PART I FINANCIAL INFORMATION Item 1 Financial Statements (Unaudited) The unaudited financial statements reveal a decrease in total assets and stockholders' equity, alongside significant net losses driven by increased R&D expenses Condensed Consolidated Balance Sheets Condensed Consolidated Balance Sheets (in thousands) | Metric | June 30, 2022 | December 31, 2021 | | :---------------------------------- | :-------------- | :------------------ | | Assets | | | | Cash and cash equivalents | $66,378 | $363,667 | | Short-term investments | $246,988 | — | | Total current assets | $316,847 | $367,019 | | Total assets | $346,018 | $380,183 | | Liabilities and Stockholders' Equity | | | | Total current liabilities | $23,952 | $15,295 | | Total liabilities | $29,699 | $17,134 | | Total stockholders' equity | $316,319 | $363,049 | | Total liabilities and stockholders' equity | $346,018 | $380,183 | - Total assets decreased from $380.2 million at December 31, 2021, to $346.0 million at June 30, 2022, primarily due to a significant reduction in cash and cash equivalents, partially offset by new short-term investments9 - Total stockholders' equity decreased from $363.0 million at December 31, 2021, to $316.3 million at June 30, 2022, mainly due to accumulated deficit and unrealized losses on available-for-sale investments10 Condensed Consolidated Statements of Operations Condensed Consolidated Statements of Operations (in thousands, except per share amounts) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :--------------------------------------------------------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Research and development | $26,748 | $11,213 | $43,821 | $21,062 | | General and administrative | $7,041 | $5,086 | $14,715 | $9,445 | | Total operating expenses | $33,789 | $16,299 | $58,536 | $30,507 | | Loss from operations | $(33,789) | $(16,299) | $(58,536) | $(30,507) | | Interest income | $876 | $23 | $1,101 | $48 | | Net loss | $(32,920) | $(16,274) | $(57,453) | $(30,459) | | Net loss per share, basic and diluted | $(0.81) | $(0.40) | $(1.41) | $(0.76) | | Weighted-average shares of common stock used to compute net loss per shares, basic and diluted | 40,687,751 | 40,247,110 | 40,652,224 | 40,151,802 | - Net loss for the three months ended June 30, 2022, increased to $32.9 million from $16.3 million in the prior year, a 102% increase, primarily due to higher operating expenses1264 - Net loss for the six months ended June 30, 2022, increased to $57.5 million from $30.5 million in the prior year, an 89% increase1264 - Research and development expenses significantly increased by 139% for the three months and 108% for the six months ended June 30, 2022, compared to the same periods in 20211264 Condensed Consolidated Statements of Comprehensive Loss Condensed Consolidated Statements of Comprehensive Loss (in thousands) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :---------------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Net loss | $(32,920) | $(16,274) | $(57,453) | $(30,459) | | Unrealized loss on available-for-sale investments | $(650) | — | $(1,256) | — | | Total comprehensive loss | $(33,570) | $(16,274) | $(58,709) | $(30,459) | - Total comprehensive loss for the three months ended June 30, 2022, was $33.6 million, including an unrealized loss of $0.7 million on available-for-sale investments, compared to $16.3 million in the prior year with no such loss14 - For the six months ended June 30, 2022, total comprehensive loss was $58.7 million, including an unrealized loss of $1.3 million on available-for-sale investments, compared to $30.5 million in the prior year14 Condensed Consolidated Statements of Stockholders' Equity Condensed Consolidated Statements of Stockholders' Equity (in thousands, except share amounts) | Metric | Common Shares (June 30, 2022) | Common Stock Amount (June 30, 2022) | Additional Paid-In Capital (June 30, 2022) | Accumulated Other Comprehensive Loss (June 30, 2022) | Accumulated Deficit (June 30, 2022) | Total Stockholders' Equity (June 30, 2022) | | :---------------------------------------- | :---------------------------- | :-------------------------- | :--------------------------------------- | :--------------------------------------- | :---------------------------------- | :--------------------------------------- | | Balance as of December 31, 2021 | 40,587,067 | $41 | $564,993 | $0 | $(201,985) | $363,049 | | Issuance of common stock under equity incentive plans | 114,183 | $0 | $340 | $0 | $0 | $340 | | Issuance of common stock under employee stock purchase plan | 44,002 | $0 | $302 | $0 | $0 | $302 | | Stock-based compensation | — | $0 | $11,337 | $0 | $0 | $11,337 | | Unrealized loss on available-for-sale investments | — | $0 | $0 | $(1,256) | $0 | $(1,256) | | Net loss | — | $0 | $0 | $0 | $(57,453) | $(57,453) | | Balance as of June 30, 2022 | 40,745,252 | $41 | $576,972 | $(1,256) | $(259,438) | $316,319 | - Total stockholders' equity decreased from $363.0 million at December 31, 2021, to $316.3 million at June 30, 2022, primarily due to a net loss of $57.5 million and an accumulated other comprehensive loss of $1.3 million16 - Additional paid-in capital increased by $11.9 million, driven by stock-based compensation of $11.3 million and proceeds from equity incentive plans and employee stock purchase plans16 Condensed Consolidated Statements of Cash Flows Condensed Consolidated Statements of Cash Flows (in thousands) | Metric | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :-------------------------------------------------------------------------- | :----------------------------- | :----------------------------- | | Net cash used in operating activities | $(37,672) | $(25,757) | | Net cash used in investing activities | $(260,053) | $(7) | | Net cash provided by financing activities | $502 | $1,509 | | Net decrease in cash, cash equivalents and restricted cash | $(297,223) | $(24,255) | | Cash, cash equivalents and restricted cash at end of period | $66,444 | $409,964 | - Net cash used in operating activities increased to $37.7 million for the six months ended June 30, 2022, from $25.8 million in the prior year, driven by a higher net loss1871 - Net cash used in investing activities significantly increased to $260.1 million for the six months ended June 30, 2022, primarily due to purchases of short-term and long-term investments1874 - Net cash provided by financing activities decreased to $0.5 million for the six months ended June 30, 2022, from $1.5 million in the prior year1875 Notes to Condensed Consolidated Financial Statements (1) ORGANIZATION - ALX Oncology Holdings Inc is a clinical-stage immuno-oncology company focused on developing therapies that block the CD47 checkpoint pathway to fight cancer20 - The Company has not realized product revenues and expects to incur additional losses, planning to raise capital through equity sales, debt financings, or strategic alliances20 - Management believes existing capital resources are sufficient to fund projected operating requirements for at least the next twelve months20 (2) SIGNIFICANT ACCOUNTING POLICIES - The unaudited condensed consolidated financial statements are prepared in accordance with GAAP and SEC interim reporting rules, with certain disclosures condensed or omitted21 - The Company's investments are classified as available-for-sale, carried at fair value, and include money market funds, U.S. Treasury securities, corporate debt, commercial paper, and asset-backed securities24 - No new or material changes to significant accounting policies were reported, except for the policy on Investments23 (3) FAIR VALUE OF FINANCIAL INSTRUMENTS Fair Value of Cash Equivalents and Available-for-Sale Investments (in thousands) | Metric | June 30, 2022 | December 31, 2021 | | :-------------------------------- | :-------------- | :------------------ | | Cash and cash equivalents | $55,205 | $357,181 | | Short-term investments | $246,988 | — | | Long-term investments | $10,860 | — | | Total | $313,053 | $357,181 | - The Company classifies financial assets into Level 1 (quoted prices in active markets) and Level 2 (observable inputs other than active market prices) of the fair value hierarchy25 - As of June 30, 2022, unrealized losses on available-for-sale investments were non-credit related, and the Company does not intend to sell these investments before recovery of their amortized cost basis29 (4) BALANCE SHEET COMPONENTS Property and Equipment, Net (in thousands) | Metric | June 30, 2022 | December 31, 2021 | | :---------------------------------------- | :-------------- | :------------------ | | Property and equipment, gross | $1,835 | $960 | | Less: accumulated depreciation and amortization | $(205) | $(63) | | Property and equipment, net | $1,630 | $897 | Other Assets (in thousands) | Metric | June 30, 2022 | December 31, 2021 | | :---------------------------------------- | :-------------- | :------------------ | | Long-term prepaid clinical expenses | $7,012 | $6,694 | | Operating lease right-of-use assets | $6,083 | $1,829 | | Total other assets | $16,681 | $12,267 | Accrued Expenses and Other Current Liabilities (in thousands) | Metric | June 30, 2022 | December 31, 2021 | | :---------------------------------------- | :-------------- | :------------------ | | Accrued clinical and nonclinical study costs | $4,237 | $4,125 | | Accrued contract manufacturing | $2,811 | $693 | | Total accrued expenses and other current liabilities | $12,747 | $9,901 | (5) LEASES - The Company has operating leases for office and laboratory space in South San Francisco and Palo Alto, California, and finance leases for pharmaceutical support services equipment3334 Total Lease Costs (in thousands) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :---------------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Operating lease cost | $271 | $62 | $520 | $97 | | Finance lease cost | $114 | $93 | $229 | $151 | | Total lease costs | $515 | $172 | $975 | $287 | - Operating lease costs significantly increased for both the three and six months ended June 30, 2022, primarily due to the expansion of new laboratory space36 (6) STOCKHOLDERS' EQUITY - As of June 30, 2022, the Company had 40,745,252 shares of common stock outstanding, with 11,213,603 shares reserved for future issuance under equity incentive plans and the Employee Stock Purchase Plan3940 (7) STOCK-BASED COMPENSATION - The 2020 Equity Incentive Plan and Employee Stock Purchase Plan shares increased on January 1, 2022, providing more shares for future issuance41 Stock-based Compensation Expense (in thousands) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :-------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Research and development | $2,690 | $715 | $4,765 | $1,294 | | General and administrative | $3,146 | $1,522 | $6,572 | $2,743 | | Total | $5,836 | $2,237 | $11,337 | $4,037 | - Total stock-based compensation expense increased significantly to $5.8 million for the three months and $11.3 million for the six months ended June 30, 2022, compared to the prior year periods42 (8) RELATED-PARTY TRANSACTIONS - The Company has a research and development services agreement and a collaboration agreement with Tallac Therapeutics, Inc, for preclinical research and joint development of a novel cancer immunotherapy (ALTA-002)4546 - R&D costs related to the Tallac Collaboration Agreement increased to $2.5 million for the three months and $3.7 million for the six months ended June 30, 2022, from $0.6 million for both periods in 202146 (9) NET LOSS PER SHARE Net Loss Per Share (in thousands, except per share data) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :---------------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Net loss | $(32,920) | $(16,274) | $(57,453) | $(30,459) | | Net loss per share, basic and diluted | $(0.81) | $(0.40) | $(1.41) | $(0.76) | | Weighted-average shares outstanding, basic and diluted | 40,687,751 | 40,247,110 | 40,652,224 | 40,151,802 | - Basic and diluted net loss per share were the same for all periods presented due to the Company being in a loss position, making potential common stock anti-dilutive48 - Potentially dilutive securities, including stock options and restricted stock, totaling 5.7 million shares as of June 30, 2022, were excluded from diluted EPS calculation49 (10) COMMITMENTS AND CONTINGENCIES - The Company has contractual obligations for manufacturing and service contracts totaling approximately $49.2 million as of June 30, 2022, primarily for evorpacept clinical trials5276 - No pending or threatened material legal proceedings were reported as of June 30, 202251 (11) SUBSEQUENT EVENTS - The Company did not identify any subsequent events requiring adjustment or disclosure in the financial statements up to the date of issuance54 Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations Management discusses the financial condition and results, highlighting increased operating losses from R&D, the current liquidity position, and future funding needs Overview - ALX Oncology is a clinical-stage immuno-oncology company developing therapies that block the CD47 checkpoint pathway, with evorpacept as its lead product candidate in multiple Phase 1 and 2 clinical trials56 - Evorpacept has received FDA Fast Track designation for first-line advanced HNSCC and HER2-overexpressing gastric/GEJ cancer, and Orphan Drug Designation for gastric/GEJ cancer and AML56 - The Company has incurred significant net losses since inception, with $57.5 million for the six months ended June 30, 2022, and expects increasing operating