
PART I. FINANCIAL INFORMATION Financial Statements The unaudited condensed consolidated financial statements for Immix Biopharma, Inc. as of June 30, 2025, and for the three and six months ended June 30, 2025 and 2024, detail the company's financial position, operational results, changes in equity, and cash flows, reflecting increased net losses and a decrease in cash reserves, primarily driven by escalating research and development expenses for its clinical programs Condensed Consolidated Balance Sheets The balance sheet as of June 30, 2025, shows a significant decrease in cash and cash equivalents to $11.6 million from $17.7 million at year-end 2024, with total assets declining to $15.6 million from $22.9 million, while total liabilities increased to $11.0 million, and total stockholders' equity fell sharply to $4.7 million from $13.3 million, reflecting the company's net loss and cash burn Condensed Consolidated Balance Sheet Highlights (Unaudited) | Balance Sheet Item | June 30, 2025 (USD) | December 31, 2024 (USD) | | :--- | :--- | :--- | | Cash and cash equivalents | $11,637,945 | $17,681,954 | | Total current assets | $12,325,460 | $20,197,834 | | Total assets | $15,635,104 | $22,947,872 | | Total current liabilities | $10,009,738 | $8,687,118 | | Total liabilities | $10,982,073 | $9,696,669 | | Total stockholders' equity | $4,653,031 | $13,251,203 | Condensed Consolidated Statements of Operations and Comprehensive Loss The company reported a net loss of $6.6 million for the three months ended June 30, 2025, a 50% increase from the $4.4 million loss in the same period of 2024, and for the six-month period, the net loss was $11.2 million in 2025 compared to $9.7 million in 2024, with widening losses primarily due to a substantial increase in research and development expenses Statement of Operations Highlights (Unaudited) | Metric | Three Months Ended June 30, 2025 (USD) | Three Months Ended June 30, 2024 (USD) | Six Months Ended June 30, 2025 (USD) | Six Months Ended June 30, 2024 (USD) | | :--- | :--- | :--- | :--- | :--- | | Research and development | $3,972,458 | $2,224,139 | $5,947,532 | $5,472,808 | | General and administrative | $2,745,247 | $2,478,357 | $5,453,098 | $4,819,821 | | Loss from operations | ($6,717,705) | ($4,702,496) | ($11,400,630) | ($10,292,629) | | Net loss | ($6,622,563) | ($4,405,850) | ($11,165,091) | ($9,736,914) | | Loss per common share | ($0.22) | ($0.15) | ($0.37) | ($0.36) | Condensed Consolidated Statements of Stockholders' Equity Stockholders' equity decreased from $13.3 million at the end of 2024 to $4.7 million as of June 30, 2025, primarily driven by the net loss of $11.2 million for the six-month period, partially offset by capital raised from stock issuances under the At-The-Market (ATM) facility - For the six months ended June 30, 2025, the company's total stockholders' equity decreased by approximately $8.6 million, from $13,251,203 to $4,653,03119 - The decrease in equity was primarily due to a net loss of $11,165,091, which was partially offset by proceeds from stock issuances, including $1,094,399 net from the ATM facility1619 Condensed Consolidated Statements of Cash Flows For the six months ended June 30, 2025, net cash used in operating activities was $7.0 million, with $1.1 million generated from financing activities, primarily through its ATM offering, resulting in a net decrease in cash and cash equivalents of $6.0 million, leaving an ending balance of $11.6 million Cash Flow Summary (Six Months Ended June 30) | Cash Flow Activity | 2025 (USD) | 2024 (USD) | | :--- | :--- | :--- | | Net cash used in operating activities | ($6,994,921) | ($9,082,817) | | Net cash used in investing activities | ($195,343) | ($398,987) | | Net cash provided by financing activities | $1,110,116 | $15,948,567 | | Net change in cash and cash equivalents | ($6,044,009) | $6,465,307 | | Cash and cash equivalents – end of period | $11,637,945 | $23,975,098 | Notes to the Condensed Consolidated Financial Statements (Unaudited) The notes provide critical context to the financial statements, highlighting the company's clinical-stage nature, significant accounting policies, and major financial events, including details on financing activities, such as the ATM agreement and a CIRM grant, license agreements with ongoing payment obligations, and a 'going concern' warning due to recurring losses and insufficient capital to fund operations for the next twelve months - The company is a clinical-stage biopharmaceutical firm focused on developing cell therapies for AL Amyloidosis and other diseases25 - Management has concluded there is substantial doubt about the Company's ability to continue as a going concern, as it does not have sufficient capital to sustain operations for at least the next twelve months from the filing date39 - In June 2025, the company initiated an At The Market (ATM) offering agreement to sell up to $50 million of its common stock, and as of June 30, 2025, it had raised net proceeds of $1.1 million under this agreement38 - The company was awarded an $8 million grant from CIRM in July 2024 and has received $3.6 million in reimbursements as of June 30, 2025, with the remaining $4.4 million contingent on achieving milestones3787 - The company has significant financial commitments under a license agreement with HADASIT and BIRAD, including quarterly payments totaling approximately $13.0 million due through September 2026, plus potential royalties and milestone payments83 Management's Discussion and Analysis of Financial Condition and Results of Operations Management discusses the company's focus on its lead CAR-T candidate, NXC-201, for AL Amyloidosis, highlighting recent positive clinical data and regulatory designations like RMAT, with the analysis of financial results showing widening net losses due to increased R&D spending on clinical trials, and the liquidity section underscoring a 'going concern' issue, stating that current cash is insufficient for the next year and detailing plans to raise additional capital through its ATM facility and other means Overview Immix Biopharma is a clinical-stage company focused on developing its lead CAR-T cell therapy candidate, NXC-201, for AL Amyloidosis and other serious diseases, with NXC-201 having received FDA RMAT and ODD designations, and recent clinical data from ongoing trials presented at major conferences (ASH, ASCO) showing high overall and complete response rates in relapsed/refractory AL Amyloidosis patients - The company's lead candidate, NXC-201, is a CAR-T therapy for AL Amyloidosis that has received FDA Regenerative Medicine Advanced Therapy (RMAT) and Orphan Drug Designation (ODD)106107 - Clinical data presented at ASCO 2025 for 10 patients showed a 70% complete response (CR) rate, with all patients normalizing pathological disease markers and no relapses recorded123 - The company is conducting two clinical trials for NXC-201 in AL Amyloidosis: the U.S.