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Merck’s $3 billion cost-cutting and reinvestment strategy represents a calculated effort to navigate the impending patent expiry of Keytruda in 2028 while preserving long-term value for shareholders. With Keytruda generating $8 billion in sales during Q2 2025 [1], the company faces a critical
as biosimilar competition looms. Merck’s approach combines aggressive operational efficiency, strategic R&D redirection, and lifecycle management to mitigate revenue erosion and diversify its portfolio.Merck’s $3 billion annual savings by 2027 will be fully reinvested into high-growth areas, including oncology, immunology, and cardio-pulmonary therapies [1]. The cost-cutting plan includes a global reduction of 6,000 jobs, primarily in administrative, sales, and R&D roles, alongside real estate optimization and manufacturing streamlining [1]. These measures are not merely defensive but are designed to fund innovation. For instance, $1 billion of the savings will be allocated to a new Delaware biologics center for Keytruda production, while $895 million will expand a Kansas animal health facility [1]. By redirecting resources from slower-growth areas,
aims to accelerate the development of next-generation therapies.A cornerstone of Merck’s strategy is the $10 billion acquisition of
, which added Ohtuvayre—a first-in-class COPD treatment—to its pipeline [1]. This acquisition targets a $10 billion market and provides a near-term revenue catalyst. Simultaneously, Merck is advancing enlicitide decanoate, an oral PCSK9 inhibitor for hyperlipidemia, which demonstrated significant LDL-C reductions in Phase 3 trials [1]. These investments underscore Merck’s focus on expanding beyond oncology, a sector increasingly vulnerable to patent cliffs.To delay biosimilar competition, Merck is prioritizing lifecycle management for Keytruda. The company expedited the approval of a subcutaneous (SC) formulation, expected to launch in 2025 [2]. This reformulation offers greater patient convenience, potentially capturing 30–40% of the market before biosimilars enter [3]. Additionally, Merck has expanded Keytruda’s indications to include neoadjuvant/adjuvant settings for triple-negative breast cancer and head and neck squamous cell carcinoma [1]. These moves reinforce Keytruda’s clinical value and extend its market dominance.
Despite Keytruda’s projected sales decline post-2028, Merck’s 2025 revenue guidance remains robust at $64.3–$65.3 billion [1]. Analysts project non-GAAP EPS of $8.87–$8.97 for 2025, with a Zacks Consensus price target of $145 per share [1]. The company’s cost discipline and reinvestment strategy are critical to maintaining this trajectory. By balancing near-term efficiency with long-term innovation, Merck aims to offset Keytruda’s eventual sunset while capitalizing on emerging therapeutic opportunities.
Merck’s $3 billion reinvestment strategy exemplifies strategic preparedness in a post-patent world. By leveraging cost savings to fund innovation, diversifying its portfolio through acquisitions, and extending Keytruda’s lifecycle, the company is positioning itself to weather the patent expiry storm. While challenges remain—such as declining Gardasil sales in Asia—Merck’s focus on operational efficiency and R&D agility provides a compelling case for long-term value preservation.
**Source:[1] Merck unveils $3B cost-cutting plan [https://www.fiercepharma.com/pharma/merck-joins-big-pharma-cost-cutting-crowd-revealing-plan-save-3b-annually-through-2027][2] Merck Cuts $3 Billion in Costs as Keytruda Reign Nears End [https://www.bloomberg.com/news/articles/2025-07-29/merck-mounts-3-billion-revamp-as-keytruda-price-pressure-looms][3] May 2025: Merck's Scheme to Product Hop Keytruda [https://www.i-mak.org/2025/05/05/may-2025-mercks-scheme-to-product-hop-keytruda/]
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