Eli Lilly's Obesity Pill Orforglipron Gets FDA Clearance After Successful Trial
PorAinvest
martes, 26 de agosto de 2025, 1:09 pm ET1 min de lectura
LLY--
Eli Lilly and Company (LLY) has announced a significant milestone in its efforts to combat obesity, with its oral weight loss therapy, orforglipron, demonstrating substantial efficacy in a Phase 3 trial. The drug, a once-daily GLP-1 receptor agonist, has achieved its primary endpoint in the ATTAIN-2 trial, paving the way for global regulatory submissions [1].
The Phase 3 ATTAIN-2 trial, which involved 1,600 participants with obesity or overweight and at least one weight-related comorbidity, showed that orforglipron, when combined with a reduced-calorie diet and increased physical activity, led to an average weight loss of 22.9 pounds (10.5%) over 72 weeks at the highest dose [2]. This result surpasses the weight loss observed in previous trials of other weight loss medications, positioning orforglipron as a promising new treatment option in the global obesity crisis.
The safety profile of orforglipron was also evaluated during the trial. Common adverse events, such as nausea, diarrhea, and constipation, were generally mild to moderate in severity and resolved over time. No new safety signals were identified, indicating an acceptable overall safety profile for the drug [2].
With these positive results, Eli Lilly is now moving forward with global regulatory submissions for orforglipron. The company plans to submit applications to regulatory authorities in various regions, including the FDA. If approved, orforglipron could become a significant addition to the current landscape of weight loss treatments, offering a new oral option for individuals struggling with obesity or overweight.
The success of orforglipron in the Phase 3 trial underscores the ongoing efforts of pharmaceutical companies to develop effective and safe treatments for obesity. With the prevalence of obesity continuing to rise globally, innovative therapies like orforglipron are crucial for helping individuals achieve and maintain significant weight loss.
References:
[1] https://seekingalpha.com/news/4489112-eli-lilly-posts-phase-3-trial-win-obesity-pill
[2] https://www.ainvest.com/news/eli-lilly-orforglipron-achieves-10-5-weight-loss-phase-3-trial-2508/
Eli Lilly's obesity pill, orforglipron, has achieved the main goals in its third Phase 3 trial, allowing for global regulatory submissions. The once-daily GLP-1 receptor agonist is a potential treatment for weight loss. Lilly plans to submit the data to the FDA and other regulatory agencies.
Title: Eli Lilly's Orforglipron Achieves Phase 3 Trial Success, Advancing Global Regulatory SubmissionsEli Lilly and Company (LLY) has announced a significant milestone in its efforts to combat obesity, with its oral weight loss therapy, orforglipron, demonstrating substantial efficacy in a Phase 3 trial. The drug, a once-daily GLP-1 receptor agonist, has achieved its primary endpoint in the ATTAIN-2 trial, paving the way for global regulatory submissions [1].
The Phase 3 ATTAIN-2 trial, which involved 1,600 participants with obesity or overweight and at least one weight-related comorbidity, showed that orforglipron, when combined with a reduced-calorie diet and increased physical activity, led to an average weight loss of 22.9 pounds (10.5%) over 72 weeks at the highest dose [2]. This result surpasses the weight loss observed in previous trials of other weight loss medications, positioning orforglipron as a promising new treatment option in the global obesity crisis.
The safety profile of orforglipron was also evaluated during the trial. Common adverse events, such as nausea, diarrhea, and constipation, were generally mild to moderate in severity and resolved over time. No new safety signals were identified, indicating an acceptable overall safety profile for the drug [2].
With these positive results, Eli Lilly is now moving forward with global regulatory submissions for orforglipron. The company plans to submit applications to regulatory authorities in various regions, including the FDA. If approved, orforglipron could become a significant addition to the current landscape of weight loss treatments, offering a new oral option for individuals struggling with obesity or overweight.
The success of orforglipron in the Phase 3 trial underscores the ongoing efforts of pharmaceutical companies to develop effective and safe treatments for obesity. With the prevalence of obesity continuing to rise globally, innovative therapies like orforglipron are crucial for helping individuals achieve and maintain significant weight loss.
References:
[1] https://seekingalpha.com/news/4489112-eli-lilly-posts-phase-3-trial-win-obesity-pill
[2] https://www.ainvest.com/news/eli-lilly-orforglipron-achieves-10-5-weight-loss-phase-3-trial-2508/

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios