Exscientia Business Update for Second Quarter and First Half 2022
Exscientia plc (Nasdaq: EXAI) reported significant advancements in its drug discovery pipeline during Q2 2022, including positive topline data from its EXS-21546 program. The company ended the first half of 2022 with $732 million in cash, having generated $111 million in cash inflows from collaborations, notably $100 million from Sanofi. However, the company recognized an operating loss of $41.2 million and a net loss of $34.8 million for the quarter. With heightened R&D costs of $40.2 million, Exscientia aims to leverage its precision medicine platform for future growth.
- Generated $111 million in cash inflows from collaborations in Q2 2022.
- Ended H1 2022 with $732 million in cash, cash equivalents, and short-term bank deposits.
- Announced positive topline data from EXS-21546, indicating sustained target engagement.
- First precision medicine project initiated with Sanofi, enhancing pipeline diversity.
- Reported an operating loss of $41.2 million for Q2 2022.
- Net loss increased to $34.8 million, compared to the previous year.
- R&D expenses surged to $40.2 million, raising concerns over cost management.
Recent developments in the Company’s pipeline, collaborations, and operations, as well as financial results for the second quarter and first half 2022, are summarised below. In addition,
“In the first half of 2022, we delivered on major new and existing collaborations, advanced our pipeline programmes, and marked the 10-year anniversary of Exscientia’s founding. Over the past decade, we’ve pioneered an AI-driven approach to modernising drug discovery and development, and it was fitting that this quarter we also announced topline data from our EXS-21546 programme, one of the first AI-designed molecules to enter clinical trials,” said
Recent Highlights
Progress across internal and partnered pipeline, leveraging the Company's precision medicine platform, as well as key components of
Internal pipeline
Wholly, majority and co-owned programmes focused on areas in which
-
Following topline data in June, the Company remains on track to initiate a Phase 1b/2 study of EXS-21546 (majority owned with Evotec) in the second half of 2022
-
Phase 1b/2 study will be optimised with simulation-guided clinical trial design principles as well as leverage
Exscientia's precision medicine platform to maximise potential impact to the most relevant patients
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Phase 1b/2 study will be optimised with simulation-guided clinical trial design principles as well as leverage
-
GTAEXS-617 (co-owned with GT Apeiron) CTA submission expected by year-end 2022
- CTA and IND-enabling studies are ongoing, including translational work to support planned clinical trials expected to start in the first half of 2023
Partnered programmes
Utilising a scalable end-to-end platform to advance a broad pipeline, while also generating significant cash inflows to support advancements
- First two targets identified in new Sanofi collaboration for oncology and inflammation & immunity, respectively
- First precision medicine project initiated; focused on patient enrichment for a Sanofi biologic in oncology
- Advancing Bristol Myers Squibb (BMS) collaboration with continued progress across both BMS1 and BMS2 collaborations
-
Following the achievement of recent successful drug discovery milestone,
Exscientia and Bayer have mutually agreed to end collaboration;Exscientia will retain optionality to develop one of the two targets pursued under the collaboration-
The Bayer agreement was the last
Exscientia partnership based on AI-only design services, which included lower economics and reduced operational involvement in comparison with more recent partnerships - This update aligns with Company strategy to increasingly focus on programmes where Exscientia’s AI design, experimental biology and precision medicine platforms can be integrated
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The Bayer agreement was the last
Recent clinical progress highlights ability of the Company’s advanced, AI-based platform to create novel molecules with high level of translatability to human biology
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Announced topline data from EXS-21546 Phase 1a healthy volunteer study in
June 2022 - The study demonstrated that observed human pharmacokinetics for EXS-21546 were in line with what had been designed for and predicted in preclinical modelling, supporting a twice-daily (BID) dose for continuous A2A receptor inhibition over a dosing interval
- EXS-21546 signalled inhibition of A2A receptor was sustained over the BID dosing period, demonstrating a level of lasting target engagement
- EXS-21546 was well-tolerated with no CNS adverse events reported in the SAD portion at all doses (30mg, 90mg, 250mg, 400mg) and in the MAD portion at 150mg BID
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cash flow from collaborations in second quarter 2022, including$111.0 million from Sanofi, ending the first half 2022 with$100.0 million in cash, cash equivalents and short-term bank deposits$732.0 million -
Includes constant currency mark-to-market foreign exchange impact of negative
8% -
During the quarter,
Exscientia recognised realised foreign exchange gains net of forward contract settlements of . The Company holds its deposits in both GBP and USD intended to match expected cash needs while limiting the impact of exchange rate fluctuations$14.0 million
-
Includes constant currency mark-to-market foreign exchange impact of negative
-
Second quarter 2022 net positive cash inflows from operations of
$72.9 million
Expanded leadership team in critical growth areas
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Eileen Jennings-Brown joined asExscientia's Chief Information Officer, reporting toGarry Pairaudeau , Chief Technology Officer, and responsible for overseeing IT and DevOps. Ms. Jennings-Brown brings more than 25 years of experience across IT roles, including most recently heading technology for theWellcome Trust . -
Charlotte Deane , Ph.D., Chief Scientist of Biologics AI, who joinedExscientia inJanuary 2022 , was awarded an appointment to the Most Excellent Order of the British Empire (MBE) for leading theUK Research and Innovation's rapid response call for projects addressing issues arising from the pandemic.
