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Pfizer, Merck Are Boring Again — And That's Exactly Why 2026 Investors Are Circling Back
Benzinga· 2025-12-17 15:14
Core Insights - Pfizer and Merck are experiencing a shift in market perception, with both companies focusing on stability rather than high-growth narratives [1][7] - Pfizer's cautious outlook for 2026 indicates ongoing challenges post-COVID, with expectations for flat-to-low single-digit growth [2][3] - Merck has maintained better performance due to strong oncology cash flows and consistent execution, appealing to investors seeking reliability [4][6] Pfizer Overview - Pfizer's stock is trading below pandemic-era multiples, with a current yield exceeding 6%, making it one of the highest in large-cap pharmaceuticals [3] - The company is prioritizing targeted dealmaking, exemplified by a recent collaboration with Adaptive Biotechnologies valued at up to $890 million, focusing on autoimmune diseases [5][6] - The strategy reflects a balance-sheet-aware approach to pipeline development rather than aggressive expansion [6] Merck Overview - Merck's dividend yield is between 3-4%, attracting investors looking for dependable returns rather than speculative growth [4] - The company's pipeline does not rely on a single breakthrough, as incremental progress and steady oncology performance are sufficient to support its valuation [6] - Merck's strategy mirrors Pfizer's in its focus on maintaining a stable earnings base without significant balance-sheet stress [4][6] Market Implications for 2026 - The market may favor companies that demonstrate consistent execution over those that promise high growth but carry execution risks [7] - Pfizer and Merck's "boring" profiles may become advantageous in a market increasingly wary of volatility and uncertainty [7]
KEYTRUDA® (pembrolizumab) Plus Padcev® (enfortumab vedotin-ejfv) Significantly Improved Event-Free Survival, Overall Survival and Pathologic Complete Response Rates for Cisplatin-Eligible Patients with MIBC When Given Before and After Surgery
Businesswire· 2025-12-17 11:45
Core Insights - Merck announced positive topline results from the Phase 3 KEYNOTE-B15 trial for patients with muscle-invasive bladder cancer (MIBC) eligible for cisplatin-based chemotherapy [1] - The trial evaluated the combination of KEYTRUDA® (pembrolizumab) and Padcev® (enfortumab vedotin-ejfv) as neoadjuvant and adjuvant treatment, showing statistically significant results [1] Company Summary - Merck, known as MSD outside the United States and Canada, is focusing on innovative cancer treatments [1] - The positive results from the KEYNOTE-B15 trial may enhance Merck's position in the oncology market [1] Industry Summary - The trial results contribute to the growing body of evidence supporting immunotherapy and targeted therapy combinations in treating bladder cancer [1] - The findings may influence treatment protocols and patient outcomes in the field of oncology [1]
MRK Gets Positive CHMP Opinion for Expanded Use of Winrevair in PAH
ZACKS· 2025-12-15 15:51
Core Viewpoint - Merck (MRK) received a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) recommending approval for an expanded indication of its pulmonary arterial hypertension (PAH) drug, Winrevair (sotatercept) [1][7]. Group 1: Approval and Study Data - The CHMP recommended the approval of Winrevair in combination with other PAH therapies for adult patients with WHO Functional Class (FC) II, III, and IV, based on data from the phase III ZENITH study [2][5]. - The ZENITH study demonstrated a statistically significant and clinically meaningful 76% reduction in the risk of major morbidity and mortality outcomes when Winrevair was added to background therapy [5][8]. - The final decision from the European Commission regarding the expanded indication is expected in the first quarter of 2026 [2][7]. Group 2: Current Status and Market Performance - Winrevair is currently approved in the EU for treating adults with PAH with WHO FC II to III to improve exercise capacity [3]. - Year-to-date, Merck's shares have increased by 0.9%, while the industry has seen a rally of 15.9% [4]. - Winrevair recorded sales of $976 million in the first nine months of 2025, indicating its potential as a growth driver for Merck [11]. Group 3: Competitive Landscape - Significant competitors in the PAH market include United Therapeutics and Johnson & Johnson, with United Therapeutics' Tyvaso generating sales of $1.41 billion and J&J's PAH franchise recording revenues of $3.25 billion in the first nine months of 2025 [12][13]. - Merck's Winrevair is likely to face stiff competition in the PAH market despite its promising data and sales performance [11].
