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Relay Therapeutics Reports First Quarter 2024 Financial Results and Corporate Highlights

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Relay Therapeutics, Inc. reported first quarter 2024 financial results with $750 million in cash, cash equivalents, and investments, funding operations into the second half of 2026. The company highlighted progress in RLY-2608 development program, enrollment in RLY-2608 doublet and triplet studies, and anticipation of data updates for RLY-2608 and Lirafugratinib in the second half of 2024. Financially, revenue increased to $10.0 million, R&D expenses decreased, G&A expenses increased slightly, and net loss improved compared to the first quarter of 2023.

Positive
  • Strong cash position of $750 million to fund operations into the second half of 2026.

  • Revenue increased to $10.0 million in the first quarter of 2024.

  • Progress in RLY-2608 development program and enrollment in doublet and triplet studies.

  • Anticipation of data updates for RLY-2608 and Lirafugratinib in the second half of 2024.

Negative
  • Research and development expenses were $82.4 million in the first quarter of 2024.

  • Net loss was $81.4 million for the first quarter of 2024.

  • General and administrative expenses increased slightly to $19.8 million in the first quarter of 2024.

Insights

Relay Therapeutics' financial strength is evidenced by its substantial cash reserves, totaling $749.6 million, which is indicative of a well-capitalized company with a runway into the second half of 2026. The minor decrease from the last quarter reflects prudent cash burn rate management. The significant increase in revenue to $10.0 million, stemming from a milestone payment from Genentech, highlights the value of strategic partnerships and the potential for non-dilutive funding. However, investors should note the net loss of $81.4 million, although improved from the previous year's $94.2 million. This improvement in net loss, coupled with a slight reduction in R&D expenses, suggests a degree of financial discipline.

The ongoing RLY-2608 development program and upcoming data releases could serve as significant value inflection points for Relay Therapeutics, given the focus on PI3Kα-mutant, HR+, HER2- locally advanced or metastatic breast cancer, a subtype with a clear unmet need. The combination therapy approach, including the planned safety data update for the RLY-2608 + fulvestrant + ribociclib triplet, may showcase the company's strategic direction in precision medicine. However, the decision to minimize resources on Lirafugratinib in order to allow data maturation indicates a more cautious approach, aligning resources to the most promising leads, a common strategy within the biotech industry to maximize R&D efficiency.

The advancement of Relay Therapeutics' pre-clinical pipeline, with a promise to disclose new program(s) in 2024, reflects strategic innovation within the company. The focus on first-in-class potential underscores the company's commitment to pioneering novel therapeutic options. Investors should recognize the inherent risk of pre-clinical development, as many compounds do not advance to clinical stages, but also the high rewards associated with successful novel drug entities, especially in the precision medicine space where targets are carefully selected based on genetic profiles.

Approximately $750 million in cash, cash equivalents and investments at end of Q1 2024, expected to fund operations into second half of 2026

CAMBRIDGE, Mass., May 02, 2024 (GLOBE NEWSWIRE) -- Relay Therapeutics, Inc. (Nasdaq: RLAY), a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies, today reported first quarter 2024 financial results and corporate highlights.

“We have started 2024 with a focus on maintaining strong execution across our portfolio,” said Sanjiv Patel, M.D., President and Chief Executive Officer of Relay Therapeutics. “We continue to progress a robust RLY-2608 development program and expect to share additional data in the second half of the year. In parallel, we have continued to advance our pre-clinical pipeline and look forward to disclosing at least one new program this year, which is being designed to have first-in-class potential.”

Recent Corporate Highlights

RLY-2608 (ReDiscover study)

  • RLY-2608 doublet: continued to enroll patients with PI3Kα-mutant, HR+, HER2- locally advanced or metastatic breast cancer in two additional dose expansion cohorts of RLY-2608 in combination with fulvestrant – a second 600mg BID cohort as well as one at 400mg BID
  • RLY-2608 triplet: continued enrollment of RLY-2608 + fulvestrant + ribociclib triplet combination in patients with PI3Kα-mutant, HR+, HER2- locally advanced or metastatic breast cancer

Lirafugratinib (RLY-4008; ReFocus study)

  • As previously disclosed, the company will minimize resource allocation in 2024 to allow data to mature and inform future clinical development decisions

Anticipated 2024 Milestones

  • RLY-2608
    • RLY-2608 + fulvestrant data update in the second half of 2024
    • RLY-2608 + fulvestrant + ribociclib initial safety data in the second half of 2024
  • Lirafugratinib: tumor agnostic data and regulatory update in the second half of 2024
  • Pre-clinical: disclose new program(s) in 2024

First Quarter 2024 Financial Results

Cash, Cash Equivalents and Investments: As of March 31, 2024, cash, cash equivalents and investments totaled $749.6 million compared to $750.1 million as of December 31, 2023. The company expects its current cash, cash equivalents and investments will be sufficient to fund its current operating plan into the second half of 2026.

Revenue: Revenue was $10.0 million for the first quarter of 2024, as compared to $0.2 million for the first quarter of 2023. The increase was primarily due to a payment of $10.0 million in connection with a milestone achieved under the company’s Collaboration and License Agreement with Genentech, Inc. during the first quarter of 2024.

R&D Expenses: Research and development expenses were $82.4 million for the first quarter of 2024, as compared to $82.8 million for the first quarter of 2023. The decrease was primarily due to the impact of prioritization of certain programs in our pipeline, as previously disclosed in 2023 and earlier in 2024.

G&A Expenses: General and administrative expenses were $19.8 million for the first quarter of 2024, as compared to $19.6 million for the first quarter of 2023. The increase was primarily due to additional stock compensation expense.