Select peer-reviewed publications and scientific meeting presentations during the quarter
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“Coverage Score: A Model Agnostic Method to Efficiently Explore Chemical Space,” was published in the
Journal of Chemical Information and Modeling inJuly 2022 . This advancement in active learning allows more efficient exploration of chemical space, potentially leading to increased diversity of candidates, faster model improvement and shorter time to candidate identification -
“Surface Plasmon Resonance Screening to Identify Active and Selective Adenosine Receptor Binding Fragments,” a study which further validates
Exscientia's innovative biosensor approach to screening wildtype GPCR targets to advance drug discovery, was published in the ACS Medicinal Chemistry Letters inJune 2022 - Three posters presented at the AACR Annual Meeting in April, highlighting Exscientia’s human tissue precision medicine platform, including potential benefits of Exscientia’s AI-driven design to overcome known issues such as potency, toxicity and selectivity and improve patient outcomes
Investor call and webcast information
Second quarter and first half 2022 financial results
For the convenience of the reader, the Company has translated pound sterling amounts to
Revenue: Recognised revenue for the three and six months ended
R&D and cost of drug discovery: Due to various collaboration structures, expenditure incurred in relation to research and development activities may be recognised within one of several financial statement captions. The tables below show how these expenses are separated across the accounting categories.
Three months ended
|
COGS |
R&D |
Share of JV
|
Total |
Partnered Programmes |
10.9 |
– |
– |
10.9 |
Internal Pipeline and Technology Development |
– |
40.2 |
0.3 |
40.5 |
Total |
10.9 |
40.2 |
0.3 |
51.4 |
Six months ended
|
COGS |
R&D |
Share of JV
|
Total |
Partnered Programmes |
17.7 |
– |
– |
17.7 |
Internal Pipeline and Technology Development |
– |
68.8 |
0.7 |
69.5 |
Total |
17.7 |
68.8 |
0.7 |
87.2 |
Research and development expenses: R&D expenses for the three and six months ended
General and administrative expenses: G&A expenses for the three and six months ended
Cash inflows: For the second quarter 2022,
Cash, cash equivalents and bank deposits: Cash, cash equivalents and bank deposits as of
SELECTED CONSOLIDATED STATEMENT OF OPERATIONS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
Three months ended
|
Six months ended
|
||
|
2022 |
2021 |
2022 |
2021 |
Revenue |
8.7 |
0.4 |
17.2 |
6.8 |
Cost of sales |
(10.9) |
(4.4) |
(17.7) |
(9.1) |
Research and development expenses |
(40.2) |
(10.0) |
(68.8) |
(15.1) |
General and administrative expenses |
(14.7) |
(9.1) |
(24.2) |
(13.1) |
Operating expenses |
(65.8) |
(23.5) |
(110.7) |
(37.3) |
Foreign exchange gains/(losses) |
27.7 |
(3.4) |
39.5 |
(3.5) |
Loss on forward contracts |
(13.7) |
- |
(13.7) |
- |
Other income |
1.9 |
1.0 |
3.6 |
1.5 |
Operating loss |
(41.2) |
(25.5) |
(64.1) |
(32.5) |
Finance income/(expense) |
0.4 |
- |
0.5 |
(0.1) |
Share of loss on joint ventures |
(0.3) |
(0.5) |
(0.7) |
(0.9) |
Gain on derivative financial instrument |
0.0 |
1.7 |
- |
1.7 |
Loss before taxation |
(41.1) |
(24.3) |
(64.3) |
(31.8) |
Income tax benefit |
6.3 |
1.7 |
10.6 |
2.6 |
Loss for the period |
(34.8) |
(22.6) |
(53.7) |
(29.2) |
Net loss per share |
(0.29) |
(0.86) |
(0.44) |
(1.02) |
SELECTED CONSOLIDATED BALANCE SHEET, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
June 30, 2022 |
December 31, 2021 |
Cash, cash equivalents & short-term bank deposits |
732.0 |
683.7 |
Total assets |
849.0 |
779.2 |
Total equity |
650.8 |
689.4 |
Total liabilities |
198.2 |
89.8 |
Total equity and liabilities |
849.0 |
779.2 |
SELECTED CONSOLIDATED STATEMENT OF CASH FLOWS. CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
June 30, 2022 |
June 30, 2021 |
Net cash flows from operating activities |
63.3 |
4.5 |
Net cash flows used in investing activities |
(133.1) |
(4.2) |
Net cash flows from financing activities |
(3.7) |
222.3 |
Net (decrease)/increase in cash and cash equivalents |
(73.5) |
222.6 |
Net increase in cash, cash equivalents and short-term bank deposits |
48.2 |
222.6 |
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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, and Exscientia’s expectations regarding its projected revenue and cash runway. Any statement describing Exscientia’s goals, plans, expectations, financial or other 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 impact that the COVID-19 pandemic could have on the Company’s business, including the scope, progress and expansion of Exscientia’s product development efforts; 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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