Exscientia Business Update for First Quarter 2024
Exscientia (Nasdaq: EXAI) released its Q1 2024 business update. The company reported positive early Phase 1 results for its BMS-partnered EXS4318 (PKC-theta inhibitor) program. Initial Phase I data for GTAEXS617 (CDK7 inhibitor) and EXS74539 (LSD1 inhibitor) are expected in 2H24. Exscientia's AI-driven automation lab aims to streamline drug design processes, targeting $40M in annual savings by 2025. The company plans to reduce headcount by 20-25% by year-end, expecting savings despite incurring $7.4M-$9.6M in severance costs. Financially, Q1 revenue was $6.7M, down from $7.3M YoY, while R&D expenses dropped to $29.8M from $42.2M. Exscientia projects its cash reserves will fund operations into 2027. The company will host a conference call on May 21 to discuss these updates.
- Positive early Phase 1 results for EXS4318 (PKC-theta inhibitor).
- Advancements in EXS74539 (LSD1 inhibitor) and EXS73565 (MALT1 inhibitor) expected in 2H24 and early 2025.
- Automation lab initiated three drug discovery programs, expected to be fully operational by year-end.
- Company targets $40M annual savings by 2025 through operational efficiencies.
- Q1 R&D expenses decreased to $29.8M from $42.2M, reflecting cost reductions and operational efficiencies.
- Cash inflows from collaborations increased to $4.5M from $0.5M YoY.
- Net operating cash outflows reduced to $39.0M from $54.8M YoY.
- Q1 2024 revenue declined to $6.7M from $7.3M YoY.
- Operating expenses decreased to $43.5M from $66.7M but remain high.
- Net loss for Q1 2024 was $26.5M, compared to $47.5M YoY.
- Cash balance fell to $416.9M from $458.8M at the end of 2023.
- Headcount reduction by 20-25% expected to incur $7.4M-$9.6M in severance costs.
- Net decrease in cash and cash equivalents was $103.1M in Q1 2024.
Insights
Looking at the financial results for the first quarter of 2024, a mixed picture emerges. Revenue decreased to
On the brighter side, R&D expenses saw a significant cut from
Notably, G&A expenses reduced sharply from
Overall, the company's net loss improved from
For retail investors, the financials suggest Exscientia is tightening its belt, focusing on operational efficiency and sustaining its cash flow. These measures may be favorable in the long run, but immediate cautiousness is warranted given the mixed revenue picture and the potential risks of aggressive cost-cutting in R&D.
Exscientia's advanced clinical pipeline demonstrates significant progress and the potential for impactful breakthroughs, particularly in oncology and immunology. The Phase 1 success of the PKC-theta inhibitor, EXS4318, partnered with Bristol Myers Squibb, could position the company as a frontrunner in the immunology segment. This is noteworthy, especially given the drug's potential first-in-class status, designed after traditional approaches failed to yield results.
The ongoing Phase 1/2 ELUCIDATE trial for '617 (CDK7 inhibitor) is another key aspect to watch. It aims to treat advanced solid tumors, with the company moving into a combination phase in the second half of 2024. This trial's success could elevate the company's profile in oncological therapies, offering alternative treatments where current options are limited.
Additionally, the LSD1 inhibitor '539 and MALT1 inhibitor '565 are progressing towards clinical trials, targeting acute myeloid leukemia and B-cell malignancies, respectively. These internal projects underline Exscientia's focus on developing novel treatments based on AI-driven drug design.
For investors, the clinical progress is promising, with several candidates showing potential to advance the company's reputation and market position. However, clinical trials are inherently high-risk and investors should keep an eye on future trial results and regulatory milestones.
Exscientia's integration of AI in drug discovery, coupled with its fully automated experimentation platform, stands out as a game-changer in the industry. The company's automation laboratory promises to revolutionize the drug development process by significantly reducing time and costs. The fully automated, generative design-make-test-learn (DMTL) loops enable rapid cycles of drug design and testing without human intervention.
This approach not only enhances the speed and quality of drug discovery but also minimizes the reliance on contract research organizations, thereby cutting down outsourcing costs. The ability to streamline operations while maintaining a robust pipeline is a compelling narrative for the company's future prospects.
For retail investors, the key takeaway is that Exscientia's technological advancements could redefine how drugs are discovered and developed, potentially making it a leader in a highly competitive market. The emphasis on AI and automation aligns with industry trends towards increased efficiency and precision in drug development. However, it's essential to monitor how these technological innovations translate into tangible clinical and financial outcomes.
