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
(1,907)
(1,907)
3.
Cash flows from financing activities
3.1
Proceeds from issues of equity securities
(excluding convertible debt securities)
-
-
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
-
-
3.5
Proceeds from borrowings
1,298
1,298
3.6
Repayment of borrowings
(253)
(253)
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
1,046
1,046
4.
Net increase / (decrease) in cash and
cash equivalents for the period
4.1
Cash and cash equivalents at beginning of
period
20,890
20,890
4.2
Net cash from / (used in) operating
activities (item 1.9 above)
(3,602)
(3,602)
4.3
Net cash from / (used in) investing activities
(item 2.6 above)
(1,907)
(1,907)
4.4
Net cash from / (used in) financing activities
(item 3.10 above)
1,046
1,046
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
4.5
Effect of movement in exchange rates on
cash held
4.6
5.
Current quarter
$A’000
Year to date
$A’000
(1)
(1)
Cash and cash equivalents at end of
period
16,426
16,426
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
15,426
5.2
Call deposits
5.3
Bank overdrafts
5.4
Other (provide details)*
1,000
5.5
Cash and cash equivalents at end of
quarter (should equal item 4.6 above)
16,426
20,890
20,890
*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 rollov
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