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    Allakos Provides Business Update and Reports Third Quarter 2024 Financial Results

    11/6/24 4:02:00 PM ET
    $ALLK
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $ALLK alert in real time by email

    SAN CARLOS, Calif., Nov. 06, 2024 (GLOBE NEWSWIRE) -- Allakos Inc. (the "Company") (NASDAQ:ALLK), a biotechnology company developing antibodies for the treatment of allergic, inflammatory and proliferative diseases, today provided a business update and reported financial results for the third quarter ended September 30, 2024.

    Recent Allakos Events

    • Reported safety, pharmacokinetics (PK), and pharmacodynamic (PD) results from the Phase 1 trial of subcutaneous (SC) AK006 in healthy volunteers.
      • Bioavailability of subcutaneous AK006 was approximately 77%.
      • Subcutaneous administered AK006 showed an estimated half-life of 12-22 days.
      • Consistent with the IV formulation, skin biopsies taken from subcutaneous AK006 treated healthy volunteers showed high levels of receptor occupancy confirming AK006 reaches skin tissue mast cells.
      • The 720 mg dose of AK006 showed 98% receptor occupancy at day 113 suggesting the potential for infrequent dosing.
      • Single and multiple doses of IV AK006 and single dose subcutaneous AK006 up to 720 mg were well tolerated with a favorable safety profile.
    • Completed enrollment of over 30 patients in the randomized, double-blind, placebo-controlled Phase 1 trial of intravenous (IV) AK006 in patients with chronic spontaneous urticaria. Data from these patients expected in early Q1 of 2025.

    Upcoming Allakos Anticipated Milestones

    • Report randomized double-blind, placebo-controlled data on over 30 patients from the Phase 1 trial of AK006 in patients with CSU in early Q1 of 2025.

    Cash Guidance

    Allakos ended the third quarter of 2024 with $92.7 million in cash, cash equivalents and investments. Allakos' financial outlook, restructuring activities and estimated cash runway as reported by the Company in January 2024 remain unchanged. The Company reiterates that it expects the restructuring activities will extend the cash runway into mid-2026 and to end 2024 with total cash, cash equivalents and investments in its previously stated $81 to $86 million guidance range. The Company has substantially completed its exit of the lirentelimab development program.

    Third Quarter 2024 Financial Results

    Allakos ended the third quarter of 2024 with $92.7 million in cash, cash equivalents and investments resulting in a net decrease in cash, cash equivalents and investments of $30.4 million during the third quarter of 2024. Approximately $18 million of this third quarter decrease was paid in connection with exiting the lirentelimab development program.

    Research and development expenses were $10.9 million in the third quarter of 2024 compared to $36.7 million in the third quarter of 2023, a decrease of $25.8 million. This quarter over quarter decrease is attributed to $16.4 million of lower contract research and development costs, primarily due to halting lirentelimab development and includes a $4.6 million decrease relating to a change in estimated manufacturing costs upon resolution of the related work orders with the vendor, $5.7 million of decreased compensation costs and a $3.7 million decrease in other research and development expenses.

    General and administrative expenses were $8.9 million for the third quarter of 2024 compared to $11.5 million for the third quarter of 2023, a decrease of $2.6 million. The quarter over quarter change included $2.4 million of decreased compensation costs and $0.2 million of decreased other general and administrative expenses.

    Allakos reported a net loss of $18.4 million in the third quarter of 2024 compared to $45.6 million in the third quarter of 2023. Net loss per basic and diluted share was $0.21 for the third quarter of 2024 compared to $0.52 in the third quarter of 2023.

    About Allakos

    Allakos is a clinical stage biotechnology company developing therapeutics that target immunomodulatory receptors present on immune effector cells involved in allergy, inflammatory and proliferative diseases. Activating these immunomodulatory receptors allows for the direct targeting of cells involved in disease pathogenesis and, in the setting of allergy and inflammation, has the potential to result in broad inhibition of inflammatory cells. The Company's most advanced product candidate is AK006. AK006 targets Siglec-6, an inhibitory receptor expressed on mast cells. Mast cells are widely distributed in the body and play a central role in the inflammatory response. Inappropriately activated mast cells have been identified as key drivers in a number of severe diseases affecting the gastrointestinal tract, eyes, skin, lungs and other organs. In preclinical studies, AK006 appears to provide deep mast cell inhibition and, in addition to its inhibitory activity, reduce mast cell numbers. For more information, please visit the Company's website at www.allakos.com.

