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Merck Shares Drop on Insider Sale, Investors Await Key FDA Decision

Merck & Co. stock fell 3.5% amid an executive share sale and underperformance versus a broader market rally. Traders are focused on an upcoming FDA ruling for Keytruda's ovarian cancer expansion.

StockTi Editorial · · 2 min read · 1 views
Merck Shares Drop on Insider Sale, Investors Await Key FDA Decision
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AMGN $384.32 +4.49% MRK $121.93 +1.82% XLV $157.71 +1.85%

Shares of Merck & Co. declined 3.5% on Monday, closing at $117.65, as the pharmaceutical giant lagged behind a broader market rebound led by technology stocks. Trading volume reached approximately 16.2 million shares during the session.

Market Context and Sector Pressure

The S&P 500 and Nasdaq Composite ended the day higher, driven by gains in tech shares. However, the healthcare sector within the S&P 500 slipped 0.86%, reflecting a rotation away from defensive names. Merck, along with Amgen, acted as a drag on the Dow Jones Industrial Average's performance for the day.

Insider Transaction Details

A regulatory filing revealed that Jennifer Zachary, Merck's Executive Vice President and General Counsel, exercised stock options and sold 121,573 company shares on February 9. The transaction was executed at a weighted-average price of $119.15. Following the sale, her direct holdings were reduced to about 68,916 shares. Such sales are often related to personal financial planning rather than a commentary on the company's prospects.

Pipeline Focus and Upcoming Catalyst

Investor attention remains fixed on Merck's drug development pipeline, particularly its heavy reliance on the blockbuster cancer immunotherapy Keytruda. The company faces increasing competition for its older products, heightening the need for successful new drug launches and label expansions.

A significant near-term catalyst is approaching. The U.S. Food and Drug Administration is expected to issue a decision by February 20 on Merck's application to expand Keytruda's use. The proposal seeks approval for combining the drug with chemotherapy, with or without bevacizumab, for treating certain patients with platinum-resistant recurrent ovarian cancer. Keytruda is not currently approved for ovarian cancer.

This Prescription Drug User Fee Act (PDUFA) date represents a clear event risk for traders, though regulatory delays remain possible. The outcome could significantly influence market sentiment toward Merck's growth trajectory beyond its flagship product.

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