Merck Completes Acquisition of Terns Pharmaceuticals at $53 per Share
Merck announced the completion of the acquisition of Terns Pharmaceuticals. TERN-701 was recently granted Breakthrough Therapy Designation by the U.S. Food and Drug Administration for the treatment of adults with Philadelphia chromosome-positive chronic myeloid leukemia in the chronic phase without the T315I mutation previously treated with two or more tyrosine kinase inhibitors. The BTD designation for TERN-701 is based on data from the ongoing Phase 1/2 CARDINAL trial. Merck completed the cash tender offer, through a subsidiary, for all the outstanding shares of common stock of Terns at a purchase price of $53.00 per share, without interest and subject to any applicable tax withholding. As of the tender offer expiration at one minute after 11:59 p.m., Eastern Time, on May 4, 2026, 100,091,794 shares of Terns common stock were validly tendered and not validly withdrawn, representing approximately 86.36% of the total number of Terns' issued and outstanding shares of common stock as of such date and time. All such shares have been accepted for payment in accordance with the terms of the tender offer, and Merck, on behalf of its subsidiary, will promptly pay for such shares. Following the completion of the tender offer, Merck completed the acquisition of Terns through a merger of Merck's wholly-owned subsidiary with and into Terns, with Terns being the surviving corporation, in which all shares of Terns common stock issued and outstanding at the effective time of the merger were converted into the right to receive cash equal to the $53.00 offer price per share, without interest and subject to any applicable tax withholding. At the completion of the merger, Terns became a wholly-owned subsidiary of Merck and Terns' common stock will no longer be listed or traded on the Nasdaq Global Select Market. The transaction is expected to be accounted for as an asset acquisition, resulting in a charge to research and development expense of approximately $5.8B or approximately $2.35 per share, included in both second quarter and full year 2026 GAAP and non-GAAP results. Additionally, GAAP and non-GAAP EPS are expected to be negatively impacted by approximately $0.12 per share in 2026, representing costs associated with advancing TERN-701 and costs of financing.
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- Eligibility Criteria: The newly approved label stipulates that eligible children must have completed a primary pneumococcal vaccination series and have at least one chronic medical condition, ensuring the vaccine's effectiveness and safety for high-risk groups.
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- Strategic Implications: This approval not only broadens Capvaxive's market potential but also lays the groundwork for Merck's ongoing innovation and development in the vaccine sector, expected to boost overall company performance and shareholder returns.
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- Strategic Significance: This approval not only showcases Merck's commitment to public health but also provides a new preventive measure for children and adolescents, further solidifying the company's leadership position in the vaccine market.
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- Stock Performance: As of midday Tuesday, MRK's stock is down approximately 0.7%, indicating a cautious market sentiment towards the pharmaceutical sector, particularly when compared to competitors Eli Lilly and Johnson & Johnson.
- Industry Comparison: Eli Lilly and Johnson & Johnson are down about 0.1% and 1.3%, respectively, highlighting the overall pressure faced by the pharmaceutical industry, which could impact MRK's market performance and investor confidence.
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- Analyst Opinions: Analysts' views on MRK align with market sentiment, reflecting a cautious outlook on the company's future growth, which may influence investor decisions and market liquidity.