losses as it advances product candidates and expands operations57 Components of Results of Operations Research and Development Expenses - R&D expenses primarily consist of costs for evorpacept development, including preclinical and clinical development, employee-related expenses, clinical material production, and laboratory/vendor expenses58 - The Company expenses R&D costs as incurred and expects them to increase substantially due to advancing existing and developing new product candidates, and conducting larger clinical trials59 General and Administrative Expenses - G&A expenses include personnel-related costs, business development, facilities, depreciation, and professional services, expected to increase with headcount, infrastructure, and public company compliance60 Interest Income - Interest income is primarily derived from cash, cash equivalents, and short-term and long-term investments61 Other Income (Expense), Net - Other income (expense), net, primarily consists of interest expense on finance leases62 Results of Operations Summary of Results of Operations (in thousands) | Metric | Three Months Ended June 30, 2022 | Three Months Ended June 30, 2021 | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :---------------------------------- | :------------------------------- | :------------------------------- | :----------------------------- | :----------------------------- | | Research and development | $26,748 | $11,213 | $43,821 | $21,062 | | General and administrative | $7,041 | $5,086 | $14,715 | $9,445 | | Total operating expenses | $33,789 | $16,299 | $58,536 | $30,507 | | Net loss | $(32,920) | $(16,274) | $(57,453) | $(30,459) | - Research and development expenses increased by $15.5 million (139%) for the three months and $22.8 million (108%) for the six months ended June 30, 2022, primarily due to increased clinical and development costs, personnel, and stock-based compensation6365 - General and administrative expenses increased by $2.0 million (38%) for the three months and $5.3 million (56%) for the six months ended June 30, 2022, mainly due to higher stock-based compensation and headcount growth6667 Liquidity and Capital Resources - As of June 30, 2022, the Company had $324.2 million in cash, cash equivalents, and short-term and long-term investments66 - The Company believes existing capital resources are sufficient to fund operating expenses and capital expenditure requirements through the fourth quarter of 202469 - Future funding will be required through equity offerings, debt financings, collaborations, or licensing arrangements, with no committed external sources currently91 Summary of Net Cash Flow Activity (in thousands) | Metric | Six Months Ended June 30, 2022 | Six Months Ended June 30, 2021 | | :-------------------------------------------------------------------------- | :----------------------------- | :----------------------------- | | Net cash used in operating activities | $(37,672) | $(25,757) | | Net cash used in investing activities | $(260,053) | $(7) | | Net cash provided by financing activities | $502 | $1,509 | | Net decrease in cash, cash equivalents and restricted cash | $(297,223) | $(24,255) | Contractual Obligations and Commitments as of June 30, 2022 (in thousands) | Type | Total | 2022 (remaining 6 months) | 2023-2024 | 2025-2026 | Thereafter | | :-------------------------------- | :------ | :------------------------ | :-------- | :-------- | :--------- | | Operating lease obligations | $8,572 | $549 | $2,519 | $2,504 | $3,000 | | Finance lease obligations | $504 | $216 | $288 | — | — | | Manufacturing and service contracts | $49,150 | $17,205 | $31,727 | $218 | — | | Total | $58,226 | $17,970 | $34,534 | $2,722 | $3,000 | Critical Accounting Policies and Significant Judgments and Estimates - The Company's financial statements rely on estimates and assumptions, particularly for long-lived assets, clinical trial accruals, fair value measurements, income taxes, and stock-based compensation79 - No material changes to critical accounting policies were reported during the six months ended June 30, 2022, from those discussed in the 2021 Annual Report on Form 10-K79 Recent Accounting Pronouncements - No new accounting pronouncements were identified that would have a material impact on the Company's financial statements2580 Item 3 Quantitative and Qualitative Disclosures about Market Risk The Company's market risk exposure is primarily from interest rates, credit, and foreign currency, though these are not currently considered material