BioVaxys Strengthens Scientific Team with Addition of Former IMV Vice President of R&D
Thenewswire· 2025-12-15 13:00
Core Insights - BioVaxys Technology Corp. has appointed Dr. Marianne Stanford as Scientific Advisor, bringing extensive experience in vaccine development and immunotherapy [1][4] - Dr. Stanford previously led the R&D at IMV Inc., where she developed the DPX™ vaccine portfolio, demonstrating enhanced efficacy in cancer models through innovative combinations [1][2] - The company focuses on novel immunotherapies using the DPX platform, targeting cancers and infectious diseases, with ongoing clinical trials for multiple products [4] Company Overview - BioVaxys Technology Corp. is a clinical-stage biopharmaceutical company based in British Columbia, Canada, dedicated to developing immunotherapies for various diseases [4] - The DPX platform is designed to generate specific and robust immune responses, with a clinical pipeline that includes MVP-S for advanced cancers and other immunotherapies [4] Dr. Stanford's Background - Dr. Stanford holds a PhD in Microbiology and Immunology and has a strong background in viral immunotherapy and oncology, enhancing her role at BioVaxys [3] - Her previous role as Chief Scientific Officer at Mara Renewables Corp. involved the commercialization of bio-based nutrition products, showcasing her leadership in scientific research [2]
Abeona Therapeutics® Announces Appointment of Mohamad Tabrizi as Chief Business Officer
Globenewswire· 2025-12-15 12:30
Core Viewpoint - Abeona Therapeutics Inc. has appointed Mohamad Tabrizi as Senior Vice President and Chief Business Officer to enhance corporate strategy and business development efforts [1][2]. Group 1: Appointment and Role - Mohamad Tabrizi will lead the company's corporate strategy and business development functions, focusing on driving operational efficiency [1]. - Tabrizi has extensive experience in strategic planning and business development, which the company aims to leverage for optimizing operations and forming value-creating partnerships [2]. Group 2: Professional Background - Tabrizi previously worked in the venture capital sector as a General Partner and Managing Director at Pandect Bioventures and the Berkeley Catalyst Fund, where he led investment activities and operational roles [2]. - He has a strong track record in corporate development and capital markets, having executed 20 transactions at Nektar Therapeutics and led over 40 transactions as a healthcare investment banker, raising more than $5 billion [3]. Group 3: Company Overview - Abeona Therapeutics is a commercial-stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases, including its product ZEVASKYN, the first autologous cell-based gene therapy for treating wounds in patients with recessive dystrophic epidermolysis bullosa [4]. - The company operates a fully integrated cGMP manufacturing facility in Cleveland, Ohio, which is responsible for the commercial production of ZEVASKYN [4].
Why Ditching Schwab U.S. Dividend Equity ETF In the AI Era Is a Mistake
Yahoo Finance· 2025-12-13 16:10
Core Insights - The rise of artificial intelligence (AI) has significantly impacted the stock market, benefiting technology companies and growth-oriented investments while putting pressure on dividend-focused funds like the Schwab U.S. Dividend Equity ETF (SCHD) [2][4] Group 1: ETF Overview - The Schwab U.S. Dividend Equity ETF tracks the Dow Jones U.S. Dividend 100 Index, focusing on high-quality U.S. firms with consistent dividend payments and strong financial ratios [3] - The ETF currently offers a trailing yield of approximately 3.8%, which is higher than the S&P 500's payout, and has a low expense ratio of 0.06% [3] Group 2: Performance Analysis - The SCHD has underperformed during the AI boom, with year-to-date total returns being near flat or slightly positive, while tech-focused funds like the Invesco QQQ Trust have seen stronger gains [7][8] - The ETF's portfolio is heavily weighted towards stable dividend payers in sectors such as energy (19%), consumer discretionary (18%), and healthcare (16%), with limited exposure to high-growth AI leaders [6][8] Group 3: Market Dynamics - The AI surge has concentrated market gains among a few mega-cap tech stocks, which prioritize reinvesting profits into growth rather than paying dividends, thus limiting their representation in SCHD's portfolio [5] - The equity risk premium has approached zero in 2025, indicating potential overvaluation reminiscent of the dot-com era [8]
Can MRK's New Drugs & Pipeline Help Navigate the Looming Keytruda LOE?
ZACKS· 2025-12-12 16:05
Core Viewpoint - Merck is strategically focusing on long-term growth through new product launches and a robust pipeline as its leading drug, Keytruda, is set to lose patent protection in 2028 [1][2]. Pipeline and Product Development - Keytruda, which accounts for over 50% of Merck's pharmaceutical sales, generated $23.3 billion in sales during the first nine months of 2025, reflecting an 8% year-over-year increase [2]. - The company's phase III pipeline has nearly tripled since 2021, with plans to launch around 20 new vaccines and drugs in the coming years, many of which have blockbuster potential [3][11]. - Notable new products include the 21-valent pneumococcal conjugate vaccine, Capvaxive, and the pulmonary arterial hypertension drug, Winrevair, both of which are expected to significantly contribute to revenue post-Keytruda exclusivity [4][11]. Strategic Mergers and Acquisitions - Merck has engaged in substantial M&A activities, including a recent agreement to acquire Cidara Therapeutics for $9.2 billion, which will enhance its portfolio with CD388 for seasonal influenza prevention [7][8]. - Earlier this year, Merck acquired Verona Pharma for $10 billion, adding Ohtuvayre, a novel treatment for chronic obstructive pulmonary disease [8]. Competitive Landscape - Keytruda faces competition from other PD-L1 inhibitors such as Bristol Myers' Opdivo, Roche's Tecentriq, and AstraZeneca's Imfinzi, which are also approved for multiple cancer types [10][12][13]. Financial Performance and Valuation - Year-to-date, Merck's shares have decreased by 0.4%, underperforming the industry average of 13.6% [14]. - The company's price/earnings ratio stands at 11.22, which is lower than the industry average of 16.59 and its 5-year mean of 12.51, indicating a potentially attractive valuation [15]. - The Zacks Consensus Estimate for 2025 earnings per share has slightly increased from $8.94 to $8.98, while the estimate for 2026 has decreased from $9.46 to $8.81 [18].