    Forward-Looking Statements

    This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 as contained in Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Such forward-looking statements include, but are not limited to, Allakos' expected timing of reporting data from its clinical trial of AK006; cash guidance and runway; and restructuring. Such statements are subject to numerous important factors, risks and uncertainties that may cause actual events or results to differ materially from current expectations and beliefs, including but not limited to: Allakos' stages of clinical drug development; Allakos' ability to timely initiate and complete clinical trials for AK006; Allakos' ability to obtain required regulatory approvals for its clinical trials; uncertainties related to the enrollment of patients in its clinical trials; Allakos' ability to demonstrate sufficient safety and efficacy of its product candidates in its clinical trials; uncertainties related to the success of clinical trials, regardless of the outcomes of preclinical testing or early-stage trials; Allakos' ability to obtain regulatory approvals to market its product candidates; market acceptance of Allakos' product candidates; uncertainties related to the projections of the size of patient populations suffering from the diseases Allakos is targeting; Allakos' ability to advance additional product candidates beyond AK006; uncertainties related to Allakos' ability to realize the contemplated benefits of its restructuring and related reduction in force; Allakos' ability to accurately forecast financial results; Allakos' ability to obtain additional capital to finance its operations, research and drug development; Allakos' ability to maintain the listing of our common stock on Nasdaq; general economic and market conditions, both domestic and international; domestic and international regulatory obligations; and other risks. Information regarding the foregoing and additional risks may be found in the section entitled "Risk Factors" in documents that Allakos files from time to time to with the SEC. These documents contain and identify important factors that could cause the actual results for Allakos to differ materially from those contained in Allakos' forward-looking statements. Any forward-looking statements contained in this press release speak only as of the date hereof, and Allakos specifically disclaims any obligation to update any forward-looking statement, except as required by law. These forward-looking statements should not be relied upon as representing Allakos' views as of any date subsequent to the date of this press release.

    Source: Allakos Inc.

    Investor Contact:

    Adam Tomasi, President

    Alex Schwartz, VP Strategic Finance and Investor Relations

    [email protected]

    Media Contact:

    [email protected]

    ALLAKOS INC.
    UNAUDITED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
    (in thousands, except per share data)
     
      Three Months Ended  Nine Months Ended 
      September 30,  September 30, 
      2024  2023  2024  2023 
    Operating expenses            
    Research and development $10,874  $36,749  $65,120  $97,107 
    General and administrative  8,876   11,461   28,985   33,966 
    Impairment of long-lived assets  —   —   27,347   — 
    Total operating expenses  19,750   48,210   121,452   131,073 
    Loss from operations  (19,750)  (48,210)  (121,452)  (131,073)
    Interest income  1,392   2,590   5,346   7,965 
    Other expense, net  (14)  (6)  (88)  (42)
    Net loss  (18,372)  (45,626)  (116,194)  (123,150)
    Unrealized gain (loss) on investments  325   87   284   212 
    Comprehensive loss $(18,047) $(45,539) $(115,910) $(122,938)
    Net loss per common share:            
    Basic and diluted $(0.21) $(0.52) $(1.31) $(1.42)
    Weighted-average number of common

    shares outstanding:
                
    Basic and diluted  89,024   87,115   88,571   86,539 
     



    ALLAKOS INC.
    UNAUDITED CONDENSED BALANCE SHEETS
    (in thousands)
     
      September 30,  December 31, 
      2024  2023 
    Assets

          
    Current assets:      
    Cash and cash equivalents $10,449  $66,440 
    Investments  82,266   104,354 
    Prepaid expenses and other current assets  4,438   9,095 
    Total current assets  97,153   179,889 
    Property and equipment, net  15,733   33,369 
    Operating lease right-of-use assets  9,880   24,136 
    Other long-term assets  1,668   6,216 
    Total assets $124,434  $243,610 
    Liabilities and stockholders' equity

          
    Current liabilities:      
    Accounts payable $3,964  $1,764 
    Accrued expenses and other current liabilities  12,017   34,814 
    Total current liabilities  15,981   36,578 
    Operating lease liabilities, net of current portion  35,710   38,215 
    Total liabilities  51,691   74,793 
    Stockholders' equity:      
    Common stock  89   88 
    Additional paid-in capital  1,306,991   1,287,156 
    Accumulated other comprehensive gain (loss)  334   50 
    Accumulated deficit  (1,234,671)  (1,118,477)
     Total stockholders' equity  72,743   168,817 
    Total liabilities and stockholders' equity $124,434  $243,610 
     


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    Q&A

    New
    • What was the cash position of Allakos Inc. at the end of Q3 2024?

      Allakos Inc. ended Q3 2024 with $92.7 million in cash and equivalents after a net decrease of $30.4 million during the quarter, largely due to costs related to restructuring and exiting the lirentelimab development program.

    • What were the key pharmacokinetic findings from the AK006 Phase 1 trial?

      The Phase 1 trial of AK006 indicated that the subcutaneous version has a bioavailability of about 77% and an estimated half-life of 12-22 days, which suggests potential for infrequent dosing.

    • What is the anticipated timeline for reporting data from the ongoing AK006 trial?

      Allakos aims to report data from over 30 patients in the ongoing Phase 1 trial of intravenous AK006 for chronic spontaneous urticaria in early Q1 2025.

    • How did Allakos' net loss in Q3 2024 compare to the previous year?

      In Q3 2024, Allakos reported a net loss of $18.4 million, a significant reduction compared to the $45.6 million loss reported in Q3 2023, indicating improved financial performance year-over-year.

    • What is the expected impact of Allakos' restructuring activities on its cash runway?

      The restructuring activities are projected to extend the cash runway into mid-2026, while the company expects to end 2024 with total cash and equivalents between $81 million and $86 million.

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