Lilly touts results for once-daily weight-loss pill

The race to develop small-molecule alternatives to peptide-based weight-loss and antidiabetes drugs isn’t over, but a leader and a laggard have emerged. Eli Lilly and Company, which already markets weight-loss and diabetes drugs that must be injected, is a step closer to introducing a once-daily pill for the same conditions. On April 17, the company announced the results of a Phase 3 clinical trial of orforglipron, a small molecule that it licensed from the Japanese firm Chugai Pharmaceutical in 2018. The molecule functions as a glucagon-like peptide 1 (GLP-1) receptor agonist—using the same mode of action as the peptide-based injectables marketed by both Lilly and Novo Nordisk. In Lilly’s study, called Achieve-1, the company compared the safety and efficacy of orforglipron to those of a placebo in adults with type 2 diabetes and inadequate glycemic control who were on a diet and exercise regimen. According to Lilly’s press release, the

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Publication Details

Journal
C&EN Global Enterprise
Published
2025-04-28
DOI
https://doi.org/10.1021/cen-10311-buscon2
Primary Topic
Dietetics, Nutrition, and Education
Type
article
Field-Weighted Citation Impact
0.00
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article

Lilly touts results for once-daily weight-loss pill

Aayushi Pratap
C&EN Global Enterprise
Dietetics, Nutrition, and Education
article

Lilly touts results for once-daily weight-loss pill

Aayushi Pratap
article en

Abstract

The race to develop small-molecule alternatives to peptide-based weight-loss and antidiabetes drugs isn’t over, but a leader and a laggard have emerged. Eli Lilly and Company, which already markets weight-loss and diabetes drugs that must be injected, is a step closer to introducing a once-daily pill for the same conditions. On April 17, the company announced the results of a Phase 3 clinical trial of orforglipron, a small molecule that it licensed from the Japanese firm Chugai Pharmaceutical in 2018. The molecule functions as a glucagon-like peptide 1 (GLP-1) receptor agonist—using the same mode of action as the peptide-based injectables marketed by both Lilly and Novo Nordisk. In Lilly’s study, called Achieve-1, the company compared the safety and efficacy of orforglipron to those of a placebo in adults with type 2 diabetes and inadequate glycemic control who were on a diet and exercise regimen. According to Lilly’s press release, the

C&EN Global EnterpriseVol. 103(11)
Openalex Percentile: Top 90%
Dietetics, Nutrition, and Education
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