Exscientia Business and Financial Update for the Full Year 2022
Exscientia plc (NASDAQ: EXAI) announced substantial developments in its pipeline and partnerships, as well as financial results for Q4 and FY 2022. Key highlights include a major collaboration with Sanofi, initiation of the Phase 1/2 IGNITE study of A2A receptor antagonist EXS21546, and the entry of EXS4318 into clinical trials by Bristol Myers Squibb. Financially, revenue for FY 2022 was $32.9 million, slightly down from $33.0 million in FY 2021. R&D expenses surged to $155.6 million, reflecting investments in the pipeline. The company ended 2022 with $610.9 million in cash and cash equivalents, down from $678.9 million in 2021.
- Initiated IGNITE Phase 1/2 study of EXS21546 with up to 110 patient enrollment.
- Bristol Myers Squibb initiated first-in-human study of EXS4318.
- Received $117.8 million in cash inflows from collaborations, up from $85.3 million in 2021.
- Opened a new state-of-the-art lab in Vienna to enhance research capabilities.
- R&D expenses for FY 2022 increased significantly to $155.6 million from $53.2 million in 2021.
- Net operating cash outflows were $73.1 million, compared to net inflows of $8.1 million in 2021.
- Total equity decreased to $578.3 million in 2022 from $684.5 million in 2021.
Recent developments in the Company’s pipeline, collaborations, and operations as well as financial results for the fourth quarter and full year 2022 are summarised below.
"2022 was marked by significant milestones for
Recent Highlights
Internal pipeline
-
In
March 2023 ,Exscientia highlighted two new differentiated precision oncology programmes in IND-enabling studies; EXS74539 ('539), a reversible and brain penetrant LSD1 inhibitor and EXS73565 ('565), an allosteric MALT1 protease inhibitor -
In
November 2022 ,Exscientia initiated IGNITE, a Phase 1/2 study of its A2A product candidate, ‘546, with the first patient expected to be enrolled in the first half of 2023- The trial is examining the safety, efficacy, pharmacokinetics and pharmacodynamics of ‘546 when used in combination with anti-PD-1 therapy in renal cell carcinoma (RCC) and non-small cell lung cancer (NSCLC), and will enrol up to 110 patients
-
At the ESMO Immuno-Oncology Annual Congress in
December 2022 ,Exscientia presented new data on the development of a novel biomarker to identify patients more likely to respond to ‘546 and to explore the relationship to potential impact of adenosine on PD-1 inhibitor response:- The study identified a novel patient selection multi-gene transcript signature, the adenosine burden score (ABS)
- The ABS was shown to outperform other published adenosine signatures and indicated that reducing adenosine using ‘546 could enhance the efficacy of cancer treatments. These findings will be further explored in the IGNITE study
-
Exscientia anticipates enrolling the first patient in a Phase 1/2 trial for its CDK7 inhibitor, GTAEXS617 (‘617), in the first half of 2023 -
Four posters will be presented at AACR from
April 14-19, 2023 , highlighting data from the ‘546 and ‘539 programmes as well as data from the Company's precision medicine platform leveraged for biomarker and target discovery
Partnered programmes
-
In
February 2023 ,Exscientia announced a first-in-human study of ‘4318, the first immunology & inflammation candidate designed byExscientia and in-licensed by Bristol Myers Squibb- ‘4318 is a potentially first-in-class potent and selective PKC-theta inhibitor and is Exscientia’s fourth molecule to enter the clinic
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Bristol Myers Squibb will oversee the clinical and commercial development and
Exscientia is eligible for milestone payments and, if approved, tiered royalties on net product sales
Collaboration with leading European medical centre
-
In
March 2023 ,Exscientia and Charité – UniversitätsmedizinBerlin (Charité) announced an academic collaboration to utilise Exscientia’s functional drug testing platform in haematological cancers- Charité will establish a biobank of viably cryopreserved blood, bone marrow and lymph node tissues to support technology development, clinical and future translational research
- Partnership will further validate Exscientia’s platform to predict drug resistances and standard of care responses in haematological cancers
