US Stock Insider Trading | Zevra disclosed 5 insider transactions on February 2

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On February 2, 2026, Zevra (ZVRA) disclosed five insider transactions. Director McFarlane Neil F. sold 91,000 shares on February 2, 2026.

【Recent Insider Transactions】

Disclosure Date Position Name Transaction Date Buy/Sell Quantity Price per Share/USD Total Amount/USD
February 2, 2026 Executive Thompson Rahsaan January 30, 2026 Sell 4,080 8.83 $36,000
February 2, 2026 Executive Quartel Adrian W January 30, 2026 Sell 4,533 8.83 $40,000
February 2, 2026 Executive Sangiovanni Timothy J. January 30, 2026 Sell 1,750 8.82 $15,400
February 2, 2026 Director McFarlane Neil F. February 2, 2026 Sell 91,000 9.38 $853,400
February 2, 2026 Executive Schafer Joshua January 30, 2026 Sell 3,375 8.83 $28,200
January 7, 2026 Shareholder Clifton R. LaDuane December 31, 2025 Sell 48,500 8.96 $434,700
October 10, 2025 Director McFarlane Neil F. October 10, 2025 Sell 19,500 10.82 $211,900
September 16, 2025 Director FAVORITO TAMARA A September 12, 2025 Buy 3,175 7.79 $24,700
September 15, 2025 Director Shih Alvin September 12, 2025 Buy 20,000 7.89 $157,800
August 20, 2025 Director Bode John B August 19, 2025 Buy 5,000 9.17 $45,800

【Company Information】

Zevra Therapeutics, Inc. was incorporated in October 2006 in Iowa and restructured in Delaware in May 2014. The company is a rare disease company that combines science, data, and patient needs to create transformative therapies for diseases with limited or no treatment options. The company’s mission is to bring life-changing therapies to people with rare diseases. With a unique, data-driven development and commercialization strategy, the company is overcoming complex drug development challenges to provide new treatments for the rare disease community. The company has a diversified portfolio of products and candidates, including preclinical development programs, clinical-stage pipelines, and commercial-stage assets. The team has expertise and a proven track record of advancing promising therapies facing complex clinical and regulatory challenges by balancing science and data with patient needs.

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