Eli Lilly stands poised to revolutionize obesity treatment with its experimental oral medication Orforglipron, following outstanding Phase 3 clinical trial results that have energized market analysts and positioned the pharmaceutical giant to dominate the emerging oral GLP-1 sector. The successful trial outcomes effectively remove the final regulatory barrier and signal a potential paradigm shift in how obesity is treated globally.
Groundbreaking Clinical Results Pave Way for Approval
On August 26, 2025, Eli Lilly announced compelling topline data from its ATTAIN-2 Phase 3 study, which met all primary and secondary endpoints with remarkable efficacy. Participants receiving the high-dose regimen (36 mg daily) demonstrated an average weight reduction of 10.5% over 72 weeks, equivalent to nearly 23 pounds. The study additionally revealed significant improvements in blood glucose control, evidenced by a 1.8% reduction in A1C levels.
The safety profile remained consistent with established injectable GLP-1 medications, effectively addressing potential regulatory concerns. Company officials confirmed that all necessary clinical data for global regulatory submissions will be completed by year-end 2025, with obesity applications filed first followed by diabetes submissions in 2026.
Market Analysts Respond with Enthusiasm
The unequivocal trial success triggered immediate positive reactions across the analyst community. In a notable shift, Wall Street Zen upgraded Eli Lilly shares to “Strong Buy” on August 30, while HSBC had already revised its position days earlier, moving from “Reduce” to “Hold” and increasing its price target from $675 to $700. HSBC analyst Rajesh Kumar summarized the sentiment: “The bear case for Eli Lilly is effectively off the table.”
This development eliminated the final sell rating for the company’s stock. The conservative analyst consensus now sits at approximately $910, suggesting substantial upside potential from current trading levels.
Strategic Positioning in Massive Market Opportunity
The significance of Orforglipron’s development cannot be overstated within the context of the expanding GLP-1 market, projected to reach $150 billion over the next decade. While injectable formulations currently dominate, an effective oral alternative is expected to dramatically improve patient acceptance and enable global scalability.
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Kenneth Custer, Executive Vice President at Lilly, emphasized: “If approved, we will be ready to deliver a convenient, once-daily pill that can be scaled globally—breaking down barriers and redefining obesity treatment worldwide.”
Robust Financial Performance Supports Innovation
These pipeline advancements build upon already exceptional fundamental performance. Second-quarter 2025 results revealed revenue of $15.56 billion, representing 38% year-over-year growth. This expansion was primarily driven by blockbuster products Zepbound ($3.38 billion) and Mounjaro ($5.20 billion).
Management has raised full-year guidance to $60-62 billion in revenue, confirming sustained strength across all business segments. The company’s share of the US incretin market expanded to 57% during the quarter.
Upcoming Catalysts and Future Outlook
Investors are now focusing on several near-term catalysts, including third-quarter results scheduled for October 30, 2025, which will provide updated guidance and commentary on the Orforglipron regulatory timeline. The initiation of global regulatory filings later this year represents the next significant milestone.
Successful approvals would not only cement Eli Lilly’s leadership in diabetes and obesity treatments but potentially establish dominance in the entire oral GLP-1 sector. The convergence of a robust pipeline, exceptional financial performance, and strong analyst support creates a compelling investment thesis: Eli Lilly appears exceptionally well-positioned for its next growth phase.
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