
Report Overview and Business Highlights First Quarter 2025 Highlights XOMA Royalty reported significant Q1 2025 pipeline advancements, including MAA submission for tovorafenib and Phase 3 initiation, alongside $18.0 million in cash receipts - Key pipeline advancements include EMA acceptance of the MAA for tovorafenib and Takeda's initiation of a Phase 3 trial for mezagitamab2 - The company acquired an economic interest in Castle Creek's D-Fi (FCX-007) and divested all unpartnered assets from the Kinnate acquisition2 Q1 2025 Cash Receipts | Category | Amount | | :--- | :--- | | Total Cash Receipts | $18.0 million | | Royalty Receipts | $13.4 million | - The CEO emphasized commitment to generating shareholder value via prudent cash deployment, strict expense control, and opportunistic share repurchases, noting a tangible path to sustained cash flow3 Portfolio Developments Royalty and Milestone Acquisitions XOMA expanded its portfolio by acquiring a royalty interest in D-Fi (FCX-007), a Phase 3 asset for DEB, contributing $5 million to a $75 million syndicated financing - XOMA acquired a royalty interest in the Phase 3 asset D-Fi (FCX-007) for dystrophic epidermolysis bullosa (DEB), which holds FDA Orphan Drug and Fast Track designations4 - The company contributed $5 million to a $75 million syndicated royalty financing transaction with Castle Creek Biosciences for the D-Fi asset4 Partner Updates & Milestone Achievements Significant partner progress generated milestone revenue, including Rezolute's Breakthrough Therapy Designations for ersodetug, Day One's MAA filing for tovorafenib ($4.0M milestone), and Takeda's Phase 3 initiation for mezagitamab ($3.0M milestone) - Rezolute received FDA Breakthrough Therapy Designation for ersodetug for two indications, with sunRIZE Phase 3 study enrollment expected to complete in May 2025 and topline data in December 20256 - Day One Biopharmaceuticals' partner Ipsen's MAA filing for tovorafenib with the EMA triggered a $4.0 million milestone payment to XOMA6 - Takeda's dosing of the first patient in a Phase 3 trial for mezagitamab triggered a $3.0 million milestone payment (net) to XOMA in Q27 - XOMA made a final $6 million milestone payment to Affitech Research AS for VABYSMO® achieving specific sales thresholds6 Anticipated 2025 Events of Note XOMA anticipates key 2025 catalysts including a European regulatory decision for Day One's tovorafenib, Rezolute's ersodetug Phase 3 topline data, and Gossamer/Chiesi's PROSERA study results - An EMA decision is expected regarding the MAA for tovorafenib for pediatric low-grade glioma (pLGG)7 - Topline data from the sunRIZE Phase 3 trial of ersodetug are expected in December 20257 - Topline results from the Phase 3 PROSERA study in pulmonary arterial hypertension (PAH) are expected7 - Sildenafil Cream is anticipated to be available via prescription in Q4 2025 under Section 503B of the FDCA7 Financial Results First Quarter 2025 Financial Performance XOMA reported Q1 2025 total income and revenues of $15.9 million, up from $1.5 million in Q1 2024, achieving a net income of $2.4 million from a prior-year loss Q1 2025 vs Q1 2024 Financial Summary | Financial Metric | Q1 2025 | Q1 2024 | Change | | :--- | :--- | :--- | :--- | | Total Income & Revenues | $15.9M | $1.5M | +$14.4M | | R&D Expenses | $1.3M | $33K | +$1.27M | | G&A Expenses | $8.1M | $8.5M | -$0.4M | | Net Income (Loss) | $2.4M | ($8.6M) | +$11.0M | - Revenue increase was driven by income from VABYSMO®, a $4.0 million milestone from Day One/Ipsen, a $4.0 million payment from Takeda, and $1.5 million in estimated royalties for OJEMDA™8 - Increased R&D expenses were mainly due to a $1.0 million pass-through licensing fee related to the Takeda milestone and clinical trial costs for KIN-32489 Cash Position and Capital Allocation As of March 31, 2025, XOMA held $95.0 million in cash, received $18.0 million in Q1 cash receipts, and strategically deployed capital for new assets, share repurchases, and dividends - Ended Q1 2025 with $95.0 million in cash