Interest Rate Risk - The Company's primary market risk exposure is interest rate sensitivity, with $324.2 million in cash, cash equivalents, and investments as of June 30, 202281 - An immediate 100 basis point change in interest rates would not materially affect the fair market value of the Company's cash, cash equivalents, and investments81 Credit Risk - The Company's financial instruments, including cash, cash equivalents, and investments, are subject to credit risk, but investments are limited to highly rated corporate entities and government securities82 - No realized losses on deposits or investments have been experienced during the periods presented82 Foreign Currency Risk - The Company has limited exposure to foreign currency risk from contracts denominated primarily in Euro, but foreign currency transaction gains and losses have not been material83 - A 10.0% increase or decrease in current exchange rates would not have a material effect on financial results83 Item 4 Controls and Procedures Management concluded that the Company's disclosure controls and procedures were effective as of June 30, 2022, with no material changes in internal control Evaluation of Disclosure Controls and Procedures - Management, including the CEO and CFO, concluded that disclosure controls and procedures were effective as of June 30, 2022, ensuring timely and accurate reporting8485 Changes in Internal Control over Financial Reporting - No material changes in internal control over financial reporting occurred during the quarter ended June 30, 202286 PART II OTHER INFORMATION Item 1 Legal Proceedings The Company is not currently involved in any material legal proceedings, though it may encounter ordinary course claims that could negatively impact the business - The Company is not currently a party to any material legal proceedings87 - Litigation, if it arises, could adversely impact the business due to defense and settlement costs, diversion of management resources, and reputational harm87 Item 1A Risk Factors The Company faces significant risks in its financial position, product development, regulatory environment, intellectual property, and operational challenges Risk Factors Summary - Key risks include significant net losses, the need for substantial additional capital, limited operating history, stock price volatility, and heavy dependence on the success of evorpacept89 - Other risks involve the unpredictability of clinical trial outcomes, potential adverse events, regulatory approval challenges, intellectual property protection, reliance on key personnel and third parties, and the impact of the COVID-19 pandemic89 Risks Related to Our Financial Position and Need for Additional Capital - The Company has incurred significant net losses since inception ($259.4 million accumulated deficit as of June 30, 2022) and expects to continue incurring losses for the foreseeable future90 - Substantial additional capital will be required to finance operations, and failure to raise it on acceptable terms could lead to delays or elimination of R&D programs91 - The Company has a limited operating history and no products approved for commercial sale, making it difficult to evaluate its likelihood of success and viability91 Risks Related to the Discovery, Development and Commercialization of Our Product Candidates - The Company is substantially dependent on the success of its lead product candidate, evorpacept, which is in clinical development and has not completed a pivotal trial93 - Preclinical and early clinical trial outcomes may not predict success in later trials, and clinical trials are expensive, time-consuming, and may fail to demonstrate adequate safety or efficacy9394 - Product candidates may cause significant adverse events or undesirable side effects, potentially preventing regulatory approval, limiting commercial potential, or leading to market withdrawal96 - The Company faces substantial competition from major pharmaceutical and biotechnology companies developing immuno-oncology therapies, including those targeting the CD47 pathway9899 - Reliance on third parties for manufacturing and clinical trials increases risks of insufficient supply, quality issues, and delays102104 Risks Related to Government Regulation - Even if product candidates receive regulatory approval, they will be subject to significant ongoing post-marketing regulatory requirements and oversight, leading to additional expenses108 - The regulatory approval processes are lengthy, time-consuming, and unpredictable, potentially