Risk Factors Update Summary
- Added risks related to reputation and prospects, including the introduction of new products and indications.
- Added risks related to intellectual property, including challenges from generic pharmaceutical companies and potential patent infringements.
- New regulations with short notice may hinder business objectives, be costly, and carry penalties.
- Increased the percentage of total revenue from key products, with Trulicity and Mounjaro showing significant changes.
- Noted the challenges in drug discovery and development, emphasizing the high rate of failure.
- Highlighted the risks associated with the use of artificial intelligence and emerging technologies in operations.
- Regulatory oversight may be particularly unpredictable, leading to additional costs, uncertainties, and risks.
- Highlighted the importance of maintaining a continuous flow of successful new products and indications.
- Addressed uncertainties in drug approval processes across markets and agencies, leading to delays in product launches.
- Emphasis on sustainability, brand, and reputation protection to avoid negative impacts and enforcement actions.
Full Text Changes in Most Recent 10-K
Intended use: review the highlighted statements. These are additions to the risk factors disclosure in the most recent 10-K filing compared to the previous 10-K filing. Deleted and moved text is less important and is shown for context.
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