and cash equivalents (including $4.8 million in restricted cash), compared to $106.4 million at year-end 202415 - Total cash receipts for Q1 2025 were $18.0 million, comprising $13.4 million in royalties/commercial payments and $4.6 million in milestones/fees15 - Key uses of cash in Q1 2025 included $5.0 million for a new asset acquisition, $0.5 million to repurchase 25,828 shares of common stock, and $1.4 million for preferred stock dividends15 Consolidated Financial Statements Condensed Consolidated Statements of Operations For Q1 2025, XOMA reported total revenues of $15.9 million and a net income of $2.4 million, a significant improvement from Q1 2024's $1.5 million revenue and $8.6 million net loss Condensed Consolidated Statements of Operations (in thousands, except per share amounts) | | Three Months Ended March 31, | | | :--- | :--- | :--- | | | 2025 | 2024 | | Total income and revenues | $15,912 | $1,490 | | Total operating expenses | $9,983 | $8,494 | | Income (Loss) from operations | $5,929 | ($7,004) | | Interest expense | ($3,467) | ($3,551) | | Net income (loss) | $2,367 | ($8,595) | | Basic net income (loss) per share | $0.06 | ($0.86) | | Diluted net income (loss) per share | $0.06 | ($0.86) | Condensed Consolidated Balance Sheets As of March 31, 2025, XOMA's total assets were $212.8 million (down from $221.3 million), with total liabilities decreasing to $128.1 million and stockholders' equity increasing to $84.6 million Condensed Consolidated Balance Sheets (in thousands) | | March 31, 2025 | December 31, 2024 | | :--- | :--- | :--- | | ASSETS | | | | Cash and cash equivalents | $90,265 | $101,654 | | Total current assets | $113,225 | $125,604 | | Total assets | $212,750 | $221,277 | | LIABILITIES AND STOCKHOLDERS' EQUITY | | | | Total current liabilities | $20,434 | $24,374 | | Long-term debt | $99,934 | $106,875 | | Total liabilities | $128,121 | $139,356 | | Total stockholders' equity | $84,629 | $81,921 | | Total liabilities and stockholders' equity | $212,750 | $221,277 | Condensed Consolidated Statements of Cash Flows In Q1 2025, XOMA generated $2.2 million cash from operations, used $6.7 million in investing and $6.9 million in financing, resulting in an $11.4 million net cash decrease and a $95.0 million period-end balance Condensed Consolidated Statements of Cash Flows (in thousands) | | Three Months Ended March 31, | | | :--- | :--- | :--- | | | 2025 | 2024 | | Net cash provided by (used in) operating activities | $2,198 | ($4,947) | | Net cash used in investing activities | ($6,693) | ($7,246) | | Net cash used in financing activities | ($6,894) | ($4,956) | | Net decrease in cash, cash equivalents and restricted cash | ($11,389) | ($17,149) | | Cash, cash equivalents and restricted cash at beginning of period | $106,416 | $159,550 | | Cash, cash equivalents and restricted cash at end of period | $95,027 | $142,401 | Company Information and Disclosures About XOMA Royalty Corporation XOMA Royalty operates as a biotechnology royalty aggregator, acquiring future economic rights from therapeutic candidates to provide non-dilutive, non-recourse funding to partners - XOMA's business model involves acquiring future economics, including milestones and royalties, from therapeutic candidates of pharmaceutical or biotech companies16 - This model provides selling partners with non-dilutive, non-recourse funding for their corporate purposes16 Forward-Looking Statements This section provides a standard safe harbor disclaimer, cautioning that forward-looking statements regarding future events are subject to significant biotech industry risks and uncertainties, including development failures and regulatory approvals - The press release contains forward-looking statements regarding the timing and amount of potential payments, regulatory events, and overall portfolio potential17 - These statements are not guarantees of performance and are subject to risks, including licensees' ability to fund development, product market viability, and regulatory approval uncertainty1718