Olezarsen showed no significant difference versus placebo in noncalcified plaque volume change over 12 months in adults with moderate hypertriglyceridemia
A randomized, placebo-controlled trial evaluated olezarsen in 468 adults with largely moderate hypertriglyceridemia. Participants were followed for 12 months to assess changes in plaque volume. The primary outcome was the percent change from baseline to 12 months in noncalcified plaque volume. Secondary outcomes included changes in low-attenuation plaque volume, calcified plaque volume, and total plaque volume.
The analysis found that the percent change in noncalcified plaque volume did not differ between olezarsen and placebo. The 95% CI for this difference was -3.4 to 9.3 with a p-value of 0.36. No significant differences were observed for changes in low-attenuation, calcified, or total plaque volumes between the olezarsen and placebo groups.
Safety and tolerability data were not reported in the provided text. The study limitations were not reported. Given the lack of significant differences in plaque volume outcomes, the clinical relevance of olezarsen for this population remains uncertain based on these results.