Exscientia Business Update for First Quarter 2022
Exscientia plc (NASDAQ: EXAI) reported a successful first quarter of 2022, achieving $9.2 million in revenue, up from $7.0 million in Q1 2021. The company has advanced its collaborations, notably with Sanofi and Bristol Myers Squibb, enhancing its AI-driven precision medicine capabilities. Exscientia ended the quarter with $719.8 million in cash, despite operational cash outflows of $10.4 million. Noteworthy progress includes the launch of Xcellomics™ and presentations at the AACR Annual Meeting, underscoring its leadership in AI-designed drug development.
- Revenue increased to $9.2 million in Q1 2022, up from $7.0 million in Q1 2021.
- $6.4 million cash inflows from collaborations in Q1 2022, significantly higher than $0.2 million in Q1 2021.
- Strong cash position with $719.8 million in cash and cash equivalents as of March 31, 2022.
- Successful collaboration with Sanofi, including a $100 million upfront payment received in April 2022.
- Significant advancements presented at the AACR Annual Meeting in AI-driven drug design and precision medicine.
- Operational cash outflows of approximately $10.4 million in Q1 2022.
- Increased general and administrative expenses rising to $10.3 million, a $6.0 million increase from Q1 2021.
- Net loss for the period was $20.4 million, compared to a loss of $7.2 million in the same period of 2021.
Recent advancements in the Company’s pipeline, collaborations, and operations, as well as financial results for the first quarter 2022, are summarised below. In addition,
"We started 2022 by commencing a groundbreaking collaboration with Sanofi to develop a pipeline of AI-designed medicines utilising the breadth of our end-to-end platform of AI-driven capabilities from target prioritisation, to drug engineering and patient selection. At this year's
Recent Highlights
Recent progress demonstrates the Company’s patient tissue-derived translational capabilities, including identifying novel targets, evaluating modulation of complex tumour microenvironments, and enabling patient selection through biomarkers
-
-
Enriching for adenosine antagonist patient responses through deep learning: in this study, researchers modelled and functionally evaluated patient gene signatures to map the association of anti-cancer immune activity with the inhibition of adenosine signalling by EXS-21546,
Exscientia's clinical stage A2a antagonist. These data suggest stratification of gene signatures could be used in future clinical studies to identify patients that may best respond to A2aR targeted therapies. - AI-driven discovery and profiling of GTAEXS-617, a selective and highly potent inhibitor of CDK7: preclinical data highlighting potential benefits of Exscientia’s AI-driven design to overcome identified issues with CDK7 inhibitors, including toxicity and selectivity. In addition, the precision medicine platform identified patient subsegments that can inform biomarker strategies.
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Deep learning supported high content analysis of primary patient samples identifies ALK inhibition as a novel mechanism of action in a subset of ovarian cancers: research highlighting the potential of
Exscientia's precision medicine platform to identify novel targets and targetable pathways using human disease-relevant patient tissue models, which could have the potential to improve patient outcomes by uncovering clinical relevance at the target discovery stage.
- Together with the
Continued to identify and validate new targets, as well as progress and prioritise broad pipeline
- Partnered programmes
-
Extended collaboration with Bristol Myers Squibb (BMS) to generate additional data including the use of precision medicine capabilities for key targets under the collaboration;
in cash inflows in first quarter 2022 to be recognised as revenue throughout 2022$5 million -
Target identification and validation ongoing in Sanofi collaboration, signed in
January 2022 , leveraging precision medicine platform and Centaur Biologist
- Co-owned programmes
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GTAEXS-617 CTA submission expected by year-end 2022, progress in generating data in additional tumour types to inform planned Phase I clinical trial in cancer patients
- CTA and IND-enabling studies are ongoing, including pre-clinical studies to explore potential dosing regimens for planned clinical trials
- Wholly and majority owned programmes
-
EXS-21546 top-line data for Phase 1 healthy volunteer study on track for the first half of 2022
- Anticipate commencing Phase 1b/2 study in patients with high adenosine signature cancers in the second half of 2022
Strong balance sheet and anticipated cash flows position Company for execution
-
- First quarter 2022 net cash outflows from operations of approximately
-
Further expanded Exscientia’s leadership team
-
Investor Call and Webcast Information
First Quarter 2022 Financial Results
For the convenience of the reader, the Company has translated pound sterling amounts to
Revenue: Revenue for the first quarter 2022, was
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
|
Total |
||||
Partnered Programmes |
7.4 |
- |
- |
7.4 |
||||
Co-owned Programmes |
- |
3.7 |
0.4 |
4.1 |
||||
Internal Pipeline and |
- |
27.1 |
- |
27.1 |
||||
Total |
7.4 |
30.8 |
0.4 |
38.6 |
General and administrative expenses: G&A expenses for the three months ended
Cash inflows: For the first quarter 2022,
Cash and cash equivalents: Cash and cash equivalents as of
SELECTED CONSOLIDATED STATEMENT OF OPERATIONS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
Three months ended |
|
|
2022 |
2021 |
Revenue |
9.2 |
7.0 |
Cost of sales |
(7.4) |
(5.1) |
Research and development expenses |
(30.8) |
(5.6) |
General and administrative expenses |
(10.3) |
(4.3) |
Operating expenses |
(48.5) |
(15.0) |
Foreign exchange gains/(losses) |
12.7 |
(0.2) |
Other income |
1.9 |
0.6 |
Operating loss |
(24.7) |
(7.6) |
Finance income/(expense) |
(0.0) |
(0.0) |
Share of loss on joint ventures |
(0.4) |
(0.5) |
Loss before taxation |
(25.1) |
(8.1) |
Income tax benefit |
4.7 |
0.9 |
Loss for the period |
(20.4) |
(7.2) |
Net loss per share |
(0.41) |
(0.23) |
SELECTED CONSOLIDATED BALANCE SHEET, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
|
|
||||
Cash and cash equivalents |
719.8 |
739.4 |
||||
Total assets |
944.9 |
842.6 |
||||
Total equity |
727.4 |
745.5 |
||||
Total liabilities |
217.5 |
97.1 |
||||
Total equity and liabilities |
944.9 |
842.6 |
SELECTED CONSOLIDATED STATEMENT OF CASH FLOWS. CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
|
|
||||
Net cash flows used in operating activities |
(10.4) |
(11.8) |
||||
Net cash flows used in investing activities |
(5.7) |
(2.6) |
||||
Net cash generated from financing activities |
(3.5) |
27.5 |
||||
Net increase in cash and cash equivalents |
(19.6) |
13.1 |
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, 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, and 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; and those inherent in the process of discovering, developing and commercialising product candidates that are safe and effective for use as human therapeutics, and in 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 Registration Statement on Form 20-F, filed with the
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