A Phase III Study to Assess the Effect of AZD0780 on LDL-C in Patients With Clinical ASCVD or at Risk for a First ASCVD Event

This is a study to evaluate the efficacy and safety of AZD0780 in adults with clinical ASCVD or who are at risk for a first ASCVD event and who have elevated LDL-C. AZD0780 is a small molecule that reduces the amount of LDL-C in the blood. Placebo will be used for comparison, and neither the participants nor the Investigators will know who is receiving the AZD0780 medication and who is receiving the placebo until the end of study. The total length of the study for an individual participant will be up to approximately 56 weeks, including a screening period of up to 14 days, treatment with AZD0780 or placebo for 52 weeks, and a safety follow-up period of 10 days.

NCT Number	NCT07000123
Lead Sponsor	AstraZeneca
Conditions	Cardiovascular Disease
Enrollment	3,103 participants
Start Date	2025-05-28
Primary Completion	2027-01-11 (estimated)
Study Completion	2027-01-11 (estimated)
Updated on ClinicalTrials.gov	2026-08-11