Positive early Phase 1 results for BMS-partnered programme ‘4318 (PKC-theta inhibitor)
GTAEXS617 (CDK7 inhibitor) initial Phase I data expected in 2H24
LSD1 and MALT1 inhibitor programmes expected to advance into clinic in 2H24 and early 2025, respectively
AI-design integration enhanced with full experiment automation driving towards maximum speed, quality and autonomous drug design
Leveraging technology advancements and streamlining operations to realise annualised savings of
“With the ramp up of activities at our automation lab, we are beginning to see the transformative power of fully integrating AI drug design with the sheer capacity of comprehensive robotic automation across the entire experimentation cycle,” said Dr. David Hallett, interim Chief Executive Officer and Chief Scientific Officer of Exscientia. “In addition, this year, we are excited about the potential for both GTAEXS617 (or ‘617) and EXS4318 (or ‘4318) to show superior clinical profiles over complex candidate therapies created through traditional methods. We will continue expanding our oncology-focused internal clinical stage pipeline and anticipate advancing both our LSD1 and MALT1 inhibitor programmes forward. The investments into our platform which we have made over the years are bearing fruit. This, in combination with ever-increasing focus on efficiency, allows us to further streamline our operations while delivering on our mid-term goals.”
Key Business Updates
Pipeline
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Patient enrolment for the dose escalation phase of the Company’s adaptive Phase 1/2 ELUCIDATE trial evaluating ‘617, a potential best-in-class CDK7 inhibitor for the treatment of advanced solid tumours, is ongoing. Exscientia anticipates moving into a combination phase of the trial in the second half of 2024
- The Company expects to announce topline pharmacokinetics and safety data from the dose escalation phase of the trial in the second half of 2024
- EXS74539 (‘539), Exscientia’s highly differentiated LSD1 inhibitor, is advancing through IND/CTA-enabling studies. The Company anticipates submitting an IND or CTA in the third quarter of 2024, with the goal to initiate a Phase 1/2 clinical trial in AML patients by the end of 2024
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Based on patient unmet need, supporting preclinical data and the unique precision designed properties of Exscientia’s MALT1 inhibitor, EXS73565 (‘565), the Company is preparing to submit an IND or CTA in the second half of 2024 to study ‘565 in a Phase 1/2 clinical trial in B-cell malignancies, including CLL, which Exscientia expects to launch in early 2025
- This clinical development programme aims to support the assessment of ‘565 in combination with current standard of care options
Collaborations & Partnerships
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EXS4318 (‘4318), a potential first-in-class PKC-theta inhibitor designed by Exscientia and in-licensed by Bristol Myers Squibb, has shown positive early results in its Phase 1 study and has the potential to be a first-in-class immunology drug
- Exscientia designed the first potent and selective PKC-theta inhibitor after over ten biopharma companies halted programmes for drug candidates designed using traditional drug discovery techniques
- Exscientia retains rights to receive milestone payments and potential royalties for ‘4318
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The Sanofi partnership continues to make strong progress across multiple programmes, primarily focused on inflammation & immunology targets
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Exscientia received a
$4.0 million
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Exscientia received a
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Exscientia’s collaboration with Merck KGaA, Darmstadt,
Germany continues to advance with multiple programmes now in early discovery
Advancing autonomous drug design and experimentation
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The first three drug discovery programmes have been initiated in the Company’s novel, industry leading discovery automation laboratory
- The facility is expected to be fully operational by year end - additional drug discovery programmes are expected to commence on the platform in the coming months
- The automation lab tightly integrates artificial intelligence with robotic experimentation creating fully automated, generative design-make-test-learn (DMTL) loops
- This has the potential to dramatically reduce the time and cost of discovery cycles and lower the need for contract research organisations as well as redefining how AI-based design can be autonomously integrated with laboratory experimentation
Benefits from integration of technology and streamlining activities continues to improve operational efficiencies
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While continuing to focus on its strategic priorities, Exscientia will initiate efficiency measures through the rest of the year designed to streamline the Company’s operations, which it expects to result in annualised savings of
$40 million - A number of Exscientia’s multi-year investments, including projects related to its proprietary technology platform, are coming to conclusion and expected to result in efficiency gains
- The changes also leverage the expected efficiency gains from the Company’s automation laboratory and will not impact the internal pipeline, partnership or drug design activities
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As part of these cost efficiency measures, a 20
-25% headcount reduction is expected to be completed by the end of 2024, targeting some areas of target identification, precision medicine, experimentation, engineering and infrastructure -
The initiative is expected to result in severance and termination-related costs that will be between approximately
$7.4 million $9.6 million - Excluding any potential cash inflows from new business development or financing, these changes are expected to extend the Company’s cash runway well into 2027
Investor Call and Webcast Information
Exscientia will host a conference call on Tuesday, May 21st at 1:30 p.m. BST / 8:30 a.m. EDT. A webcast of the live call can be accessed by visiting the “Investors and Media” section of the Company’s website at investors.exscientia.ai. Alternatively, the live conference call can be accessed by dialling +1 (888) 330 3292 (
First Quarter 2024 Financial Results
For the convenience of the reader, the Company has translated pound sterling amounts to
Revenue: Revenue for the first quarter of 2024 was
Research and development expenses (R&D): R&D expenses for the three months ended March 31, 2024 were
General and administrative expenses (G&A): G&A expenses for the three months ended March 31, 2024 were
Cash inflows: For the three months ended March 31, 2024, Exscientia received
Net operating cash flow and cash balance: For the three months ended March 31, 2024, net operating cash outflows were
Based on its current operating plans, including the addition of the Sanofi programme and after accounting for the headcount reduction and other anticipated cost efficiencies, the Company believes that its existing cash, cash equivalents and short-term bank deposits and anticipated milestones will be sufficient to fund its operations and capital expenditure requirements well into 2027. This estimate excludes any potential cash inflows from new business development or financing activities.
