Insider Trading February 18, 2026

Invivyd CFO Disposes of 40,627 Shares as Company Advances VYD2311 Phase 3 Plans

William E. Duke sold roughly $63,350 of stock amid option exercises and a push toward a Phase 3 LIBERTY trial for VYD2311

By Avery Klein IVVD
Invivyd CFO Disposes of 40,627 Shares as Company Advances VYD2311 Phase 3 Plans
IVVD

Invivyd Inc.'s Chief Financial Officer, William E. Duke, executed sales totaling 40,627 common shares on February 17 and 18, 2026, for approximately $63,350. The transactions followed option exercises and RSU conversions on February 15, and come as the company receives FDA feedback on its planned Phase 3 LIBERTY study of VYD2311. H.C. Wainwright has maintained a Buy rating and $10.00 price target, and Invivyd announced a national antibody education campaign with Lindsey Vonn set for spring 2026.

Key Points

  • CFO William E. Duke sold 40,627 shares of Invivyd common stock on February 17 and 18, 2026, totaling approximately $63,350.
  • On February 15, Duke exercised options on 99,000 shares and converted 99,000 Restricted Stock Units to common stock.
  • Invivyd received FDA feedback on its planned Phase 3 LIBERTY trial of VYD2311, which will assess safety and immunologic profile versus mRNA COVID vaccines and evaluate co-administration. H.C. Wainwright reaffirmed a Buy rating and $10.00 price target. The company also announced a national antibody education campaign with Lindsey Vonn launching in spring 2026.

Invivyd, Inc. (NASDAQ: IVVD) reported that its Chief Financial Officer, William E. Duke, sold a total of 40,627 shares of common stock over two days in mid-February 2026 for an aggregate amount of about $63,350.

The share disposals were completed in two tranches. On February 17, Duke sold 19,663 shares at a weighted average price of $1.5396. The following day, February 18, he sold 20,964 shares at a weighted average price of $1.5778. Across the two transactions, the executed prices ranged from $1.505 to $1.595.

Earlier in the week, on February 15, Duke exercised options covering 99,000 shares of common stock and converted 99,000 Restricted Stock Units into common stock. The filings indicate these actions and subsequent sales as related insider transaction activity within a short time frame.


Separately, Invivyd disclosed regulatory and program updates tied to its lead monoclonal antibody candidate, VYD2311. The company has received feedback from the U.S. Food and Drug Administration concerning the design of a planned Phase 3 study, named LIBERTY. That trial is intended to evaluate the safety and immunologic profile of VYD2311 in comparison to commercially available mRNA COVID-19 vaccines, and will also examine effects when VYD2311 is administered alongside an mRNA COVID vaccine. LIBERTY forms a central component of Invivyd's broader REVOLUTION clinical program.

Market analysts have reacted to these program developments. H.C. Wainwright has reiterated a Buy rating on Invivyd and retained a $10.00 price target, citing confidence in the company’s near-term value potential and management’s focus on delivering Phase 3 topline results, which are expected in August.

In a separate outreach effort, Invivyd announced a partnership with Olympic gold medalist Lindsey Vonn to roll out a national educational campaign about antibodies. The campaign is scheduled to begin in spring 2026 and will feature Vonn as a spokesperson. The stated aim is to increase public understanding of the role antibodies play in preventing infectious diseases.


Taken together, the insider sales, the exercise and conversion activity, regulatory feedback on a pivotal Phase 3 trial, analyst affirmation, and a public education partnership underline a period of active corporate and clinical development for Invivyd. The company is proceeding with the LIBERTY trial planning while preparing for results expected later in the year.

Risks

  • Regulatory uncertainty - FDA feedback on the planned Phase 3 LIBERTY trial indicates the study design is under regulatory review, which could affect timelines and requirements for VYD2311 development - impacts the biotech and healthcare sectors.
  • Clinical outcome risk - Phase 3 topline results for VYD2311 are expected in August; the ultimate trial results will materially influence Invivyd’s clinical progress and valuation - impacts biotech investors and clinical-stage therapeutics markets.
  • Perception risk tied to insider sales - The CFO's sale of 40,627 shares and prior exercise/conversion activity may be viewed variably by market participants, potentially affecting investor sentiment in the stock - impacts equity markets and investor perception of small-cap biotech.

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