Merck Rallies 32% After $70B Next-Gen Drug Forecast Despite Keytruda, Gardasil Headwinds
Merck's stock has rallied over 32% in three months, including a 10% January surge after management projected $70 billion in next-generation drug revenues by the mid-2030s. Analysts stay bearish, citing Keytruda's impending loss of exclusivity, double-digit Gardasil declines and softer Q3 pharma growth as Keytruda sales cooled.
1. Merck’s 32% Rally Fails to Shift Bearish Consensus
Merck shares have climbed more than 32% over the past three months, yet twelve of fifteen Wall Street analysts maintain sell or underperform ratings. Consensus 2026 earnings estimates have been trimmed by an average of 8% since October, reflecting concerns that patent expirations for Keytruda in 2028 will erode margins. Meanwhile, HPV vaccine Gardasil volumes declined roughly 12% year-over-year in Q3 as emerging competitors capture share. With free cash flow growth slowing to low single digits, investors remain cautious despite the recent uptick.
2. Post-January Guidance Spurt Sparks ‘Trap’ Warning
On January 12, Merck management stunned investors by upping its long-term pipeline target to $70 billion in annual revenue by the mid-2030s, up from prior guidance of $60 billion. That confidence injected a 10% month-to-month stock surge, but skeptics note that only $30 billion is earmarked for cardiometabolic therapies, with respiratory and infectious disease programs accounting for $20 billion apiece. Given typical mid-stage compound attrition rates of 60%, some strategists warn the lofty target may be difficult to achieve and could leave the current recovery overstated.
3. Keytruda’s Q4 Upside Under Scrutiny
Keytruda still represents over 50% of Merck’s pharmaceutical revenue, yet Q3 oncology sales grew just 5% year-over-year to $5.4 billion, a slowdown from 12% growth in the first half. Investors are now focused on whether the upcoming Q4 release can reverse this trend, with consensus models forecasting a moderate acceleration to 7% growth. Merck has flagged multiple new indication filings in melanoma and lung cancer scheduled for submission by mid-year, which could provide a catalyst if approved on schedule.