OPKO Health(OPK) - 2025 Q1 - Quarterly Report

Revenue Performance - Total revenues for the three months ended March 31, 2025, were $149.95 million, a decrease of 14% compared to $173.69 million for the same period in 2024[238]. - Revenue from services decreased by approximately $24.1 million, or 19%, primarily due to the absence of revenue from divested BioReference lab operations and lower clinical test volumes[239]. - Revenue from products for Q1 2025 decreased by $3.2 million or 8.4% to $34.8 million compared to Q1 2024, primarily due to unfavorable foreign exchange fluctuations and a reduction in Rayaldee sales[245]. - Revenue from the transfer of intellectual property increased by $3.5 million to $12.3 million in Q1 2025, driven by $7.0 million recognized under the BARDA Contract[246]. - Total revenues for Q1 2025 were $47.1 million, a slight increase of 1% compared to $46.8 million in Q1 2024[245]. Financial Loss and Expenses - The company recorded a loss from operations of $67.17 million for the three months ended March 31, 2025, an improvement of 6% compared to a loss of $71.47 million in the same period of 2024[238]. - Research and development expenses increased by 41% to $30.84 million for the three months ended March 31, 2025, compared to $21.94 million in 2024[238]. - Research and development expenses rose by 42.3% to $30.2 million in Q1 2025, primarily due to increased expenses at ModeX and growth in BARDA collaboration[249]. - Selling, general and administrative expenses decreased by 15.5% to $12.7 million in Q1 2025, attributed to lower employee-related expenses[248]. Cash and Investments - The company had cash, cash equivalents, and restricted cash of approximately $449.7 million as of March 31, 2025[260]. - Cash, cash equivalents, and restricted cash amounted to $449.7 million as of March 31, 2025[287]. - The weighted average interest rate for cash, cash equivalents, and restricted cash was approximately 6.2% for the three months ended March 31, 2025[287]. - The principal outstanding balance under Chilean and Spanish lines of credit was $10.7 million at a weighted average interest rate of approximately 5.5%[287]. - The company aims to preserve principal while maximizing yields without significantly increasing risk through investments in high-quality debt instruments[289]. - Investments are maintained at an average maturity of generally less than three months to minimize exposure to adverse shifts in interest rates[289]. Stock and Shareholder Actions - The company announced a stock repurchase program increase of $100 million, bringing the total capacity to $200 million, with $40.2 million spent on repurchasing 25,825,785 shares at an average price of $1.56[230]. - The company announced a $100 million increase to its stock repurchase program, bringing the total capacity to $200 million[261]. Collaborations and Agreements - The company entered into a collaboration agreement with Entera Bio Ltd. to develop an oral dual agonist GLP-1/glucagon peptide for obesity and metabolic disorders, with a 60% ownership interest in the program[232][233]. - The company is expected to receive up to $225 million from Labcorp for the sale of BioReference's oncology assets, including $192.5 million in cash at closing[235]. - The company entered into an agreement to acquire BioReference's oncology and related clinical testing services assets for up to $225 million, expected to close in the second half of 2025[263]. - Under the Merck Agreement, ModeX received an initial payment of $50.0 million and is eligible for up to an additional $860.0 million upon achieving certain milestones, including a $12.5 million milestone payment triggered by the dosing of the first participant in a Phase 1 study[271]. - The company has received or is eligible for up to $275.0 million under the Restated Pfizer Agreement, including $90 million triggered by FDA approval in the U.S. and $85 million from the commencement of sales of NGENLA in Europe and Japan[271]. Regulatory Approvals and Product Development - The company has secured regulatory approvals for Somatrogon (hGH-CTP) in over 50 markets, including the U.S. and EU, and is marketed under the brand name NGENLA®[226]. - ModeX entered into a BARDA Amendment in September 2024, increasing funding by $26.9 million for the development of a next-generation MSTAR multispecific antibody, raising the total BARDA Contract value to $110.0 million, with a potential value of $205.0 million if all options are exercised[267]. Foreign Currency and Risk Management - Approximately 22.3% of the company's revenue for the three months ended March 31, 2025, was denominated in currencies other than the U.S. Dollar, compared to 21.5% in the same period of 2024[236]. - The company held 60 open foreign exchange forward contracts as of March 31, 2025, to mitigate foreign currency transaction risk[237]. - Gross accumulated currency translation adjustments totaled $41.6 million at March 31, 2025, down from $52.7 million at December 31, 2024[285]. Debt and Obligations - The total contractual obligations due by period as of March 31, 2025, amount to $580.9 million, with $70.8 million due in the remaining nine months of 2025[274]. - The company has a total of $250 million in 2044 Notes secured by profit share payments from Pfizer, maturing in July 2044, with interest-only payments required for the first four years[269]. Accounting and Financial Standards - ModeX is currently evaluating the potential impact of new accounting standards issued by the FASB, including ASU 2024-03 and ASU 2023-09, which will affect future financial disclosures[276][277].