Net Loss: Net loss was $81.4 million for the first quarter of 2024, or a net loss per share of $0.62, as compared to a net loss of $94.2 million for the first quarter of 2023, or a net loss per share of $0.78.

About Relay Therapeutics

Relay Therapeutics (Nasdaq: RLAY) is a clinical-stage precision medicine company transforming the drug discovery process by combining leading-edge computational and experimental technologies with the goal of bringing life-changing therapies to patients. As the first of a new breed of biotech created at the intersection of complementary techniques and technologies, Relay Therapeutics aims to push the boundaries of what’s possible in drug discovery. Its Dynamo™ platform integrates an array of leading-edge computational and experimental approaches designed to drug protein targets that have previously been intractable or inadequately addressed. Relay Therapeutics’ initial focus is on enhancing small molecule therapeutic discovery in targeted oncology and genetic disease indications. For more information, please visit www.relaytx.com or follow us on Twitter.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, implied and express statements regarding Relay Therapeutics’ strategy, business plans and focus; the progress and timing of the clinical development of the programs across Relay Therapeutics’ portfolio, including the expected therapeutic benefits of its programs, potential efficacy and tolerability, and the timing and success of interactions with and approval of regulatory authorities; the timing and progress of doublet and triplet combinations for RLY-2608, the timing of clinical updates for RLY-2608, the timing of a clinical data and regulatory update for lirafugratinib, and the timing of disclosure of additional pre-clinical programs; expectations regarding Relay Therapeutics’ pipeline, operating plan, use of capital, expenses and other financial results; and Relay Therapeutics’ cash runway projection. The words “may,” “might,” “will,” “could,” “would,” “should,” “plan,” “anticipate,” “intend,” “believe,” “expect,” “estimate,” “seek,” “predict,” “future,” “project,” “potential,” “continue,” “target” and similar words or expressions, or the negative thereof, are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words.

Any forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks associated with: the impact of global economic uncertainty, geopolitical instability and conflicts, or public health epidemics or outbreaks of an infectious disease on countries or regions in which Relay Therapeutics has operations or does business, as well as on the timing and anticipated results of its clinical trials, strategy, future operations and profitability; the delay or pause of any current or planned clinical trials or the development of Relay Therapeutics’ drug candidates; the risk that the preliminary results of its pre-clinical or clinical trials may not be predictive of future or final results in connection with future clinical trials of its product candidates; Relay Therapeutics’ ability to successfully demonstrate the safety and efficacy of its drug candidates; the timing and outcome of its planned interactions with regulatory authorities; and obtaining, maintaining and protecting its intellectual property. These and other risks and uncertainties are described in greater detail in the section entitled “Risk Factors” in Relay Therapeutics’ most recent Annual Report on Form 10-K, as well as any subsequent filings with the Securities and Exchange Commission. In addition, any forward-looking statements represent Relay Therapeutics' views only as of today and should not be relied upon as representing its views as of any subsequent date. Relay Therapeutics explicitly disclaims any obligation to update any forward-looking statements. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

Contact:
Megan Goulart
617-545-5526
mgoulart@relaytx.com

Media:
Dan Budwick
1AB
973-271-6085
dan@1abmedia.com

Relay Therapeutics, Inc.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
(Unaudited)
 
  Three Months Ended March 31, 
  2024  2023 
Revenue:      
License and other revenue $10,007  $226 
Total revenue  10,007   226 
Operating expenses:      
Research and development expenses $82,403  $82,827 
Change in fair value of contingent consideration liability  (1,832)  (1,003)
General and administrative expenses  19,799   19,579 
Total operating expenses  100,370   101,403 
Loss from operations  (90,363)  (101,177)
Other income:      
Interest income  8,951   6,941 
Other income (expense)  25   (3)
Total other income, net  8,976   6,938 
Net loss $(81,387) $(94,239)
Net loss per share, basic and diluted $(0.62) $(0.78)
Weighted average shares of common stock, basic and diluted  130,843,013   121,320,865 
Other comprehensive (loss) income:      
Unrealized holding (loss) gain  (962)  4,618 
Total other comprehensive (loss) income  (962)  4,618 
Total comprehensive loss $(82,349) $(89,621)
         


Relay Therapeutics, Inc.
Selected Condensed Consolidated Balance Sheet Data
(In thousands)
(Unaudited)
 
  March 31, 2024  December 31, 2023 
Cash, cash equivalents and investments $749,608  $750,086 
Working capital (1)  732,956   739,834 
Total assets  841,441   843,980 
Total liabilities  95,677   91,977 
Total stockholders’ equity  745,764   752,003 
Restricted cash  2,707   2,707 
         

(1) Working capital is defined as current assets less current liabilities.


FAQ

How much cash, cash equivalents, and investments did Relay Therapeutics have at the end of Q1 2024?

Relay Therapeutics had approximately $750 million in cash, cash equivalents, and investments at the end of Q1 2024.

What is the stock symbol for Relay Therapeutics?

The stock symbol for Relay Therapeutics is RLAY.

What was the revenue for the first quarter of 2024?

The revenue for the first quarter of 2024 was $10.0 million.

What are the anticipated 2024 milestones for Relay Therapeutics?

Anticipated 2024 milestones for Relay Therapeutics include data updates for RLY-2608 and Lirafugratinib in the second half of 2024.

Relay Therapeutics, Inc.

NASDAQ:RLAY

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769.96M
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Biotechnology
Biological Products, (no Disgnostic Substances)
Link
United States of America
CAMBRIDGE