Weight Watchers Introduces Eli Lilly's New Oral GLP-1 Foundayo® via LillyDirect
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Apr 09 2026
0mins
Source: moomoo
Product Launch: Weight Watchers has launched a new oral GLP-1 medication called Dayo® through its subsidiary, LILLY.
Availability: The new medication is available directly through the LILLY platform, expanding Weight Watchers' offerings in weight management solutions.
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Analyst Views on LLY
Wall Street analysts forecast LLY stock price to rise
20 Analyst Rating
18 Buy
2 Hold
0 Sell
Strong Buy
Current: 1126.800
Low
950.00
Averages
1192
High
1500
Current: 1126.800
Low
950.00
Averages
1192
High
1500
About LLY
Eli Lilly and Company is a medicine company, which discovers, develops, manufactures, and market products in a single business segment called human pharmaceutical products. The Company manufacture and distribute its products through facilities in the United States, including Puerto Rico, and in Europe and Asia. The Company’s products are sold in approximately 90 countries. Its Cardiometabolic Health products Basaglar; Humalog, Humalog Mix 75/25, Humalog U-100, Humalog U-200, Humalog Mix 50/50, insulin lispro, and others; Humulin, Humulin 70/30, and others; Jardiance; Mounjaro; Trulicity; Zepbound, and others. Its oncology products include Cyramza, Erbitux, Tyvyt, Verzenio, Retevmo, Jaypirca, and others. Its immunology products include Ebglyss, Olumiant, Omvoh, and Taltz. Its neuroscience products include Emgality and Kisunla. Its LillyDirect, a direct-to-patient digital health care platform, provides delivery of select Lilly medicines dispensed by third-party pharmacies to patients.
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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- Clinical Trial Results: Eli Lilly's targeted cancer therapy Retevmo demonstrated an 83% reduction in the risk of recurrence or death in early-stage RET fusion-positive non-small cell lung cancer patients, a significant finding that could influence treatment practices.
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- Tech Stock Performance: Nvidia and Tesla, among five tech giants nearing buy points, indicate sustained market interest in high-tech stocks, potentially attracting more investors to focus on these companies' growth potential.
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See More
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- Market Leaders: Nvidia and Tesla, among five tech giants nearing buy points, indicate sustained investor interest in tech stocks, which could drive their share prices higher in the short term.
- Improved Investor Sentiment: Trump's policy changes may enhance market sentiment towards energy stocks, particularly against the backdrop of a global economic recovery, prompting investors to reassess the investment value of the energy sector.
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- Analyst Target Upgrades: Bank of America nearly doubled its price target for Micron from $500 to $950, while UBS raised its target from $535 to $1,625, indicating strong market confidence in Micron's growth potential, which could drive further stock price increases.
- Strategic Customer Agreement: Micron signed its first long-term supply agreement with a strategic customer for five years, which helps it stand out from the traditional boom-bust cycles of the semiconductor industry, enhancing its market stability and long-term revenue outlook.
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See More
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- Future Market Outlook: UBS strategists expect the S&P 500 to rise further in the medium term, targeting 7,900 points, emphasizing that market leadership will broaden beyond megacaps, and recommending diversification into global healthcare, industrials, and infrastructure to navigate market volatility.
See More
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- Clinical Trial Results: Eli Lilly's Retevmo demonstrated significant efficacy in the Phase 3 LIBRETTO-432 trial, achieving a statistically significant 83% reduction in the risk of disease recurrence or death, providing a new treatment option for early-stage RET fusion-positive NSCLC patients.
- Survival Rate Improvement: At a median follow-up of 24 months, the 24-month EFS rate was 92% for the Retevmo group compared to 61% for placebo, indicating Retevmo's potential to improve patient survival rates and possibly change treatment standards.
- Safety Profile: The safety profile of Retevmo was consistent with prior trials, with 17% experiencing elevated ALT and 19% elevated AST, but these adverse events were manageable with dose modifications, indicating good tolerability in clinical settings.
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See More
