drugset / Trial / NCT03361501

A Phase 3 STudy of CaPRe in LOwering Very hiGh TriglYcerides (TRILOGY 2)

NCT03361501 ↗

Phase 3 Completed 278 enrolled Grace Therapeutics Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to determine the efficacy of CaPre 4 g daily, compared to placebo, in lowering fasting TG levels in subjects with fasting TG levels ≥500 mg/dL and ≤1500 mg/dL (≥5.7 mmol/L and ≤17.0 mmol/L) after 12 weeks of treatment. Approximately 615 subjects will be screened to obtain 245 randomized subjects following a treatment allocation ratio of 2.5:1 (CaPre:placebo).

Timeline

Start
2018-02-01
Primary completion
2019-09-24
Completion
2020-01-09

Outcome

Met primary endpoint

paper mean treatment difference, -10.9% [95% CI, -20.4% to -1.5%]; P = .02 PMID 34989797 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject CaPre Other / unclassified 4 g Oral

Indications