preventing the Company from generating product revenue or commercializing products outside the U.S109 - Failure to obtain or maintain adequate coverage and reimbursement for approved products could limit marketability and revenue generation106 - Business operations are subject to federal and state healthcare fraud and abuse laws, false claims laws, and health information privacy and security laws, with non-compliance leading to substantial penalties113 - Data collection and transfer are governed by restrictive regulations like GDPR, UK GDPR, and CCPA, increasing compliance costs and potential liability115116 Risks Related to Intellectual Property - Inability to obtain, maintain, and enforce patent protection for product candidates and related technology could materially harm the business117 - Patent protection may be inadequate globally, and changes in patent laws or jurisprudence could diminish the value of patents118119 - The Company may become involved in lawsuits to protect or enforce patents and trade secrets, which are expensive, time-consuming, and may be unsuccessful122 - Commercial success depends on operating without infringing third-party intellectual property rights, and the Company may be subject to claims of infringement123 Risks Related to Our Operations - The Company needs to grow its organization and may experience difficulties managing this growth, including recruiting and retaining qualified personnel127129 - International operations expose the Company to business, regulatory, political, operational, financial, pricing, and reimbursement risks131 - Reliance on third parties for operational and administrative services, and potential system failures or security breaches, could adversely affect the business133150152 - The ongoing COVID-19 pandemic continues to adversely impact business, clinical trials, and preclinical research, causing potential delays and increased costs134135 Risks Related to Ownership of Our Common Stock - The trading market for common stock may not be sustained, and future sales of shares could cause the stock price to fall due to dilution141145 - The stock price may be highly volatile due to various factors, including clinical trial results, regulatory developments, competition, and macroeconomic conditions142143 - The Company incurs significant increased costs and management resources as a public company, especially after no longer qualifying as an 'emerging growth company'146147 - Principal stockholders and management own a significant percentage of stock, allowing them to exert substantial control over matters subject to stockholder approval148 General Risks - Business disruptions from natural disasters, public health crises, or man-made events could seriously harm future revenue and financial condition151 - System failures or security breaches could lead to data loss, delays in regulatory approval, increased costs, and reputational damage152153 - Disclosure controls and procedures may not prevent or detect all errors or acts of fraud, potentially leading to misstated financial reports154 Item 2 Unregistered Sales of Equity Securities and Use of Proceeds No unregistered sales of equity securities or issuer purchases occurred, and IPO proceeds were invested according to policy with no change in planned use - Proceeds from the initial public offering were invested in accordance with the Company's investment policy, with no material change in planned use156 - No unregistered sales of equity securities or issuer purchases of equity securities occurred during the period156 Item 3 Defaults Upon Senior Securities This item is not applicable to the Company for the reporting period - This item is not applicable157 Item 4 Mine Safety Disclosures This item is not applicable to the Company for the reporting period - This item is not applicable157 Item 5 Other Information No other information is reported under this item - No other information is reported157 Item 6 Exhibits This section lists the exhibits filed with the Quarterly Report, including officer certifications and Inline XBRL documents - Exhibits include certifications from the Principal Executive Officer and Principal Financial Officer (31.1, 31.2, 32.1, 32.2) and various Inline XBRL documents (101.INS, 101.SCH, 101.CAL, 101.DEF, 101.LAB, 101.PRE, 104)158159 SIGNATURES - The report is signed by Jaume Pons, Ph.D. (President and CEO), Peter Garcia (CFO), and Shelly Pinto (VP, Finance and Chief Accounting Officer) on August 8, 2022161
ALX Oncology(ALXO) - 2022 Q2 - Quarterly Report