Lipids & metabolic liver disease

Efficacy and Safety of Olezarsen in Hypertriglyceridemia: An Updated Meta‐Analysis of Randomised Controlled Trials

Diabetes Obes MetabPublished Systematic review and meta-analysis of randomised controlled trials

Authors' conclusion

Olezarsen provides substantial triglyceride reduction with favourable effects on atherogenic lipoproteins and a tolerable short-term safety profile. Longer-term trials are needed to confirm cardiovascular outcomes and safety.

Study context

Population
Patients with hypertriglyceridemia in randomised controlled trials (RCTs) (PubMed, Cochrane, Scopus, Web of Science up to December 2025)
Participants
2,676 patients6 RCTs
Comparison
Olezarsen vs placebo
Outcome
Triglycerides, mean percentage change
Methodological detailsrandom-effects models
  • Random-effects models

Pooled result

As reported in the abstract

Each group vs placeboMD, % (95% CI)P value
Olezarsen 50 mg
−46.61(−49.59 to −43.64)
P < 0.0001
Olezarsen 80 mg
−54.37(−61.26 to −47.48)
P < 0.0001

Further pooled results

OutcomeMD (%) (95% CI)P value
ApoC-III, mean % change50 mgvs Placebo−63.51 (−74.18 to −52.84)P < 0.0001
ApoC-III, mean % change80 mgvs Placebo−66.88 (−77.91 to −55.85)P < 0.0001
Non-HDL-C, mean % change50 mgvs Placebo−21.41 (−25.12 to −17.70)P < 0.0001
Non-HDL-C, mean % change80 mgvs Placebo−25.28 (−33.99 to −16.58)P = 0.001
LDL-C, mean % change50 mgvs Placebo17.58 (0.24–34.93)P = 0.047
OutcomeRR (95% CI)P value
Acute pancreatitis50 mgvs Placebo0.16 (0.05–0.48)P = 0.001
Acute pancreatitis80 mgvs Placebo0.33 (0.14–0.76)P = 0.009

Safety

OutcomeRR (95% CI)P value
ALT/AST ≥ 3 × ULNOlezarsen 80 mgvs Placebo2.56 (1.20–5.44)P = 0.01

Overall adverse events

Overall adverse events comparable to placebo

Original publication

Efficacy and Safety of Olezarsen in Hypertriglyceridemia: An Updated Meta‐Analysis of Randomised Controlled Trials. Diabetes Obes Metab. Published 7 April 2026. doi:10.1111/dom.70716

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