Eli Lilly And Company ((LLY)) announced an update on their ongoing clinical study.
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Study Overview: Eli Lilly and Company recently completed a study titled A Multiple-Dose Study to Investigate the Bioequivalence of Orforglipron (LY3502970) Capsules and Orforglipron Tablets in Participants With Obesity or Overweight Who Are Otherwise Healthy. The study aimed to compare how Orforglipron, a drug intended for overweight and obese individuals, is absorbed and processed in the body when administered as capsules versus tablets. The research also assessed the safety and tolerability of the drug in these forms.
Intervention/Treatment: The study tested Orforglipron, an orally administered drug. Participants received different sequences of Orforglipron doses as either tablets or capsules to evaluate its bioavailability and bioequivalence.
Study Design: This Phase 1 interventional study was randomized with a parallel assignment model. It was unmasked, meaning both participants and researchers knew which form of the drug was being administered. The primary purpose was to gather basic scientific data on the drug’s bioequivalence.
Study Timeline: The study began on June 24, 2024, and was last updated on June 23, 2025. These dates are crucial as they mark the progression and completion of the study, providing a timeline for data collection and analysis.
Market Implications: The completion of this study could positively influence Eli Lilly’s stock performance by demonstrating the potential effectiveness and flexibility of Orforglipron in different forms. This could enhance investor confidence, especially as the company competes in the growing market for obesity treatments.
The study is completed, and further details are available on the ClinicalTrials portal.