Merck Receives Positive EU CHMP Opinion for Expanded Use of WINREVAIR™ (sotatercept) in Adults with Pulmonary Arterial Hypertension (PAH, WHO* Group 1 Pulmonary Hypertension)
Businesswire· 2025-12-12 13:45
Core Viewpoint - Merck announced that the European Medicines Agency's Committee for Medicinal Products for Human Use recommended the approval of an expanded indication for WINREVAIR™ (sotatercept) for treating pulmonary arterial hypertension (PAH) in adult patients [1] Group 1: Product Information - WINREVAIR™ (sotatercept) is recommended for use in combination with other PAH therapies [1] - The recommendation is based on the results of the Phase 3 ZENITH study [1] Group 2: Patient Population - The expanded indication targets adult patients with WHO Functional Class (FC) II, III, and IV [1]
MAIA Takes Aim at a $50B Immunotherapy Market with Breakthrough Telomere-Targeting Approach
Globenewswire· 2025-12-10 19:00
Core Viewpoint - The treatment landscape for advanced non-small cell lung cancer (NSCLC) is shifting towards a new class of therapies, specifically telomere-targeting agents, to address the unmet medical needs of patients without actionable mutations and those who are resistant to current therapies [1][4]. Industry Overview - Checkpoint inhibitors (CPIs) dominate the NSCLC treatment market, generating approximately $50 billion in global sales in 2024, with Merck's Keytruda accounting for $29.5 billion of that revenue [3][9]. - The NSCLC market is projected to grow from $34.1 billion to nearly $68.8 billion by 2033, indicating significant commercial opportunities for new therapies [7]. Company Insights - MAIA Biotechnology's ateganosine is positioned as a first-in-class telomere-targeting agent, designed to exploit telomerase activity found in over 80% of human tumors, offering a novel mechanism of action [5][12]. - The U.S. FDA has granted Fast Track Designation to ateganosine for treating NSCLC patients resistant to immunotherapy and chemotherapy, and a Phase 3 trial is set to begin [6]. Market Dynamics - The oncology market is expected to reward innovative therapies that fill existing treatment gaps, particularly in advanced NSCLC, which represents a significant unmet need [8][11]. - A significant portion of CPI sales, over 40%, is derived from NSCLC, highlighting the importance of this segment in the overall oncology market [9].
MRK Stock Trading Above 200- & 50-Day SMA for 2 Months: Time to Buy?
ZACKS· 2025-12-09 17:06
Core Insights - Merck's stock has shown sustained bullish momentum, trading above its 50-day and 200-day simple moving averages since early November [2][8] - The company announced a $9.2 billion acquisition of Cidara Therapeutics, which will enhance its antiviral pipeline [4] - Keytruda remains a significant revenue driver, accounting for over 50% of pharmaceutical sales, with sales reaching $23.3 billion in the first nine months of 2025, an 8% year-over-year increase [6][31] Pipeline and Strategic Developments - Merck's phase III pipeline has nearly tripled since 2021, positioning the company to launch around 20 new vaccines and drugs in the coming years [12] - The acquisition of Verona for $10 billion added Ohtuvayre, a novel treatment for chronic obstructive pulmonary disease, which has multibillion-dollar commercial potential [15] - Merck is also developing a personalized mRNA therapeutic cancer vaccine in collaboration with Moderna, which is currently in pivotal phase III studies [9] Challenges and Concerns - Sales of the Gardasil vaccine have declined by 40% in the first nine months of 2025, primarily due to weak demand in China [16] - Keytruda is set to lose exclusivity in 2028, raising concerns about Merck's reliance on this drug and its ability to diversify its product lineup [19][20] - Competitive pressures are increasing, particularly from dual PD-1/VEGF inhibitors that may challenge Keytruda's market position [20][21] Financial Performance and Valuation - Merck's shares have underperformed the industry and the S&P 500, losing 0.5% year-to-date compared to a 14.1% increase for the industry [22] - The company's price/earnings ratio stands at 11.21, lower than the industry average of 16.68, indicating potential attractiveness from a valuation perspective [26] - Earnings estimates for 2025 have slightly increased, while those for 2026 have declined, reflecting mixed market sentiment [29]