Financial Data and Key Metrics Changes - Adjusted earnings per share (EPS) for the second quarter was $2.97, exceeding guidance by $0.11 [5][34] - Total net revenues reached $15.4 billion, surpassing expectations by over $400 million, reflecting a 6.5% operational growth [6][34] - Full-year revenue guidance raised to $60.5 billion, an increase of $800 million, with a total increase of $1.5 billion since the start of the year [6][35] - Adjusted EPS guidance for the full year increased by $0.21, now expected between $11.88 and $12.08 [7][35] Business Line Data and Key Metrics Changes - Immunology revenues exceeded $7.6 billion, with SKYRIZI global sales at $4.4 billion, up 61.8% operationally [10][11] - RINVOQ global sales reached $2 billion, reflecting a 41.2% operational growth [12][13] - Neuroscience revenues were approximately $2.7 billion, up 24% operationally, driven by Vraylar and UBRELVY [19][20] - Oncology revenues were nearly $1.7 billion, with IMBRUVICA sales down 9.5% and VENCLEXTA sales up 8.3% [15][16] - Aesthetics revenues were nearly $1.3 billion, down 8% operationally, impacted by economic challenges [17][18] Market Data and Key Metrics Changes - SKYRIZI continues to gain market share in psoriatic disease, with leadership in psoriasis therapy lines [10][11] - RINVOQ is capturing significant patient share in IBD, with strong uptake in ulcerative colitis and Crohn's disease [12][13] - HUMIRA sales declined to over $1.1 billion, down 58.2% due to biosimilar competition [14] - The aesthetics market is underperforming historical levels, with economic challenges affecting consumer sentiment [18][19] Company Strategy and Development Direction - The company is focused on advancing its pipeline and strategic transactions to support long-term growth [5][9] - Recent acquisitions include Gubra for obesity treatment and KapStan Therapeutics for CAR T platform [8][9] - The company aims to enhance its immunology pipeline with innovative therapies and technologies [25][26] Management's Comments on Operating Environment and Future Outlook - Management expressed confidence in the strong outlook for 2025 and beyond, supported by robust performance across key products [10][38] - The company is well-positioned to navigate economic challenges and capitalize on growth opportunities in various therapeutic areas [19][38] Other Important Information - The company has executed over 30 business development transactions since the beginning of the previous year [8] - Regulatory submissions for new therapies are anticipated, including RINVOQ for alopecia areata and vitiligo [24][25] Q&A Session Summary Question: Impact of Stellara biosimilar on SKYRIZI and RINVOQ - Management noted that while there may be some impact, the core momentum for SKYRIZI and RINVOQ is driven by strong data and physician connections [41][42] Question: Confidence in SKYRIZI and RINVOQ long-term guidance - Management indicated that they are tracking well against long-term guidance and will update it at the appropriate time [47][48] Question: Leveraging global aesthetics footprint for obesity drugs - The company sees a strong opportunity to integrate obesity treatments into its aesthetics practices, capitalizing on existing patient flow [66][68] Question: Status of anti-amyloid monoclonal antibody - The company is evaluating the potential for a registrational trial based on imaging as an endpoint, but specific details were not disclosed [94]

Core Viewpoint - Regeneron Pharmaceuticals is expected to report first-quarter 2025 results on April 29, 2025, with revenue estimates at $3.25 billion and earnings at $8.76 per share. The company has a mixed earnings surprise history, with an average surprise of 3.23% over the last four quarters [1][2]. Financial Performance - The Earnings Surprise Prediction Model indicates a negative Earnings ESP of -0.94%, suggesting a lower likelihood of an earnings beat this quarter [3]. - The Zacks Rank for Regeneron is currently 4 (Sell), indicating a bearish outlook [3]. Product Sales Overview - Eylea, Regeneron's leading drug, is facing sales pressure due to competition from Vabysmo, with expected sales in the U.S. pegged at $1.2 billion for the first quarter [4][5][6]. - The introduction of Eylea HD is anticipated to have positively impacted total Eylea franchise sales due to strong demand [6]. - Dupixent is another significant revenue driver, with sales estimates at $3.7 billion, bolstered by strong prescription trends and recent label expansions [7][8]. - Libtayo's sales are projected at $346 million, driven by increased demand in non-melanoma skin indications and lung cancer treatments [10]. Regulatory and Pipeline Updates - Regeneron received European Commission approval for odronextamab, enhancing its oncology portfolio [11]. - The FDA approved a label expansion for Dupixent, while a complete response letter was issued regarding the extended dosing intervals for Eylea HD [14][15][16]. - The FDA accepted a supplemental biologics license application for Eylea HD, with a target action date set for August 19, 2025 [17]. Shareholder Returns - In February 2025, Regeneron initiated a quarterly cash dividend program at $0.88 per share and authorized a $3.0 billion share repurchase program, totaling approximately $4.5 billion [13]. Market Performance - Regeneron's shares have declined by 21.1% year-to-date, compared to a 7.8% decline in the industry [18].