U.S., Nov. 4 -- ClinicalTrials.gov registry received information related to the study (NCT07223593) titled 'Efficacy and Safety of Orforglipron in Participants With Peripheral Artery Disease' on Oct. 30.
Brief Summary: The purpose of this study is to evaluate the effect and safety of orforglipron once daily in participants with Fontaine II peripheral arterial disease (PAD). Participation in the study will last about 58 weeks.
Study Start Date: Dec., 2025
Study Type: INTERVENTIONAL
Condition:
Peripheral Arterial Disease
Intervention:
DRUG: Orforglipron
Administered orally
DRUG: Placebo
Administered orally
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Eli Lilly and Company
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