drugset / Trial / NCT03361501
A Phase 3 STudy of CaPRe in LOwering Very hiGh TriglYcerides (TRILOGY 2)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CaPre | Other / unclassified | 4 g | Oral |