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Clinical Trials in the EU / 2025-521117-88-00
Completed Phase III

A Double-blind, Randomized, Placebo-controlled, Multi-center Study Evaluating the Safety, Tolerability, and Effect of Olpasiran on Coronary Artery Plaque Burden Assessed by Coronary Computed Tomography Angiography in Participants With Stable Atherosclerotic Cardiovascular Disease and Elevated Lipoprotein(a)

2025-521117-88-00 · tracked via the Priya Life Science EU tracker
Sponsor
Amgen Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Cardiovascular Diseases
Decision date
22/12/2025
Enrollment target
178
Sites
France, Denmark, Germany, Spain, Italy, Netherlands

Condition studied

Cardiovascular Disease

Investigational medicinal product(s)

Placebo for AMG 890Olpasiran

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

change in non-calcified plaque volume from baseline to week 72

Endpoint detail

change in the following volume types from baseline to week 72: -low attenuation plaque volume -total plaque volume -calcified plaque volume

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-521117-88-00 on CTIS ↗ ← All trials in the EU