0001564824falseNONE00015648242024-11-062024-11-06
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
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Date of Report (Date of earliest event reported): November 06, 2024 |
Allakos Inc.
(Exact name of Registrant as Specified in Its Charter)
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Delaware |
001-38582 |
45-4798831 |
(State or Other Jurisdiction of Incorporation) |
(Commission File Number) |
(IRS Employer Identification No.) |
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825 Industrial Road, Suite 500 |
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San Carlos, California |
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94070 |
(Address of Principal Executive Offices) |
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(Zip Code) |
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Registrant’s Telephone Number, Including Area Code: 650 597-5002 |
(Former Name or Former Address, if Changed Since Last Report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
☐Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
☐Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
☐Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Securities registered pursuant to Section 12(b) of the Act:
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Title of each class
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Trading Symbol(s) |
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Name of each exchange on which registered
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Common Stock, par value $0.001 |
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ALLK |
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The Nasdaq Global Select Market |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On November 6, 2024, Allakos Inc. (the “Company”) issued a press release reporting its financial results for the third quarter ended September 30, 2024. The full text of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.
The information in this Item 2.02 of this Form 8-K, including the attached Exhibit 99.1, is intended to be furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing made by the Company under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
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Allakos Inc. |
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Date: |
November 6, 2024 |
By: |
/s/ H. Baird Radford, III |
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H. Baird Radford, III Chief Financial Officer |
Exhibit 99.1
Allakos Provides Business Update and Reports Third Quarter 2024 Financial Results
SAN CARLOS, Calif., November 6, 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.
oBioavailability of subcutaneous AK006 was approximately 77%.
oSubcutaneous administered AK006 showed an estimated half-life of 12-22 days.
oConsistent 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.
oThe 720 mg dose of AK006 showed 98% receptor occupancy at day 113 suggesting the potential for infrequent dosing.
oSingle 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
ir@allakos.com
Media Contact:
media@allakos.com
Allakos Inc.
UNAUDITED Statements of Operations and Comprehensive Loss
(in thousands, except per share data)
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Three Months Ended |
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Nine Months Ended |
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September 30, |
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September 30, |
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2024 |
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2023 |
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2024 |
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2023 |
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Operating expenses |
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Research and development |
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$ |
10,874 |
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$ |
36,749 |
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$ |
65,120 |
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$ |
97,107 |
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General and administrative |
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8,876 |
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11,461 |
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28,985 |
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33,966 |
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Impairment of long-lived assets |
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— |
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— |
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27,347 |
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— |
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Total operating expenses |
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19,750 |
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48,210 |
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121,452 |
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131,073 |
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Loss from operations |
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(19,750 |
) |
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(48,210 |
) |
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(121,452 |
) |
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(131,073 |
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Interest income |
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1,392 |
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2,590 |
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5,346 |
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7,965 |
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Other expense, net |
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(14 |
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(6 |
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(88 |
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(42 |
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Net loss |
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(18,372 |
) |
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(45,626 |
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(116,194 |
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(123,150 |
) |
Unrealized gain (loss) on investments |
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325 |
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87 |
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284 |
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212 |
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Comprehensive loss |
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$ |
(18,047 |
) |
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$ |
(45,539 |
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$ |
(115,910 |
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$ |
(122,938 |
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Net loss per common share: |
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Basic and diluted |
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$ |
(0.21 |
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$ |
(0.52 |
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$ |
(1.31 |
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$ |
(1.42 |
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Weighted-average number of common shares outstanding: |
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Basic and diluted |
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89,024 |
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87,115 |
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88,571 |
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86,539 |
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allakos inc.
UNAUDITED CONDENSED balance sheets
(in thousands)
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September 30, |
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December 31, |
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2024 |
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2023 |
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Assets |
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Current assets: |
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Cash and cash equivalents |
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$ |
10,449 |
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$ |
66,440 |
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Investments |
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82,266 |
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104,354 |
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Prepaid expenses and other current assets |
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4,438 |
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9,095 |
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Total current assets |
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97,153 |
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179,889 |
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Property and equipment, net |
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15,733 |
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33,369 |
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Operating lease right-of-use assets |
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9,880 |
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24,136 |
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Other long-term assets |
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1,668 |
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6,216 |
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Total assets |
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$ |
124,434 |
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$ |
243,610 |
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Liabilities and stockholders’ equity |
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Current liabilities: |
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Accounts payable |
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$ |
3,964 |
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$ |
1,764 |
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Accrued expenses and other current liabilities |
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12,017 |
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34,814 |
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Total current liabilities |
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15,981 |
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36,578 |
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Operating lease liabilities, net of current portion |
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35,710 |
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38,215 |
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Total liabilities |
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51,691 |
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74,793 |
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Stockholders’ equity: |
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Common stock |
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89 |
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88 |
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Additional paid-in capital |
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1,306,991 |
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1,287,156 |
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Accumulated other comprehensive gain (loss) |
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334 |
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50 |
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Accumulated deficit |
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(1,234,671 |
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(1,118,477 |
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Total stockholders’ equity |
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72,743 |
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168,817 |
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Total liabilities and stockholders’ equity |
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$ |
124,434 |
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$ |
243,610 |
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v3.24.3
Document And Entity Information
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Nov. 06, 2024 |
Cover [Abstract] |
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Document Type |
8-K
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Amendment Flag |
false
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Document Period End Date |
Nov. 06, 2024
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Entity Registrant Name |
Allakos Inc.
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Entity Central Index Key |
0001564824
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Entity Emerging Growth Company |
false
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Entity File Number |
001-38582
|
Entity Incorporation, State or Country Code |
DE
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Entity Tax Identification Number |
45-4798831
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Entity Address, Address Line One |
825 Industrial Road, Suite 500
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Entity Address, City or Town |
San Carlos
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Entity Address, State or Province |
CA
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Entity Address, Postal Zip Code |
94070
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City Area Code |
650
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Local Phone Number |
597-5002
|
Entity Information, Former Legal or Registered Name |
Not Applicable
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Written Communications |
false
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false
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Pre-commencement Tender Offer |
false
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Pre-commencement Issuer Tender Offer |
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