SELECTED CONSOLIDATED STATEMENT OF OPERATIONS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
Three months ended March 31, |
|||
|
2024 |
2023 |
||
Revenue |
6.7 |
7.3 |
||
Cost of sales |
(9.4) |
(10.7) |
||
Research and development expenses |
(29.8) |
(42.2) |
||
General and administrative expenses |
(4.3) |
(13.8) |
||
Operating expenses |
(43.5) |
(66.7) |
||
Foreign exchange gains/(losses) |
1.1 |
(1.5) |
||
Other income |
1.6 |
3.3 |
||
Operating loss |
(34.1) |
(57.6) |
||
Net finance income |
4.6 |
4.2 |
||
Share of loss on joint ventures |
(0.7) |
(0.6) |
||
Loss before taxation |
(30.2) |
(54.0) |
||
Income tax benefit |
3.7 |
6.5 |
||
Loss for the period |
(26.5) |
(47.5) |
||
Net loss per share |
(0.21) |
(0.39) |
||
Weighted average shares outstanding (basic and diluted) |
125,975,607 |
123,257,529 |
||
SELECTED CONSOLIDATED BALANCE SHEET, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
March 31, 2024 |
December 31, 2023 |
||
Cash, cash equivalents and short term deposits |
416.9 |
458.8 |
||
Total assets |
598.4 |
645.4 |
||
Total equity |
417.7 |
449.5 |
||
Total liabilities |
180.7 |
195.9 |
||
Total equity and liabilities |
598.4 |
645.4 |
SELECTED CONSOLIDATED STATEMENT OF CASH FLOWS, CONSTANT CURRENCY CONVERSION (unaudited)
($ millions, except per share data, at the rate of
|
March 31, 2024 |
March 31, 2023 |
||
Net cash outflows from operating activities |
(39.0) |
(54.8) |
||
Net cash flows used in investing activities |
(63.0) |
(206.5) |
||
Net cash used in financing activities |
(1.1) |
(0.9) |
||
Net decrease in cash and cash equivalents |
(103.1) |
(262.2) |
||
Exchange gain/(loss) on cash and cash equivalents |
0.6 |
(2.1) |
||
Net decrease in cash, cash equivalents and short-term bank deposits* |
(41.9) |
(73.9) |
||
* Includes both increases in short term bank deposits and foreign exchange gains/(losses) on cash and cash equivalents
About Exscientia
Exscientia is an AI-driven precision medicine company committed to discovering, designing, and developing the best possible drugs in the fastest and most effective manner. Exscientia developed the first-ever functional precision oncology platform to successfully guide treatment selection and improve patient outcomes in a prospective interventional clinical study, as well as to progress AI-designed small molecules into the clinical setting. Our internal pipeline is focused on leveraging our precision medicine platform in oncology, while our partnered pipeline broadens our approach to other therapeutic areas. By pioneering a new approach to medicine creation, we believe the best ideas of science can rapidly become the best medicines for patients.
For more information visit us on www.exscientia.ai or follow us on LinkedIn @ex-scientia and X @exscientiaAI.
Forward-Looking Statements
This press release contains certain forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Words such as “anticipates,” “believes,” “expects,” “intends,” and “projects” or similar expressions are intended to identify forward-looking statements. These forward-looking statements, include statements with regard to Exscientia’s expectations regarding: the initiation, timing and progress of, and data collected during and reported from, the Company’s and its partners’ clinical trials, as well as expectations with respect to the outcome or benefit of such trials; the progress of Exscientia’s collaborations and partnered programmes; the commencement of additional discovery programmes using Exscientia’s platform and automation facility; the timing and outcome of and any anticipated savings from Exscientia’s planned headcount reduction and other cost efficiency measures; and the Company’s expectation that its existing cash, cash equivalents and short-term bank deposits will be sufficient to fund its operations well into 2027. 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 preclinical studies and clinical trials and ramifications for the cost thereof; clinical, scientific, regulatory and technical developments; the development and deployment of new technology and facilities; the timing and effects of the planned headcount reduction and other cost efficiency measures; and 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 Securities and Exchange Commission (SEC) on March 21, 2024, and other filings that Exscientia makes with the SEC from time to time (which are available at https://www.sec.gov/), the events and circumstances discussed in such forward-looking statements may not occur, and Exscientia’s actual results could differ materially and adversely from those anticipated or implied thereby. Although Exscientia’s forward-looking statements reflect the good faith judgement of its management, these statements are based only on facts and factors currently known by the Company. As a result, investors are cautioned not to rely on these forward-looking statements. Exscientia undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required by law.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240521942319/en/
Investor Relations:
Sara Sherman / Chinedu Okeke
investors@exscientia.ai
Media:
Oliver Stohlmann
media@exscientia.ai
Source: Exscientia plc
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