-based Phase 1b/2 NEXICART-2 and the ex-U.S. Phase 1b/2a NEXICART-1116 Results of Operations Comparing the periods ended June 30, 2025, and 2024, the company's net loss increased for both the three-month and six-month periods, primarily driven by a significant rise in Research and Development expenses, which grew from $2.2 million to $4.0 million for the second quarter, due to costs associated with the ongoing CAR-T clinical trials, while General and Administrative expenses also saw a moderate increase Comparison of Operating Expenses (Three Months Ended June 30) | Expense Category | 2025 (USD) | 2024 (USD) | Change (USD) | | :--- | :--- | :--- | :--- | | General and administrative | $2,745,247 | $2,478,357 | +$266,890 | | Research and development | $3,972,458 | $2,224,139 | +$1,748,319 | - The increase in R&D expense was primarily driven by costs for the ongoing Phase 1b/2a CAR-T clinical trial, including patient treatment, site onboarding, and license fees136 - Net loss for Q2 2025 was $6.6 million, compared to $4.4 million in Q2 2024, mainly due to the increase in R&D expenses139 Liquidity and Capital Resources As of June 30, 2025, the company had $11.6 million in cash and cash equivalents, but management states these funds are not sufficient to support planned operations for the next twelve months, raising substantial doubt about its ability to continue as a going concern, with the company relying on its June 2025 ATM agreement, which allows for sales of up to $50 million in stock, and remaining CIRM grant funds to finance future operations, though additional capital will be necessary - The company had approximately $11.6 million in cash and cash equivalents as of June 30, 2025152 - Management believes that current cash and cash equivalents will not be sufficient to fund planned operations over the next twelve months, and there is substantial doubt about the company's ability to continue as a going concern152176 - The company is funding operations through its June 2025 ATM agreement (raised $2.4 million as of Aug 6, 2025), and an $8 million CIRM grant ($4.4 million remaining to be disbursed upon milestone achievement)150151 Quantitative and Qualitative Disclosures About Market Risk The company is a "smaller reporting company" as defined by the Exchange Act and is therefore not required to provide the information for this item - As a 'smaller reporting company,' the company is not required to provide quantitative and qualitative disclosures about market risk166 Controls and Procedures Management concluded that as of June 30, 2025, the company's disclosure controls and procedures were not effective due to a previously identified material weakness in internal control over financial reporting, stemming from the company's small size and lack of adequate segregation of duties, with a remediation plan ongoing - Management concluded that disclosure controls and procedures were not effective as of June 30, 2025167 - The ineffectiveness is due to a material weakness in internal control over financial reporting related to the company's small size and limited personnel, which prevents adequate segregation of duties168 - The company is working to remediate the material weakness by establishing additional points of segregation of duties and upgrading IT controls170 PART II. OTHER INFORMATION Legal Proceedings The company reports that it is not currently aware of any pending legal proceedings that would have a material adverse effect on its business, financial condition, or operating results - The company is not currently a party to any material legal proceedings174 Risk Factors The company states there have been no material changes to its risk factors from its 2024 Annual Report, with the exception of highlighting the risk related to its ability to continue as a 'going concern', which arises from recurring losses and the need to raise additional capital to fund future operations - The company's ability to continue as a going concern is identified as a key risk, as existing cash is not expected to fund operations into the third quarter of 2026, creating substantial doubt about its viability within one year176 Unregistered Sales of Equity Securities and Use of Proceeds During the six months ended June 30, 2025, the company issued a total of 183,531 shares of restricted common stock, valued at a combined $0.3 million, for investor relations services under various marketing agreements, with these issuances exempt from registration under the Securities Act - The company issued shares of restricted common stock for investor relations services in three separate transactions during the first six months of 2025178179180 Other Information During the quarter ended June 30, 2025, none of the company's directors or officers adopted or terminated any Rule 10b5-1 trading plans for the purchase or sale of company securities - No directors or officers adopted or terminated a Rule 10b5-1 trading plan during the second quarter of 2025183 Exhibits This section lists the exhibits filed with the Quarterly Report on Form 10-Q, including the At The Market Offering Agreement, officer certifications (pursuant to Sarbanes-Oxley Act Sections 302 and 906), and Inline XBRL data files - Exhibits filed include the At The Market Offering Agreement with Citizens JMP Securities, LLC, and required certifications by the Principal Executive Officer and Principal Financial Officer185