Ex-Dividend Alert: Gilead Sciences, Merck, and Horace Mann Educators
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Dec 11 2025
0mins
Source: NASDAQ.COM
Upcoming Ex-Dividend Dates: Gilead Sciences Inc (GILD), Merck & Co Inc (MRK), and Horace Mann Educators Corp. (HMN) will trade ex-dividend on 12/15/25, with respective dividends of $0.79, $0.85, and $0.35 scheduled for payment on 12/30/25, 1/8/26, and 12/31/25.
Expected Stock Price Adjustments: Following the ex-dividend date, GILD shares are expected to open 0.65% lower, MRK by 0.87%, and HMN by 0.78%, based on their recent stock prices.
Dividend Yield Estimates: The estimated annualized yields for the upcoming dividends are 2.60% for Gilead, 3.48% for Merck, and 3.11% for Horace Mann, reflecting their historical dividend stability.
Current Trading Performance: As of Thursday trading, shares of Gilead Sciences, Merck, and Horace Mann are up approximately 1.7%, 0.8%, and 1.4%, respectively.
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Analyst Views on GILD
Wall Street analysts forecast GILD stock price to fall over the next 12 months. According to Wall Street analysts, the average 1-year price target for GILD is 137.88 USD with a low forecast of 105.00 USD and a high forecast of 154.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
19 Analyst Rating
16 Buy
3 Hold
0 Sell
Strong Buy
Current: 149.370
Low
105.00
Averages
137.88
High
154.00
Current: 149.370
Low
105.00
Averages
137.88
High
154.00
About GILD
Gilead Sciences, Inc. is a biopharmaceutical company. It is engaged in advancing medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis, COVID-19, cancer, and inflammation. It is focused on discovering, developing, and delivering medicines to address unmet medical needs in virology, oncology, and other therapeutic areas. Its portfolio of marketed products includes Biktarvy, Genvoya, Descovy, Complera/Eviplera, Symtuza, Truvada, Stribild, Sunlenca, Epclusa, Vemlidy, Harvoni, Viread, Livdelzi, Veklury, Yescarta, Tecartus, Trodelvy, AmBisome, and Letairis. Its product candidates include Bulevirtide, Lenacapavir, Axicabtagene ciloleucel, Sacituzumab govitecan-hziy, and others. It also develops the HB-400 program and the HB-500 program. It develops therapies that are intended to provide functional cures for hepatitis B virus and human immunodeficiency virus-1. It has a cancer program, namely TREX1. It operates in more than 35 countries worldwide.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- FDA Approval Update: Gilead's Kite unit announced that the FDA has approved a label update for its CAR-T therapy Yescarta, removing usage limitations for patients with relapsed or refractory primary central nervous system lymphoma, significantly broadening the therapy's applicability.
- First Unrestricted Therapy: Yescarta becomes the first CAR-T therapy for relapsed or refractory large B-cell lymphoma to have these restrictions lifted, which will help more patients access treatment and enhance the company's competitive position in this field.
- Clinical Data Support: The FDA's decision is backed by favorable safety data from a Phase 1 study that tested the autologous T cell immunotherapy in lymphoma patients, including those with relapsed or refractory primary central nervous system lymphoma, demonstrating good safety and efficacy.
- Market Potential Boost: This label update not only opens new market opportunities for Gilead but may also drive sales growth for Yescarta, further solidifying its leadership position in the CAR-T therapy market.
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- Positive Market Reaction: This FDA approval is expected to boost investor confidence, potentially leading to a positive impact on Gilead's stock price, reflecting market recognition of its innovative treatment solutions.
- Strategic Implications: The approval not only strengthens Kite's position in the highly competitive biopharmaceutical market but also opens up new revenue streams for the company, further solidifying its leadership in the cell therapy sector.
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- Reinforced Safety Data: The updated label highlights the safety profile of Yescarta in eligible patients, with 85% experiencing neurologic toxicities and 31% reporting Grade 3 toxicities, indicating the need for careful assessment of treatment risks versus benefits.
- Addressing Clinical Needs: With a five-year survival rate of only 30% for primary CNS lymphoma, the FDA's decision provides new treatment options for this underserved patient population, potentially improving survival outcomes.
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See More
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- Safety Data Emphasis: The updated label highlights Yescarta's robust safety profile in patients with relapsed or refractory CNS lymphoma, where 85% experienced neurologic toxicities, yet the FDA deemed the risks manageable, underscoring Yescarta's unique position in this treatment landscape.
- Urgent Market Need: With a five-year survival rate of only 30% for primary CNS lymphoma and over half of patients relapsing after initial treatment, the FDA's decision provides much-needed new treatment options, addressing the urgent demand for effective therapies in this underserved market.
- Clinical Study Results: In the Phase 1 study, 18 patients were enrolled, with 13 having relapsed or refractory CNS lymphoma, demonstrating Yescarta's safety and efficacy, thus providing clinicians with critical evidence to support its clinical application and broaden patient access.
See More