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Exscientia opened a new, 50,000 square foot state-of-the-art laboratory inVienna, Austria to further advance its primary patient sample precision medicine and translational research platforms.Exscientia's approach integrates complex multi-omics and functional data into its AI-driven platform, with the aim of increasing clinical success through better preclinical models - In 2022, the Company expanded its next generation sequencing (NGS), multi-omics platform, patient tissue collaborations and precision medicine capabilities
Investor call and webcast information
Fourth quarter and full year 2022 financial results
Revenue: Recognised revenue for the three and twelve months ended
Research and development expenses: R&D expenses for the three and twelve months ended
General and administrative expenses: G&A expenses for the three and twelve months ended
Cash inflows: For the full year 2022,
Net Operating cash flow and cash balance: For the full year ending
-
Includes constant currency mark-to-market foreign exchange impact of negative
12% based on the strength of the USD during the year -
During the year,
Exscientia recognised net foreign exchange gains of$27.0 million - The Company holds its deposits in both GBP and USD intended to match expected operational cash needs in order to limit the impact of exchange rate fluctuations
SELECTED CONSOLIDATED STATEMENT OF OPERATIONS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
Three months ended
|
Twelve months ended
|
||
|
2022 |
2021 |
2022 |
2021 |
Revenue |
8.2 |
5.0 |
32.9 |
33.0 |
Cost of sales |
(11.5) |
(5.8) |
(40.2) |
(20.7) |
Research and development expenses |
(43.0) |
(22.6) |
(155.6) |
(53.2) |
General and administrative expenses |
(9.9) |
(7.7) |
(46.4) |
(31.1) |
Operating expenses |
(64.4) |
(36.1) |
(242.2) |
(105.0) |
Foreign exchange gains/(losses) |
(7.6) |
2.6 |
40.6 |
1.1 |
Loss on forward contracts |
- |
- |
(13.6) |
- |
Other income |
1.9 |
0.9 |
6.9 |
4.5 |
Operating loss |
(61.9) |
(27.6) |
(175.4) |
(66.4) |
Finance income/(expense) |
3.5 |
- |
6.5 |
(0.1) |
Share of loss on joint ventures |
- |
(0.2) |
(0.8) |
(1.4) |
Loss before taxation |
(58.4) |
(27.8) |
(169.7) |
(67.9) |
Income tax benefit |
11.3 |
3.6 |
26.5 |
8.4 |
Loss for the period |
(47.2) |
(24.2) |
(143.4) |
(59.5) |
Net loss per share |
(0.38) |
(0.22) |
(1.17) |
(1.20) |
SELECTED CONSOLIDATED BALANCE SHEET, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
|
|
Cash, cash equivalents and short term bank deposits |
610.9 |
678.9 |
Total assets |
784.6 |
773.7 |
Total equity |
578.3 |
684.5 |
Total liabilities |
206.3 |
89.2 |
Total equity and liabilities |
784.6 |
773.7 |
SELECTED CONSOLIDATED STATEMENT OF CASH FLOWS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
Twelve months ended |
|
|
2022 |
2021 |
Net cash outflows from operating activities |
(73.1) |
(8.1) |
Net cash flows used in investing activities |
(148.2) |
(32.1) |
Net cash (used in)/generated from financing activities |
(4.8) |
643.6 |
Net (decrease)/increase in cash and cash equivalents |
(226.1) |
603.4 |
Exchange gain/(loss) on cash and cash equivalents |
35.7 |
(0.1) |
Net (decrease)/increase in cash, cash equivalents and short-term bank deposits* |
(68.1) |
603.3 |
*includes both increases in short term bank deposits and foreign exchange gains/(losses) on cash and cash equivalents
About
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Forward-looking statements
This press release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995, including with respect to the progress of discovery and development of candidate molecules, and the timing and progress of, and data reported from, clinical trials of Exscientia’s product candidates. Any statement describing Exscientia’s goals, plans, expectations, projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to a number of risks, uncertainties and assumptions, including those related to: the initiation, scope and progress of Exscientia’s and its partners’ planned and ongoing pre-clinical studies and clinical trials and ramifications for the cost thereof; clinical, scientific, regulatory and technical developments; the process of discovering, developing and commercialising product candidates that are safe and effective for use as human therapeutics; and the endeavour of building a business around such product candidates. In light of these risks and uncertainties, and other risks and uncertainties that are described in the Risk Factors section and other sections of Exscientia’s Annual Report on Form 20-F, filed with the
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FAQ
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