Insider Trading February 11, 2026

Merck Executive Vice President Sells $1.2M in Stock Following FDA Approval and Analyst Revisions

Dean Y. Li disposed of 10,235 Merck shares; analysts respond to FDA approvals for Keytruda and adjustments to guidance

By Nina Shah MRK
Merck Executive Vice President Sells $1.2M in Stock Following FDA Approval and Analyst Revisions
MRK

Dean Y. Li, Executive Vice President at Merck & Co (MRK), sold 10,235 shares on February 10, 2026, for about $1.2 million at a weighted average price of $117.5226. After the transaction, Li retains direct ownership of 92,035.05 shares. Separately, Merck secured FDA approval for Keytruda and Keytruda Qlex in a subset of ovarian cancer patients, and several analysts updated price targets and ratings in light of the company’s product and pipeline developments.

Key Points

  • Dean Y. Li sold 10,235 Merck shares on February 10, 2026, for about $1.2 million at a weighted average price of $117.5226; sale prices ranged from $117.5200 to $117.5550.
  • After the sale, Li directly owns 92,035.05 shares of Merck & Co.
  • Merck received FDA approval for Keytruda and Keytruda Qlex for PD-L1 expressing, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal carcinoma; several analysts adjusted price targets in response to the company's product and pipeline developments.

Merck & Co Executive Vice President Dean Y. Li sold 10,235 shares of the company's common stock on February 10, 2026, realizing proceeds of roughly $1.2 million. The sale carried a weighted average price of $117.5226, with the recorded sale prices spanning from $117.5200 to $117.5550.

Following the transaction, Li's direct stake in Merck amounts to 92,035.05 shares.

In a separate corporate development, Merck received U.S. Food and Drug Administration approval for its immunotherapy treatments Keytruda and Keytruda Qlex for use in a defined group of ovarian cancer patients. The approval covers patients with platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal carcinoma who express PD-L1.

Analyst reactions to Merck's recent regulatory and corporate developments have been mixed but generally showed confidence from several firms. Guggenheim raised its price target for Merck to $140, pointing to long-term growth drivers even as it noted the company's 2026 revenue guidance fell short of some expectations. BMO Capital increased its target to $135, attributing the change in part to potential extensions of Keytruda's patent protection. Wells Fargo also moved its target to $135, kept an Overweight rating, and cited confidence in Merck's new product launches and late-stage pipeline. Bernstein set a $100 price target, highlighting optimism around the pipeline and new product introductions while noting a company-provided "soft-guide."

Taken together, the insider sale and the cluster of analyst updates arrive against the backdrop of a significant regulatory milestone for Keytruda-related treatments. Some analysts have raised their valuation targets and reiterated confidence in Merck's future growth, while others have tempered expectations in light of the company's guidance.


Key takeaway: An executive-level sale of Merck stock occurred alongside FDA approvals and a range of analyst target adjustments, reflecting both regulatory progress and varied market interpretation of Merck's near-term guidance.

  • Ownership change: Dean Y. Li sold 10,235 shares and now directly holds 92,035.05 shares.
  • Regulatory milestone: FDA approval granted for Keytruda and Keytruda Qlex for specific PD-L1 expressing ovarian cancers.
  • Analyst moves: Price targets were revised to $140 (Guggenheim), $135 (BMO Capital and Wells Fargo), and $100 (Bernstein), reflecting differing views on Merck's guidance and pipeline prospects.
  • Sector impact: Developments primarily affect the pharmaceutical and healthcare sectors, with implications for equity valuations in large-cap biotech and drug developers.

Risks

  • Company guidance for 2026 revenue was described as falling short of expectations, introducing near-term uncertainty for Merck's financial outlook; this affects equity valuation in the pharmaceutical sector.
  • Analyst opinions vary, as reflected by divergent price targets, which signals uncertainty among investors about the pace and magnitude of Merck's future growth driven by new product launches and the late-stage pipeline.
  • While some analysts cited potential extensions of Keytruda's patent protection, patent outcomes and their timing remain uncertain and could influence long-term revenue assumptions for the company.

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