A Study of Olezarsen Administered Subcutaneously to Participants With Severe Hypertriglyceridemia
Purpose
The purpose of this study is to evaluate the efficacy of olezarsen as compared to placebo on the percent change in fasting triglycerides (TG) from baseline.
Condition
- Severe Hypertriglyceridemia
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Fasting TG ≥ 500 mg/dL (5.65 mmol/L) at Screening and Qualification 2. Participants must be on lipid-lowering therapy that should adhere to standard of care (SOC) per local guidelines. Lipid-lowering medications should be optimized and stabilized for at least 4 weeks prior to screening to minimize changes in these medications during the study. 3. Participants must be willing to comply with diet and lifestyle recommendations as able.
Exclusion Criteria
- Hemoglobin A1c (HbA1c) ≥ 9.5% at Screening 2. Alanine aminotransferase or aspartate aminotransferase > 3.0 × upper limit of normal 3. Total bilirubin > 1.5 ULN unless due to Gilbert's syndrome 4. Estimated GFR < 30 mL/min/1.73 m^2
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Care Provider, Investigator)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Olezarsen |
Olezarsen will be administered once every 4 weeks by subcutaneous (SC) injection from Week 1 through Week 49. |
|
|
Placebo Comparator Placebo |
Olezarsen-matching placebo will be administered once every 4 weeks by subcutaneous (SC) injection from Week 1 through Week 49. |
|
More Details
- Status
- Completed
- Sponsor
- Ionis Pharmaceuticals, Inc.
Study Contact
Detailed Description
This is a Phase 3, multi-center, randomized, double-blind, placebo-controlled study in 446 participants. Participants will be randomized to receive olezarsen or placebo in a 53-week treatment period. The length of participation in the study will be approximately 78 weeks, which includes an up to 12-week screening period, a 53-week treatment period, and a 13-week post-treatment evaluation period or transition to open-label extension (OLE) study with up to 1-year treatment.